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  <title>The BioInsights Podcast</title>

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  <description><![CDATA[The BioInsights Podcast: discussing the challenges of translating novel biologics from bench to clinic to market.]]></description>
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    <itunes:title>From one target to many: how high‑plex ddPCR is changing CGT from development to analytics</itunes:title>
    <title>From one target to many: how high‑plex ddPCR is changing CGT from development to analytics</title>
    <itunes:summary><![CDATA[Lauren Coyle, Editor, BioInsights, speaks with Christian Overgaard, Senior Field Application Scientist, Bio‑Rad Laboratories, about the technical and practical evolution of droplet digital PCR (ddPCR) and high‑plex multiplexing, covering assay design challenges, vector integration analysis, biodistribution studies, and the emerging role of digital PCR in cell and gene therapy characterization and clinical development. ]]></itunes:summary>
    <description><![CDATA[<p>Lauren Coyle, Editor, BioInsights, speaks with Christian Overgaard, Senior Field Application Scientist, Bio‑Rad Laboratories, about the technical and practical evolution of droplet digital PCR (ddPCR) and high‑plex multiplexing, covering assay design challenges, vector integration analysis, biodistribution studies, and the emerging role of digital PCR in cell and gene therapy characterization and clinical development.</p>]]></description>
    <content:encoded><![CDATA[<p>Lauren Coyle, Editor, BioInsights, speaks with Christian Overgaard, Senior Field Application Scientist, Bio‑Rad Laboratories, about the technical and practical evolution of droplet digital PCR (ddPCR) and high‑plex multiplexing, covering assay design challenges, vector integration analysis, biodistribution studies, and the emerging role of digital PCR in cell and gene therapy characterization and clinical development.</p>]]></content:encoded>
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    <itunes:author>BioInsights</itunes:author>
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    <pubDate>Wed, 24 Jun 2026 08:00:00 +0000</pubDate>
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  <psc:chapter start="0:00" title="From one target to many: how high‑plex ddPCR is changing CGT from development to analytics" />
  <psc:chapter start="1:17" title="1.	Multiplexing in qPCR has long been considered technically challenging to scale reliably. What are the underlying reasons for this?" />
  <psc:chapter start="2:11" title="2.	Droplet digital PCR (ddPCR) operates on a fundamentally different principle. Can you explain the distinction, and how does that change what is achievable in higher-plex assay design?" />
  <psc:chapter start="3:49" title="3.	Where do labs typically encounter limitations when trying to operationalize high-plex workflows?" />
  <psc:chapter start="5:25" title="4.	How did workflow speed previously limit gene expression studies? a.	5.25" />
  <psc:chapter start="6:48" title="5.	Why is copy number alone insufficient for cell therapy characterization?" />
  <psc:chapter start="8:12" title="Vector integration analysis has historically relied on complex long-range assays. How does a small amplicon multiplexing approach change that in practice?" />
  <psc:chapter start="10:40" title="7.	Biodistribution studies typically involve a large number of targets across multiple tissue types. What does high-plex gene expression profiling make possible that previously was not feasible at scale?" />
  <psc:chapter start="11:35" title="There appears to be a broader shift towards using next-generation sequencing (NGS) for discovery and ddPCR for longitudinal monitoring. Is this a pattern you are observing, and what do you think is driving it?" />
  <psc:chapter start="12:47" title="As multiplexing capacity continues to develop, where do you see the most meaningful advances coming from?" />
</psc:chapters>
    <itunes:duration>925</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>5</itunes:season>
    <itunes:episode>4</itunes:episode>
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    <itunes:title>Beyond one and done: engineering durable, redosable cell‑based gene therapies</itunes:title>
    <title>Beyond one and done: engineering durable, redosable cell‑based gene therapies</title>
    <itunes:summary><![CDATA[The one‑and‑done model has defined gene therapy for a generation. Chris Hopkins thinks it is time to move on. At ASGCT 2026, Abi Pinchbeck spoke with the Co‑founder and CEO of Glafabra Therapeutics on redoseable cell‑based gene therapy, a platform spanning Fabry, Pompe, and Gaucher diseases, and what durable, if not permanent, treatment could mean for patients. A podcast version of this discussion is also available. ]]></itunes:summary>
    <description><![CDATA[<p>The one‑and‑done model has defined gene therapy for a generation. Chris Hopkins thinks it is time to move on. At ASGCT 2026, Abi Pinchbeck spoke with the Co‑founder and CEO of Glafabra Therapeutics on redoseable cell‑based gene therapy, a platform spanning Fabry, Pompe, and Gaucher diseases, and what durable, if not permanent, treatment could mean for patients. A podcast version of this discussion is also available.</p>]]></description>
    <content:encoded><![CDATA[<p>The one‑and‑done model has defined gene therapy for a generation. Chris Hopkins thinks it is time to move on. At ASGCT 2026, Abi Pinchbeck spoke with the Co‑founder and CEO of Glafabra Therapeutics on redoseable cell‑based gene therapy, a platform spanning Fabry, Pompe, and Gaucher diseases, and what durable, if not permanent, treatment could mean for patients. A podcast version of this discussion is also available.</p>]]></content:encoded>
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    <itunes:author>BioInsights</itunes:author>
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    <pubDate>Wed, 17 Jun 2026 09:00:00 +0000</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="Beyond one and done: engineering durable, redosable cell‑based gene therapies" />
  <psc:chapter start="1:43:00" title="Fabry disease has traditionally been managed with enzyme replacement therapy. What led you to pursue a cell‑based gene therapy approach for this indication?" />
  <psc:chapter start="3:19:00" title="Redosability is central to your platform. How central was it as a design principle from the outset, and what does it mean for how clinicians are likely to schedule treatment?" />
  <psc:chapter start="7:46:00" title="How do you think about the trade‑offs between gene addition and in situ editing for lysosomal storage diseases, and does a redosable design change that decision‑making?" />
  <psc:chapter start="9:27:00" title="After Fabry disease, you have identified Pompe and Gaucher diseases as the next targets. What is the rationale for that expansion?" />
  <psc:chapter start="10:52:00" title="Where do each of your three programs currently stand, and what is your regulatory strategy for each?" />
  <psc:chapter start="14:14:00" title="What does the right pharma or biotech partnership look like, and at what stage does that conversation become most productive?" />
  <psc:chapter start="16:26:00" title="Finally, where do you see the company in the next five years, and what would it mean for patients?" />
</psc:chapters>
    <itunes:duration>1114</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>5</itunes:season>
    <itunes:episode>3</itunes:episode>
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    <itunes:title>Precision by design: engineering site‑specific ADCs with machine learning</itunes:title>
    <title>Precision by design: engineering site‑specific ADCs with machine learning</title>
    <itunes:summary><![CDATA[Lauren Coyle, Launch Commissioning Editor, Bioconjugate Insights, speaks with Weston Kightlinger, CEO, Ridge Bio, about the challenge of DAR heterogeneity and site specificity in ADC development, Ridge Bio’s ML‑driven enzyme and linker engineering platforms, and what site‑specific conjugation means for the future of ADCs as the field moves beyond oncology. ]]></itunes:summary>
    <description><![CDATA[<p>Lauren Coyle, Launch Commissioning Editor, Bioconjugate Insights, speaks with Weston Kightlinger, CEO, Ridge Bio, about the challenge of DAR heterogeneity and site specificity in ADC development, Ridge Bio’s ML‑driven enzyme and linker engineering platforms, and what site‑specific conjugation means for the future of ADCs as the field moves beyond oncology.</p>]]></description>
    <content:encoded><![CDATA[<p>Lauren Coyle, Launch Commissioning Editor, Bioconjugate Insights, speaks with Weston Kightlinger, CEO, Ridge Bio, about the challenge of DAR heterogeneity and site specificity in ADC development, Ridge Bio’s ML‑driven enzyme and linker engineering platforms, and what site‑specific conjugation means for the future of ADCs as the field moves beyond oncology.</p>]]></content:encoded>
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    <itunes:author>BioInsights</itunes:author>
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    <pubDate>Thu, 21 May 2026 16:00:00 +0000</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="Precision by design: engineering site‑specific ADCs with machine learning" />
  <psc:chapter start="1:17" title="1.	Site specificity has been a persistent challenge in ADC development, with issues such as DAR heterogeneity, unpredictable conjugation, and batch variability. From your position, how significant is this problem in practice and why has it proven so diffi" />
  <psc:chapter start="5:44" title="2.	Ridge Bio sits at an unusual intersection of machine learning (ML), cell-free experimentation, and enzyme engineering. Can you walk us through how these three elements work together in practice, and what this combination allows you to do that conventio" />
  <psc:chapter start="10:01" title="3.	Ridge&#39;s NativeLink and ProTrigger platforms span ADCs, antibody-oligonucleotide conjugates (AOCs), radiotherapies, and beyond. How do you think about the relationship between enzymatic conjugation precision and linker release design as integrated rathe" />
  <psc:chapter start="13:18" title="4.	Platform science is one thing, but can you give us a sense of the real problems being solved today, the programs that NativeLink and ProTrigger are being applied to, and what the partnership experience has revealed about where the technology adds the m" />
  <psc:chapter start="17:03" title="5.	ML in drug development carries significant promise, but also genuine skepticism, particularly around whether models trained on existing data can navigate the novel chemical and biological spaces that next-generation ADCs require. How do you address tha" />
  <psc:chapter start="19:47" title="6.	How does Ridge expect site-specific conjugation to impact the future of ADCs, especially as the field begins to push outside of oncology, and what needs to happen – technically or commercially – to establish ML-driven enzyme engineering as the field&#39;s " />
</psc:chapters>
    <itunes:duration>1468</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>5</itunes:season>
    <itunes:episode>2</itunes:episode>
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    <itunes:title>Crossing the ADC inflection points: what separates clinical success from failure</itunes:title>
    <title>Crossing the ADC inflection points: what separates clinical success from failure</title>
    <itunes:summary><![CDATA[Lauren Coyle, Launch Commissioning Editor, Bioconjugate Insights, speaks with Antoine Yver, Board Chair, Ona Therapeutics, with more than three and a half decades of experience shaping global cancer drug development. In this conversation, they explore what determines whether an ADC successfully crosses the critical threshold and how teams should rethink dose finding, toxicity, and what it truly takes to set a program up for long-term success in the clinic.  ]]></itunes:summary>
    <description><![CDATA[<p>Lauren Coyle, Launch Commissioning Editor, <em>Bioconjugate Insights</em>, speaks with Antoine Yver, Board Chair, Ona Therapeutics, with more than three and a half decades of experience shaping global cancer drug development. In this conversation, they explore what determines whether an ADC successfully crosses the critical threshold and how teams should rethink dose finding, toxicity, and what it truly takes to set a program up for long-term success in the clinic. </p>]]></description>
    <content:encoded><![CDATA[<p>Lauren Coyle, Launch Commissioning Editor, <em>Bioconjugate Insights</em>, speaks with Antoine Yver, Board Chair, Ona Therapeutics, with more than three and a half decades of experience shaping global cancer drug development. In this conversation, they explore what determines whether an ADC successfully crosses the critical threshold and how teams should rethink dose finding, toxicity, and what it truly takes to set a program up for long-term success in the clinic. </p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/18731065-crossing-the-adc-inflection-points-what-separates-clinical-success-from-failure.mp3" length="21712087" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
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    <pubDate>Mon, 23 Feb 2026 17:00:00 +0000</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="Crossing the ADC inflection points: what separates clinical success from failure" />
  <psc:chapter start="1:12" title="1.	You have led multiple oncology programs from discovery to approval. What do you see as the most critical translational inflection points, when looking specifically at ADCs, that determine whether a molecule successfully crosses the ‘bench-to-bedside’ t" />
  <psc:chapter start="5:44" title="2.	ADCs often present atypical toxicity profiles and non-linear response kinetics. How should early development teams rethink dose-finding and safety management strategies to avoid applying conventional monoclonal antibody or small-molecule paradigms that" />
  <psc:chapter start="12:47" title="3.	As payloads diversify and mechanisms evolve, what do you consider the most appropriate early clinical endpoints to convincingly demonstrate mechanistic value and accelerate early go/no-go decisions?  " />
  <psc:chapter start="15:39" title="4.	For modern ADCs, what level of biomarker maturity or target-expression characterization is truly required before entering first-in-human studies?  " />
  <psc:chapter start="17:18" title="5.	Preparing an IND for a first-in-class ADC places enormous pressure on analytical, CMC, and scalability planning. From your experience, what defines ‘IND-readiness,’ and what common CMC missteps most often jeopardize smooth progression into GMP manufact" />
  <psc:chapter start="22:03" title="6.	Translating ADCs into the clinic increasingly requires seamless integration of discovery workflows with GMP-compatible conjugation and scale up. What operational principles or lessons learned from past programs do you believe are essential for avoiding" />
  <psc:chapter start="25:26" title="7.	Lastly, what single innovation, whether technical, biological, or regulatory, would most profoundly improve the success rates of ADCs entering the clinic over the next decade?  " />
</psc:chapters>
    <itunes:duration>1806</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>5</itunes:season>
    <itunes:episode>1</itunes:episode>
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    <itunes:title>Formulation and delivery of RNA-based vaccines and therapeutics: addressing outstanding questions around safety and purity</itunes:title>
    <title>Formulation and delivery of RNA-based vaccines and therapeutics: addressing outstanding questions around safety and purity</title>
    <itunes:summary><![CDATA[In this interview, Róisin McGuigan, Editor, Nucleic Acid Insights, and Jesse Erasmus, Director of Virology at HDT Bio, discuss current challenges and opportunities in RNA safety, manufacturing, and targeted delivery, and the key ongoing obstacles facing viral and LNP-based delivery modalities. ]]></itunes:summary>
    <description><![CDATA[<p>In this interview, <b>Róisin McGuigan</b>, Editor, <em>Nucleic Acid Insights</em>, and <b>Jesse Erasmus</b>, Director of Virology at HDT Bio, discuss current challenges and opportunities in RNA safety, manufacturing, and targeted delivery, and the key ongoing obstacles facing viral and LNP-based delivery modalities.</p>]]></description>
    <content:encoded><![CDATA[<p>In this interview, <b>Róisin McGuigan</b>, Editor, <em>Nucleic Acid Insights</em>, and <b>Jesse Erasmus</b>, Director of Virology at HDT Bio, discuss current challenges and opportunities in RNA safety, manufacturing, and targeted delivery, and the key ongoing obstacles facing viral and LNP-based delivery modalities.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/18144826-formulation-and-delivery-of-rna-based-vaccines-and-therapeutics-addressing-outstanding-questions-around-safety-and-purity.mp3" length="17582922" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
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    <pubDate>Thu, 06 Nov 2025 17:00:00 +0000</pubDate>
    <itunes:duration>1462</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>4</itunes:season>
    <itunes:episode>8</itunes:episode>
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    <itunes:title>Advancing nucleic acid therapeutics with circular RNA</itunes:title>
    <title>Advancing nucleic acid therapeutics with circular RNA</title>
    <itunes:summary><![CDATA[In this podcast episode, Jokūbas Leikauskas, Editor, BioInsights, speaks to Trevor Hallam, who served as Chief Scientific Officer of Sail Biomedicines until July 2025. The interview, recorded in June 2025, explores advances in RNA therapeutics, particularly circular RNA (circRNA or eRNA) technologies, and how they may help overcome current limitations in delivery, durability, and specificity for applications such as CAR-T cell therapies and autoimmune disease treatment. ]]></itunes:summary>
    <description><![CDATA[<p>In this podcast episode, <b>Jokūbas Leikauskas</b>, Editor, BioInsights, speaks to <b>Trevor Hallam</b>, who served as Chief Scientific Officer of Sail Biomedicines until July 2025. The interview, recorded in June 2025, explores advances in RNA therapeutics, particularly circular RNA (circRNA or eRNA) technologies, and how they may help overcome current limitations in delivery, durability, and specificity for applications such as CAR-T cell therapies and autoimmune disease treatment.</p>]]></description>
    <content:encoded><![CDATA[<p>In this podcast episode, <b>Jokūbas Leikauskas</b>, Editor, BioInsights, speaks to <b>Trevor Hallam</b>, who served as Chief Scientific Officer of Sail Biomedicines until July 2025. The interview, recorded in June 2025, explores advances in RNA therapeutics, particularly circular RNA (circRNA or eRNA) technologies, and how they may help overcome current limitations in delivery, durability, and specificity for applications such as CAR-T cell therapies and autoimmune disease treatment.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/18081099-advancing-nucleic-acid-therapeutics-with-circular-rna.mp3" length="24400584" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
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    <pubDate>Mon, 27 Oct 2025 12:00:00 +0000</pubDate>
    <itunes:duration>2027</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>4</itunes:season>
    <itunes:episode>7</itunes:episode>
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    <itunes:title>Exploring advances in bioconjugation: nanozymes, tissue tropism, and the future of responsive systems</itunes:title>
    <title>Exploring advances in bioconjugation: nanozymes, tissue tropism, and the future of responsive systems</title>
    <itunes:summary><![CDATA[Lauren Coyle (Commissioning Editor, Bioconjugation Insights) speaks to Vincent Rotello (Distinguished Professor of Chemistry, University of Massachusetts Amherst) about the advantages and limitations of different nanomaterial platforms, and emerging strategies such as tissue tropism and responsive nanozymes that could advance targeted therapeutic and diagnostic delivery. ]]></itunes:summary>
    <description><![CDATA[<p><b>Lauren Coyle</b> (Commissioning Editor, <em>Bioconjugation Insights</em>) speaks to <b>Vincent Rotello</b> (Distinguished Professor of Chemistry, University of Massachusetts Amherst) about the advantages and limitations of different nanomaterial platforms, and emerging strategies such as tissue tropism and responsive nanozymes that could advance targeted therapeutic and diagnostic delivery.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Lauren Coyle</b> (Commissioning Editor, <em>Bioconjugation Insights</em>) speaks to <b>Vincent Rotello</b> (Distinguished Professor of Chemistry, University of Massachusetts Amherst) about the advantages and limitations of different nanomaterial platforms, and emerging strategies such as tissue tropism and responsive nanozymes that could advance targeted therapeutic and diagnostic delivery.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/17938523-exploring-advances-in-bioconjugation-nanozymes-tissue-tropism-and-the-future-of-responsive-systems.mp3" length="11192668" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
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    <pubDate>Wed, 01 Oct 2025 14:00:00 +0000</pubDate>
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  <psc:chapter start="0:00" title="Exploring advances in bioconjugation: nanozymes, tissue tropism, and the future of responsive systems" />
  <psc:chapter start="1:18" title="I thought we could start with you telling us a bit about your journey into bioconjugation research. What initially drew you into the field?" />
  <psc:chapter start="3:48" title="While ADCs have captured much of the spotlight, the field extends far beyond these. What other areas of bioconjugation do you see as particularly promising or underappreciated?" />
  <psc:chapter start="5:45" title="What unique advantages do nanomaterials offer as platforms for bioconjugation compared to more traditional approaches?" />
  <psc:chapter start="7:54" title="What are some key challenges in achieving stable, functional conjugation at nanoscale? " />
  <psc:chapter start="9:46" title="Could you provide some examples of how engineered nanomaterial conjugates are being developed for therapeutic or diagnostic applications?" />
  <psc:chapter start="11:30" title="What emerging nanomaterial platforms or conjugation strategies are you most excited about, and have any recent breakthroughs in surface chemistry opened new possibilities for nanomaterial-based conjugates?" />
  <psc:chapter start="13:15" title="Looking ahead, what technological advances or breakthroughs do you think will drive the field forward over the next 5-10 years, and how might this impact research and/or clinical applications?" />
</psc:chapters>
    <itunes:duration>929</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>4</itunes:season>
    <itunes:episode>6</itunes:episode>
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    <itunes:title>The promise of antibody-oligonucleotide conjugates for neurological diseases</itunes:title>
    <title>The promise of antibody-oligonucleotide conjugates for neurological diseases</title>
    <itunes:summary><![CDATA[Lauren Coyle, Launch Commissioning Editor, Bioconjugation Insights, speaks with Kerstin Hofer, Science and People Lead, Roche, about the evolving application of antibody-oligonucleotide conjugates in neurology. She highlights their design, delivery challenges across the blood–brain barrier, and potential to transform CNS diseases. ]]></itunes:summary>
    <description><![CDATA[<p><b>Lauren Coyle</b>, Launch Commissioning Editor, <em>Bioconjugation Insights</em>, speaks with <b>Kerstin Hofer</b>, Science and People Lead, Roche, about the evolving application of antibody-oligonucleotide conjugates in neurology. She highlights their design, delivery challenges across the blood–brain barrier, and potential to transform CNS diseases.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Lauren Coyle</b>, Launch Commissioning Editor, <em>Bioconjugation Insights</em>, speaks with <b>Kerstin Hofer</b>, Science and People Lead, Roche, about the evolving application of antibody-oligonucleotide conjugates in neurology. She highlights their design, delivery challenges across the blood–brain barrier, and potential to transform CNS diseases.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/17741349-the-promise-of-antibody-oligonucleotide-conjugates-for-neurological-diseases.mp3" length="15430488" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
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    <pubDate>Wed, 27 Aug 2025 09:00:00 +0000</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="The promise of antibody-oligonucleotide conjugates for neurological diseases" />
  <psc:chapter start="1:07" title="What inspired your interest in exploring the translation of ADCs, which are traditionally oncology-focused, and moving them into this field? " />
  <psc:chapter start="4:37" title="Would you be able to give more details on how these AOCs differ from ADCs and what makes them particularly exciting for neurological applications? " />
  <psc:chapter start="6:55" title="One of the biggest challenges in treating brain disorders is the BBB. How are you and your team approaching the challenge of getting AOCs across this barrier, and are there particular delivery technologies or strategies that you have been excited about? " />
  <psc:chapter start="10:12" title="What do you think are the key design elements, such as conjugation techniques or linker chemistries, that impact success in AOC design and development? " />
  <psc:chapter start="14:38" title="Following on from this, what unique hurdles do AOCs face in the neurological space that perhaps aren&#39;t as prominent in oncology? " />
  <psc:chapter start="18:24" title="Finally, as the field of AOCs grows, what advancements or breakthroughs do you think are needed to fully unlock therapeutic potential in the brain? " />
</psc:chapters>
    <itunes:duration>1282</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>4</itunes:season>
    <itunes:episode>5</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>From innovation to access: bridging gaps in scalability and cold chain precision logistics for advanced therapies</itunes:title>
    <title>From innovation to access: bridging gaps in scalability and cold chain precision logistics for advanced therapies</title>
    <itunes:summary><![CDATA[Jokūbas Leikauskas, Editor, BioInsights, speaks to Rohin Iyer, Senior Director, Global Cell and Gene Therapy Operations, Marken, about addressing the complex logistics of cell and gene therapies through global infrastructure, precision, and advanced technologies. They also discuss evolving cold chain needs, regulatory and geopolitical challenges, and the need for scalability.    ]]></itunes:summary>
    <description><![CDATA[<p><b>Jokūbas Leikauskas</b>, Editor, BioInsights, speaks to <b>Rohin Iyer</b>, Senior Director, Global Cell and Gene Therapy Operations, Marken, about addressing the complex logistics of cell and gene therapies through global infrastructure, precision, and advanced technologies. They also discuss evolving cold chain needs, regulatory and geopolitical challenges, and the need for scalability. <br/><br/></p>]]></description>
    <content:encoded><![CDATA[<p><b>Jokūbas Leikauskas</b>, Editor, BioInsights, speaks to <b>Rohin Iyer</b>, Senior Director, Global Cell and Gene Therapy Operations, Marken, about addressing the complex logistics of cell and gene therapies through global infrastructure, precision, and advanced technologies. They also discuss evolving cold chain needs, regulatory and geopolitical challenges, and the need for scalability. <br/><br/></p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/17521249-from-innovation-to-access-bridging-gaps-in-scalability-and-cold-chain-precision-logistics-for-advanced-therapies.mp3" length="14329750" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-17521249</guid>
    <pubDate>Fri, 18 Jul 2025 10:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/17521249/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="From innovation to access: bridging gaps in scalability and cold chain precision logistics for advanced therapies" />
  <psc:chapter start="1:19" title="Starting with Marken’s role in the CGT ecosystem, how does your team support the unique logistic needs of CGT’s, particularly when it comes to ensuring global delivery of uncompromised product integrity?" />
  <psc:chapter start="2:47" title="Following on, what recent innovations or regulatory shifts are having the biggest impact on how CGTs are developed, transported, and delivered?" />
  <psc:chapter start="5:58" title="As the complexity of CGT logistics continues to grow, what are the most pressing bottlenecks or vulnerabilities of today’s cold chain infrastructure and how can we start to solve them?" />
  <psc:chapter start="8:13" title="With this in mind, how does Marken define precision in this context, and what technologies or process are central to achieving that level of control, visiblity, and responsiveness?" />
  <psc:chapter start="12:05" title="Scale is often a limiting factor for emerging therapies. What does scalable logistics look like in the CGT space, especially when dealing with personalized patient specific treatment across boarders?" />
  <psc:chapter start="15:34" title="Looking ahead, the CGT pipeline is only getting more crowded and complex. What disruptions do you foresee over the next 3-5 years, and how is Marken evolving to stay ahead of those changes?" />
</psc:chapters>
    <itunes:duration>1189</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>4</itunes:season>
    <itunes:episode>4</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Enhancing mRNA results through strategic RNA design and quality control</itunes:title>
    <title>Enhancing mRNA results through strategic RNA design and quality control</title>
    <itunes:summary><![CDATA[In the last few years, mRNA has moved to the fore in the vaccine and cell and gene therapy fields, and as a result, its successful production for these downstream applications has never been more crucial. In this podcast episode, Róisin McGuigan, Editor, Nucleic Acid Insights, speaks to Ryan Lahr, Senior R&amp;D Scientist, CELLSCRIPT, about design, production, and quality control of synthesized mRNA for translation in cells.   ]]></itunes:summary>
    <description><![CDATA[<p>In the last few years, mRNA has moved to the fore in the vaccine and cell and gene therapy fields, and as a result, its successful production for these downstream applications has never been more crucial. In this podcast episode, <b>Róisin McGuigan</b>, Editor, <em>Nucleic Acid Insights</em>, speaks to <b>Ryan Lahr</b>, Senior R&amp;D Scientist, CELLSCRIPT, about design, production, and quality control of synthesized mRNA for translation in cells.<br/><br/></p>]]></description>
    <content:encoded><![CDATA[<p>In the last few years, mRNA has moved to the fore in the vaccine and cell and gene therapy fields, and as a result, its successful production for these downstream applications has never been more crucial. In this podcast episode, <b>Róisin McGuigan</b>, Editor, <em>Nucleic Acid Insights</em>, speaks to <b>Ryan Lahr</b>, Senior R&amp;D Scientist, CELLSCRIPT, about design, production, and quality control of synthesized mRNA for translation in cells.<br/><br/></p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/16834381-enhancing-mrna-results-through-strategic-rna-design-and-quality-control.mp3" length="9322823" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-16834381</guid>
    <pubDate>Thu, 27 Mar 2025 11:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/16834381/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Enhancing mRNA results through strategic RNA design and quality control" />
  <psc:chapter start="1:27" title="Can you tell me a bit about yourself and the current work that you do? " />
  <psc:chapter start="2:21" title="Can you frame for us the key challenges and considerations when optimizing mRNA design for different research applications in the vaccine and cell and gene therapy fields? " />
  <psc:chapter start="4:53" title="Can you expand on the impact design decisions around nucleoside composition, cap structure and length of poly(A) tail have, on both the quality and functionality of mRNA? " />
  <psc:chapter start="6:36" title="And looking at immunity, how can the risk of innate immunity development best be addressed? " />
  <psc:chapter start="9:03" title="What advice would you share with developers looking to optimize mRNA design and synthesis for their own specific application? " />
  <psc:chapter start="9:56" title="What are the key considerations and common pitfalls when developing a quality control strategy for synthesized transcripts? What analytical tools and techniques are available to assess the quality of mRNA transcripts?  " />
  <psc:chapter start="11:41" title="And finally, what advice would you give to new researchers interested in using mRNA for translation in cells? " />
</psc:chapters>
    <itunes:duration>773</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>4</itunes:season>
    <itunes:episode>3</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>For the many and the few: bringing ASO therapies to both mainstream and nano-rare indications</itunes:title>
    <title>For the many and the few: bringing ASO therapies to both mainstream and nano-rare indications</title>
    <itunes:summary><![CDATA[Roisin McGuigan, Commissioning Editor, Nucleic Acid Insights, speaks to Stanley Crooke, Chairman, Founder and CEO, n-Lorem, about his long career and pioneering role in the antisense oligonucleotide (ASO) space, how RNA-targeting therapies are set to enter the mainstream, and his latest focus: making personalized, free-for-life ASO therapies available to nano-rare patient populations. ]]></itunes:summary>
    <description><![CDATA[<p><b>Roisin McGuigan</b>, Commissioning Editor, <em>Nucleic Acid Insights</em>, speaks to <b>Stanley Crooke</b>, Chairman, Founder and CEO, n-Lorem, about his long career and pioneering role in the antisense oligonucleotide (ASO) space, how RNA-targeting therapies are set to enter the mainstream, and his latest focus: making personalized, free-for-life ASO therapies available to nano-rare patient populations.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Roisin McGuigan</b>, Commissioning Editor, <em>Nucleic Acid Insights</em>, speaks to <b>Stanley Crooke</b>, Chairman, Founder and CEO, n-Lorem, about his long career and pioneering role in the antisense oligonucleotide (ASO) space, how RNA-targeting therapies are set to enter the mainstream, and his latest focus: making personalized, free-for-life ASO therapies available to nano-rare patient populations.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/16786295-for-the-many-and-the-few-bringing-aso-therapies-to-both-mainstream-and-nano-rare-indications.mp3" length="13829378" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-16786295</guid>
    <pubDate>Thu, 13 Mar 2025 16:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/16786295/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="For the many and the few: bringing ASO therapies to both mainstream and nano-rare indications" />
  <psc:chapter start="0:48" title="Could you tell me a bit about your career, from entering the oligonucleotide space to founding the n-Lorem Foundation?" />
  <psc:chapter start="2:34" title="How has the antisense field evolved over the time you&#39;ve been active in this space, and what would you pick out as the biggest milestones to date?" />
  <psc:chapter start="4:25" title="Could you tell me a bit more about the current key activities and goals of the foundation?" />
  <psc:chapter start="7:32" title="You have published some very positive clinical data recently. Can you discuss some of those key clinical milestones to date, and what&#39;s next?" />
  <psc:chapter start="12:04" title="Where are the key opportunities as you see them to improve targeted delivery of ASO therapies?" />
  <psc:chapter start="15:27" title="How do you predict the ASO space will develop over the next five years,  an what will be your own key priorities in that timeframe?" />
</psc:chapters>
    <itunes:duration>1149</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>4</itunes:season>
    <itunes:episode>2</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Exploring challenges, opportunities and state-of-the-art tools in the lipid nanoparticle space</itunes:title>
    <title>Exploring challenges, opportunities and state-of-the-art tools in the lipid nanoparticle space</title>
    <itunes:summary><![CDATA[Róisin McGuigan, Commissioning Editor, Nucleic Acid Insights, speaks to Ketaki Deshmukh, Senior Scientist, Novo Nordisk, about advanced characterization tools for LNPs, challenges in extrahepatic delivery, scalability issues, and the potential impact of AI and machine learning (ML) on future LNP development. ]]></itunes:summary>
    <description><![CDATA[<p><b>Róisin McGuigan</b>, Commissioning Editor, <em>Nucleic Acid Insights</em>, speaks to <b>Ketaki Deshmukh</b>, Senior Scientist, Novo Nordisk, about advanced characterization tools for LNPs, challenges in extrahepatic delivery, scalability issues, and the potential impact of AI and machine learning (ML) on future LNP development.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Róisin McGuigan</b>, Commissioning Editor, <em>Nucleic Acid Insights</em>, speaks to <b>Ketaki Deshmukh</b>, Senior Scientist, Novo Nordisk, about advanced characterization tools for LNPs, challenges in extrahepatic delivery, scalability issues, and the potential impact of AI and machine learning (ML) on future LNP development.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/16646047-exploring-challenges-opportunities-and-state-of-the-art-tools-in-the-lipid-nanoparticle-space.mp3" length="10877285" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-16646047</guid>
    <pubDate>Wed, 19 Feb 2025 09:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/16646047/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="What are you currently working on?" />
  <psc:chapter start="2:46" title="What are the key challenges for extrahepatic delivery using LNPs and the most promising avenues for achieving targeted delivery?" />
  <psc:chapter start="6:10" title="What would you identify as the current state-of-the-art in terms of advanced characterization tools available for LNPs?" />
  <psc:chapter start="9:41" title="What are the key current challenges in LNP process development?" />
  <psc:chapter start="10:47" title="What are the key parameters to consider when looking at successful scalability of LNPs?" />
  <psc:chapter start="12:00" title="When and how do you predict the industry will move forward in the LNP space and leverage nanoparticle delivery?" />
  <psc:chapter start="13:44" title="What are your own key goals and priorities for the next few years?" />
</psc:chapters>
    <itunes:duration>903</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>4</itunes:season>
    <itunes:episode>1</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Driving innovation in cell and gene therapy: the role of AI and robotics</itunes:title>
    <title>Driving innovation in cell and gene therapy: the role of AI and robotics</title>
    <itunes:summary><![CDATA[Jokūbas Leikauskas, Editor, Cell &amp; Gene Therapy Insights, speaks with OmniaBio Inc.’s Kenneth Harris, Chief Strategy Officer and Head of AI, Mitchel Sivilotti, President and CEO, and Anthony Rotunno, Senior Vice President and General Manager/Site Head, about the innovative advancements in cell and gene therapy, focusing on how AI, automation, and robotics are revolutionizing manufacturing processes by reducing costs, increasing production capacity, and ultimately, improving patient outcom...]]></itunes:summary>
    <description><![CDATA[<p><b>Jokūbas Leikauskas</b>, Editor, <em>Cell &amp; Gene Therapy Insights</em>, speaks with OmniaBio Inc.’s <b>Kenneth Harris</b>, Chief Strategy Officer and Head of AI, <b>Mitchel Sivilotti</b>, President and CEO, and <b>Anthony Rotunno</b>, Senior Vice President and General Manager/Site Head, about the innovative advancements in cell and gene therapy, focusing on how AI, automation, and robotics are revolutionizing manufacturing processes by reducing costs, increasing production capacity, and ultimately, improving patient outcomes in the rapidly evolving cell and gene therapy field. </p>]]></description>
    <content:encoded><![CDATA[<p><b>Jokūbas Leikauskas</b>, Editor, <em>Cell &amp; Gene Therapy Insights</em>, speaks with OmniaBio Inc.’s <b>Kenneth Harris</b>, Chief Strategy Officer and Head of AI, <b>Mitchel Sivilotti</b>, President and CEO, and <b>Anthony Rotunno</b>, Senior Vice President and General Manager/Site Head, about the innovative advancements in cell and gene therapy, focusing on how AI, automation, and robotics are revolutionizing manufacturing processes by reducing costs, increasing production capacity, and ultimately, improving patient outcomes in the rapidly evolving cell and gene therapy field. </p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/16509550-driving-innovation-in-cell-and-gene-therapy-the-role-of-ai-and-robotics.mp3" length="11429374" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-16509550</guid>
    <pubDate>Mon, 27 Jan 2025 12:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/16509550/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Driving innovation in cell and gene therapy: the role of AI and robotics" />
  <psc:chapter start="1:48" title="What makes CGT a pivotal advancement in the evolution of modern medicine, and how do you envision this field evolving in the coming years?" />
  <psc:chapter start="2:57" title="What is the main mission of OmniaBio?" />
  <psc:chapter start="5:30" title="What sets OmniaBio apart in the field of CGT manufacturing?" />
  <psc:chapter start="7:56" title="How are you implementing AI and robotics to improve CGT manufacturing?" />
  <psc:chapter start="10:46" title="What are the challenges and concerns regarding AI and how are you planning to address them?" />
  <psc:chapter start="12:50" title="What excites you the most about the future of OmniaBio in the context of the rapidly evolving CGT industry?" />
</psc:chapters>
    <itunes:duration>938</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>12</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Spatial mapping: shaping the future of I-O diagnostics  and treatment</itunes:title>
    <title>Spatial mapping: shaping the future of I-O diagnostics  and treatment</title>
    <itunes:summary><![CDATA[Lauren Coyle, Commissioning Editor, Immuno-Oncology Insights, speaks with Banafshé Larijani, Director of the Centre for Therapeutic Innovation, University of Bath, about the development and application of a novel spatial mapping technology designed to improve cancer diagnostics and personalize treatment planning. ]]></itunes:summary>
    <description><![CDATA[<p><b>Lauren Coyle</b>, Commissioning Editor, <em>Immuno-Oncology Insights</em>, speaks with <b>Banafshé Larijani</b>, Director of the Centre for Therapeutic Innovation, University of Bath, about the development and application of a novel spatial mapping technology designed to improve cancer diagnostics and personalize treatment planning.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Lauren Coyle</b>, Commissioning Editor, <em>Immuno-Oncology Insights</em>, speaks with <b>Banafshé Larijani</b>, Director of the Centre for Therapeutic Innovation, University of Bath, about the development and application of a novel spatial mapping technology designed to improve cancer diagnostics and personalize treatment planning.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/16232574-spatial-mapping-shaping-the-future-of-i-o-diagnostics-and-treatment.mp3" length="28185127" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-16232574</guid>
    <pubDate>Fri, 06 Dec 2024 15:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/16232574/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Spatial mapping: shaping the future of I-O diagnostics  and treatment" />
  <psc:chapter start="1:16" title="1.	Can you both tell me a bit about your career and what you are currently working on?" />
  <psc:chapter start="4:27" title="2.	How does spatial mapping improve the accuracy of cancer diagnosis and treatment planning for clinicians?" />
  <psc:chapter start="11:07" title="3.	In what ways has spatial mapping contributed to the personalization of cancer treatment, particularly in cases such as clear cell renal carcinoma?" />
  <psc:chapter start="21:34" title="4.	What are the benefits of using FuncOmap for patient stratification and treatment decision-making?" />
  <psc:chapter start="29:11" title="5.	How might the insights gained from the study be applied to other types of cancer and how do you envision its integration into routine clinical practice?" />
  <psc:chapter start="33:24" title="6.	What excites you most about the potential of spatial mapping, specifically FuncOmap, in the field of cancer treatment?" />
  <psc:chapter start="36:02" title="7.	Finally, what are the key future perspectives for the next five years?" />
</psc:chapters>
    <itunes:duration>2324</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>11</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Pioneering quality control in biomanufacturing of cell and gene therapies</itunes:title>
    <title>Pioneering quality control in biomanufacturing of cell and gene therapies</title>
    <itunes:summary><![CDATA[Lauren Coyle, Commissioning Editor, speaks with Dhruv Sareen, Executive Director at Cedars-Sinai Biomanufacturing Center, and Johnathan Rodriguez, Quality Control Manager at Cedars-Sinai Biomanufacturing Center, about the roles of in-process controls, method validation, risk management, and automation in biomanufacturing. They will highlight strategies to ensure product safety, consistency, and regulatory compliance for cell and gene therapy products. ]]></itunes:summary>
    <description><![CDATA[<p><b>Lauren Coyle</b>, Commissioning Editor, speaks with <b>Dhruv Sareen</b>, Executive Director at Cedars-Sinai Biomanufacturing Center, and <b>Johnathan Rodriguez</b>, Quality Control Manager at Cedars-Sinai Biomanufacturing Center, about the roles of in-process controls, method validation, risk management, and automation in biomanufacturing. They will highlight strategies to ensure product safety, consistency, and regulatory compliance for cell and gene therapy products.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Lauren Coyle</b>, Commissioning Editor, speaks with <b>Dhruv Sareen</b>, Executive Director at Cedars-Sinai Biomanufacturing Center, and <b>Johnathan Rodriguez</b>, Quality Control Manager at Cedars-Sinai Biomanufacturing Center, about the roles of in-process controls, method validation, risk management, and automation in biomanufacturing. They will highlight strategies to ensure product safety, consistency, and regulatory compliance for cell and gene therapy products.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/16227852-pioneering-quality-control-in-biomanufacturing-of-cell-and-gene-therapies.mp3" length="20303813" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-16227852</guid>
    <pubDate>Thu, 05 Dec 2024 17:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/16227852/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Pioneering quality control in biomanufacturing of cell and gene therapies" />
  <psc:chapter start="1:27" title="1.	Can you tell us a bit briefly about your background and what you are currently working on?" />
  <psc:chapter start="4:38" title="2.	How do you establish in-process controls and release specifications for specific intermediate cell banks, drug substances, and final drug products?" />
  <psc:chapter start="10:24" title="3.	Looking at in-process QC testing, why is this important for the development of cell banks such as iPSCs and final cell therapy products?" />
  <psc:chapter start="13:31" title="4.	Can you explain the distinction between method qualification and method validation in the context of cell-based therapies and how does each contribute to ensuring product safety and efficacy?" />
  <psc:chapter start="17:43" title="5.	What role does risk management play in the overall QC strategy for cell-based therapies and how are these integrated into the decision-making process?" />
  <psc:chapter start="24:39" title="6.	Do you currently employ or plan to implement automated QC testing methods in your processes. If so, what advantages do you anticipate that these methods will bring to your QC strategy?" />
</psc:chapters>
    <itunes:duration>1688</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>10</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Preparing for tomorrow’s cell and gene therapies today: lessons from 30 years in the field</itunes:title>
    <title>Preparing for tomorrow’s cell and gene therapies today: lessons from 30 years in the field</title>
    <itunes:summary><![CDATA[For the first time in history, cell and gene therapy products are reaching the market in waves rather than in one’s and two’s, creating unprecedented challenges for pharma/biotech and healthcare sector stakeholders alike. David McCall, Senior Editor, BioInsights, speaks to Eric Faulkner, President and Chief Strategist, Passage Health Associates, about the chequered history of market access in the advanced therapies field, and what lessons can be taken forward to ensure a successful and sustai...]]></itunes:summary>
    <description><![CDATA[<p>For the first time in history, cell and gene therapy products are reaching the market in waves rather than in one’s and two’s, creating unprecedented challenges for pharma/biotech and healthcare sector stakeholders alike. <b>David McCall</b>, Senior Editor, BioInsights, speaks to <b>Eric Faulkner</b>, President and Chief Strategist, Passage Health Associates, about the chequered history of market access in the advanced therapies field, and what lessons can be taken forward to ensure a successful and sustainable commercial future for the sector. </p>]]></description>
    <content:encoded><![CDATA[<p>For the first time in history, cell and gene therapy products are reaching the market in waves rather than in one’s and two’s, creating unprecedented challenges for pharma/biotech and healthcare sector stakeholders alike. <b>David McCall</b>, Senior Editor, BioInsights, speaks to <b>Eric Faulkner</b>, President and Chief Strategist, Passage Health Associates, about the chequered history of market access in the advanced therapies field, and what lessons can be taken forward to ensure a successful and sustainable commercial future for the sector. </p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/15568412-preparing-for-tomorrow-s-cell-and-gene-therapies-today-lessons-from-30-years-in-the-field.mp3" length="18472884" type="audio/mpeg" />
    <itunes:author></itunes:author>
    <guid isPermaLink="false">Buzzsprout-15568412</guid>
    <pubDate>Fri, 06 Sep 2024 10:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/15568412/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Preparing for tomorrow’s cell and gene therapies today: lessons from 30 years in the field" />
  <psc:chapter start="1:15" title="What are the greatest challenges in the CGT space today versus 30 years ago? " />
  <psc:chapter start="7:44" title="And what are the greatest opportunities in CGT market access today?" />
  <psc:chapter start="10:53" title="What are some of the things that helped make the launch of Zolgensma so successful?" />
  <psc:chapter start="16:15" title="How does the increasing number of CGT product launches change the market access dynamic? " />
  <psc:chapter start="21:33" title="What do commercial mRNA and gene editing products mean for the CGT space?" />
  <psc:chapter start="23:50" title="What is your key recommendation to CGT developers for commercialization success?" />
</psc:chapters>
    <itunes:duration>1536</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>9</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Insights into advanced therapies in the context of evolving funding and M&amp;A environments</itunes:title>
    <title>Insights into advanced therapies in the context of evolving funding and M&amp;A environments</title>
    <itunes:summary><![CDATA[David McCall, Senior Editor, BioInsights, spoke to Lee Brown, Healthcare Sector Global Team Leader, Third Bridge Group, on Tuesday, February 6, 2024 to gain his insights into the fast-moving market landscape of advanced therapies. The discussion outlines key recent news and strategic moves from prominent pharma and biotech companies in the field, as well as the prospects for specific technologies such as CRISPR-based genome editing and next-generation CAR-T therapies. ]]></itunes:summary>
    <description><![CDATA[<p><b>David McCall</b>, Senior Editor, BioInsights, spoke to <b>Lee Brown</b>, Healthcare Sector Global Team Leader, Third Bridge Group, on Tuesday, February 6, 2024 to gain his insights into the fast-moving market landscape of advanced therapies. The discussion outlines key recent news and strategic moves from prominent pharma and biotech companies in the field, as well as the prospects for specific technologies such as CRISPR-based genome editing and next-generation CAR-T therapies.</p>]]></description>
    <content:encoded><![CDATA[<p><b>David McCall</b>, Senior Editor, BioInsights, spoke to <b>Lee Brown</b>, Healthcare Sector Global Team Leader, Third Bridge Group, on Tuesday, February 6, 2024 to gain his insights into the fast-moving market landscape of advanced therapies. The discussion outlines key recent news and strategic moves from prominent pharma and biotech companies in the field, as well as the prospects for specific technologies such as CRISPR-based genome editing and next-generation CAR-T therapies.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/15250976-insights-into-advanced-therapies-in-the-context-of-evolving-funding-and-m-a-environments.mp3" length="16328345" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-15250976</guid>
    <pubDate>Fri, 14 Jun 2024 16:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/15250976/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Insights into advanced therapies in the context of evolving funding and M&amp;A environments" />
  <psc:chapter start="2:01" title="Key recent deals and funding stories in CGT biotech: Karuna Therapeutics, Cerevel Therapeutics, Gracell Biotech, CG Oncology, Kyverna Therapeutics" />
  <psc:chapter start="7:27" title="Key recent deals and funding stories in CGT biotech: Metagenomi " />
  <psc:chapter start="8:47" title="Key recent deals and funding stories in CGT biotech: Tome Biosciences." />
  <psc:chapter start="10:14" title="Key recent deals and funding stories in CGT biotech: Beam Therapeutics, Caribou Biosciences" />
  <psc:chapter start="13:13" title="The story of Casgevy’s approval" />
  <psc:chapter start="15:30" title="The story of Roctavian’s approval" />
  <psc:chapter start="16:55" title="Sarepta Therapeutics" />
  <psc:chapter start="18:20" title="How do you view the CAR-T cell therapy space, both currently and moving forward?" />
  <psc:chapter start="20:09" title="Any other highlights from JP Morgan week 2024?" />
</psc:chapters>
    <itunes:duration>1357</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>8</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Fit for function: developing potency assays reflective of the in vivo environment</itunes:title>
    <title>Fit for function: developing potency assays reflective of the in vivo environment</title>
    <itunes:summary><![CDATA[Translating the therapeutic promise of cell and gene therapies into clinical reality relies on robust potency assays. However, designing assays that accurately reflect the complex mechanisms of these therapies can feel like chasing a moving target. Here, Charlotte Barker, Editor, Cell &amp; Gene Therapy Insights, speaks with Giorgio Zenere, CMC technical project lead in the Global QC Technology Innovation Team, Kite Pharma, and Dirk Windgassen, Director of Analytical Development, Miltenyi Bio...]]></itunes:summary>
    <description><![CDATA[<p>Translating the therapeutic promise of cell and gene therapies into clinical reality relies on robust potency assays. However, designing assays that accurately reflect the complex mechanisms of these therapies can feel like chasing a moving target. Here, <b>Charlotte Barker</b>, Editor, <em>Cell &amp; Gene Therapy Insights</em>, speaks with <b>Giorgio Zenere</b>, CMC technical project lead in the Global QC Technology Innovation Team, Kite Pharma, and <b>Dirk Windgassen</b>, Director of Analytical Development, Miltenyi Biotec, to discuss best practices and future trends in developing potency assays for cell and gene therapies.</p>]]></description>
    <content:encoded><![CDATA[<p>Translating the therapeutic promise of cell and gene therapies into clinical reality relies on robust potency assays. However, designing assays that accurately reflect the complex mechanisms of these therapies can feel like chasing a moving target. Here, <b>Charlotte Barker</b>, Editor, <em>Cell &amp; Gene Therapy Insights</em>, speaks with <b>Giorgio Zenere</b>, CMC technical project lead in the Global QC Technology Innovation Team, Kite Pharma, and <b>Dirk Windgassen</b>, Director of Analytical Development, Miltenyi Biotec, to discuss best practices and future trends in developing potency assays for cell and gene therapies.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/15045638-fit-for-function-developing-potency-assays-reflective-of-the-in-vivo-environment.mp3" length="20484834" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-15045638</guid>
    <pubDate>Fri, 10 May 2024 14:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/15045638/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Fit for function: developing potency assays reflective of the in vivo environment" />
  <psc:chapter start="0:55" title="Can you each start by introducing yourselves and telling us about what you are working on right now?" />
  <psc:chapter start="2:45" title="What are the greatest challenges in developing potency assays for cell and gene therapies?" />
  <psc:chapter start="6:40" title="What is the latest regulatory guidance on potency assays for cell and gene therapy, and are there any areas of disharmony?" />
  <psc:chapter start="10:45" title="How can assay development be streamlined, while maintaining cost-effectiveness and safety?" />
  <psc:chapter start="14:11" title="What strategies can we use to address the variability inherent to cell and gene therapies?" />
  <psc:chapter start="19:15" title="What technological advances do you see coming down the line for CGT assay development?" />
  <psc:chapter start="23:28" title="What best practices would you recommend to cell and gene therapy developers in potency assay development?" />
</psc:chapters>
    <itunes:duration>1700</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>7</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Gene therapy is having a monumental year: how can the industry keep up with supply?</itunes:title>
    <title>Gene therapy is having a monumental year: how can the industry keep up with supply?</title>
    <itunes:summary><![CDATA[Lauren Coyle, Commissioning Editor, Cell &amp; Gene Therapy Insights, talks with Suman Subramanian, Head of Commercial Operations, Catalent Cell and Gene Therapy, to discuss the major achievements in the gene therapy market in 2023, with a focus on reliable manufacturing processes and strategies to enhance predictability while reducing waste in gene therapy manufacturing. ]]></itunes:summary>
    <description><![CDATA[<p><b>Lauren Coyle</b>, Commissioning Editor, <em>Cell &amp; Gene Therapy Insights</em>, talks with<b> Suman Subramanian</b>, Head of Commercial Operations, Catalent Cell and Gene Therapy, to discuss the major achievements in the gene therapy market in 2023, with a focus on reliable manufacturing processes and strategies to enhance predictability while reducing waste in gene therapy manufacturing.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Lauren Coyle</b>, Commissioning Editor, <em>Cell &amp; Gene Therapy Insights</em>, talks with<b> Suman Subramanian</b>, Head of Commercial Operations, Catalent Cell and Gene Therapy, to discuss the major achievements in the gene therapy market in 2023, with a focus on reliable manufacturing processes and strategies to enhance predictability while reducing waste in gene therapy manufacturing.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/14827756-gene-therapy-is-having-a-monumental-year-how-can-the-industry-keep-up-with-supply.mp3" length="17035700" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-14827756</guid>
    <pubDate>Thu, 04 Apr 2024 14:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/14827756/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Gene therapy is having a monumental year: how can the industry keep up with supply?" />
  <psc:chapter start="0:56" title="Lets start with the key milestones achieved in the gene therapy market in 2023 and how these advancements have impacted the therapeutic landscape." />
  <psc:chapter start="2:12" title="What supply chain strategies have proven effective in addressing accelerated timelines associated with gene therapy development?" />
  <psc:chapter start="4:33" title="Focusing on the challenges in developing reliable and scalable manufacturing process for gene therapies, what strategies or innovation can be implemented to overcome these to ensure a robust manufacturing pipeline?" />
  <psc:chapter start="7:13" title="Can you elaborate on the specific challenges in AAV development and manufacturing and how the industry is working to overcome them?" />
  <psc:chapter start="8:59" title="How can companies effectively plan early for a commercial-ready process, and what role does collaboration with experienced partners play in achieving this goal?" />
  <psc:chapter start="11:21" title="How can a partner with late-phase and commercial manufacturing experience contribute to the success of gene therapy development, both in terms of solidifying processes and navigating the regulatory pathway?" />
  <psc:chapter start="13:09" title="Given the importance of supply chain management in delivering gene therapies to clinical trial locations, what specific needs and challenges should be considered, and how can they be effectively addressed?" />
  <psc:chapter start="15:15" title="How is the space evolving in terms of the ability to leverage platforms – for instance, in the area of platform assay development – and what are some keys to capitalizing on the benefits this offers?" />
  <psc:chapter start="17:19" title="‘Right first time’ is a key aspect of the Catalent approach – can you pick out some specific areas where this is particularly important?" />
  <psc:chapter start="19:34" title="Can you discuss some examples of successful simplification strategies in gene therapy manufacturing, and how they have positively impacted efficiency and reliability?" />
</psc:chapters>
    <itunes:duration>1416</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>6</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>A deep dive in to generative AI applications in I-O</itunes:title>
    <title>A deep dive in to generative AI applications in I-O</title>
    <itunes:summary><![CDATA[Lauren Coyle, Commissioning Editor, Immuno-Oncology Insights, speaks with André Freitas, Senior Lecturer (University of Manchester) and Research Group Leader (Idiap Research Institute/National Biomarker Centre), about the intersection of generative AI and experimental cancer treatments, with a focus on clinical trials, regulatory considerations, and leveraging emerging technologies for a transformative impact in I-O.    ]]></itunes:summary>
    <description><![CDATA[<p><b>Lauren Coyle</b>, Commissioning Editor, <em>Immuno-Oncology Insights</em>, speaks with <b>André Freitas</b>, Senior Lecturer (University of Manchester) and Research Group Leader (Idiap Research Institute/National Biomarker Centre), about the intersection of generative AI and experimental cancer treatments, with a focus on clinical trials, regulatory considerations, and leveraging emerging technologies for a transformative impact in I-O. <br/><br/></p>]]></description>
    <content:encoded><![CDATA[<p><b>Lauren Coyle</b>, Commissioning Editor, <em>Immuno-Oncology Insights</em>, speaks with <b>André Freitas</b>, Senior Lecturer (University of Manchester) and Research Group Leader (Idiap Research Institute/National Biomarker Centre), about the intersection of generative AI and experimental cancer treatments, with a focus on clinical trials, regulatory considerations, and leveraging emerging technologies for a transformative impact in I-O. <br/><br/></p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/14709839-a-deep-dive-in-to-generative-ai-applications-in-i-o.mp3" length="31621510" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-14709839</guid>
    <pubDate>Mon, 18 Mar 2024 10:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/14709839/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="A deep dive in to generative AI applications in I-O" />
  <psc:chapter start="1:12" title="Can you tell us briefly about your background in generative AI?" />
  <psc:chapter start="2:02" title="Can you explain the concept of generative AI and how this differs from other types of machine learning?" />
  <psc:chapter start="8:25" title="How can generative AI be employed to enhance the analysis of diverse data sets, specifically in the I-O space?" />
  <psc:chapter start="16:58" title="What are other potential applications of generative AI in the context of experimental cancer medicine?" />
  <psc:chapter start="24:33" title="Further to that, can you discuss the role of generative AI in optimizing and personalizing treatment strategies for cancer patients participating in clinical trials?" />
  <psc:chapter start="26:32" title="What considerations should be taken when developing generative AI models in the context of I-O?" />
  <psc:chapter start="32:15" title="Following this, what challenges have arisen so far, and how should these be addressed moving forward?" />
  <psc:chapter start="34:44" title="What regulatory challenges and considerations should be considered when implementing generative AI?" />
  <psc:chapter start="38:28" title="Lastly, what do you see as the future trends and advancements in generative AI for supporting experimental cancer medicine? What emerging technologies could contribute to this?" />
</psc:chapters>
    <itunes:duration>2632</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>5</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Developing novel radioimmunotherapy combinations for lung cancer treatment</itunes:title>
    <title>Developing novel radioimmunotherapy combinations for lung cancer treatment</title>
    <itunes:summary><![CDATA[Lauren Coyle, Commissioning Editor, Immuno-Oncology Insights, speaks to Joe Chang, Clinical Thoracic Oncologist, MD Anderson Cancer Center, University of Texas, who discusses his team’s pioneering work in combining radiation therapy with immunotherapy for lung cancer treatment. He highlights the challenges and promises of optimizing radioimmunotherapy combinations, emphasizing the importance of personalized treatment approaches and collaboration across disciplines to improve patient outcomes. ]]></itunes:summary>
    <description><![CDATA[<p><b>Lauren Coyle</b>, Commissioning Editor,<em> Immuno-Oncology Insights</em>, speaks to <b>Joe Chang</b>, Clinical Thoracic Oncologist, MD Anderson Cancer Center, University of Texas, who discusses his team’s pioneering work in combining radiation therapy with immunotherapy for lung cancer treatment. He highlights the challenges and promises of optimizing radioimmunotherapy combinations, emphasizing the importance of personalized treatment approaches and collaboration across disciplines to improve patient outcomes.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Lauren Coyle</b>, Commissioning Editor,<em> Immuno-Oncology Insights</em>, speaks to <b>Joe Chang</b>, Clinical Thoracic Oncologist, MD Anderson Cancer Center, University of Texas, who discusses his team’s pioneering work in combining radiation therapy with immunotherapy for lung cancer treatment. He highlights the challenges and promises of optimizing radioimmunotherapy combinations, emphasizing the importance of personalized treatment approaches and collaboration across disciplines to improve patient outcomes.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/14676120-developing-novel-radioimmunotherapy-combinations-for-lung-cancer-treatment.mp3" length="10806164" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-14676120</guid>
    <pubDate>Tue, 12 Mar 2024 14:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/14676120/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Developing novel radioimmunotherapy combinations for lung cancer treatment" />
  <psc:chapter start="1:11" title="Can you provide a brief overview of your background and experience in the field of combination radioimmunotherapy, and what sparked your interest in this area?" />
  <psc:chapter start="2:57" title="How do you approach the selection of specific radioimmunotherapy combinations, and what factors do you consider in designing these protocols?" />
  <psc:chapter start="4:37" title="What are the current challenges associated with radioimmunotherapy, considering potential synergies and conflicts between these treatment modalities, and what promises are there to overcome these?" />
  <psc:chapter start="6:20" title="Can you share insights into how combination therapies have impacted patient outcomes in your research?" />
  <psc:chapter start="7:57" title="Collaboration is often essential in research. How do you collaborate with other professionals to enhance the effectiveness of combination therapies?" />
  <psc:chapter start="9:46" title="How do you stay updated on the latest advancements in the field and integrate these into your research?" />
  <psc:chapter start="11:34" title="What are the key goals and priorities for your work in the upcoming years?" />
  <psc:chapter start="13:01" title="Lastly, what is one piece of wisdom you would like to share with the field at large?" />
</psc:chapters>
    <itunes:duration>897</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>4</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Focusing on the fundamentals: what do and don’t we know about mRNA delivery?</itunes:title>
    <title>Focusing on the fundamentals: what do and don’t we know about mRNA delivery?</title>
    <itunes:summary><![CDATA[As excitement around the evolving field of mRNA continues to grow, there remain some fundamental questions to be answered. David McCall, Senior Editor, Nucleic Acid Insights, spoke with Monash University’s Colin Pouton, Professor of Pharmaceutical Biology and Angus Johnston, Associate Professor, ARC Future Fellow about the key limitations and unknowns of current mRNA delivery approaches, and critical areas for further research and innovation to propel the field forward. ]]></itunes:summary>
    <description><![CDATA[<p>As excitement around the evolving field of mRNA continues to grow, there remain some<br/>fundamental questions to be answered.<b> David McCall</b>, Senior Editor, <em>Nucleic Acid Insights</em>, spoke with Monash University’s <b>Colin Pouton</b>, Professor of Pharmaceutical Biology and <b>Angus Johnston</b>, Associate Professor, ARC Future Fellow about the key limitations and unknowns of current mRNA delivery approaches, and critical areas for further research and innovation to propel the field forward.</p>]]></description>
    <content:encoded><![CDATA[<p>As excitement around the evolving field of mRNA continues to grow, there remain some<br/>fundamental questions to be answered.<b> David McCall</b>, Senior Editor, <em>Nucleic Acid Insights</em>, spoke with Monash University’s <b>Colin Pouton</b>, Professor of Pharmaceutical Biology and <b>Angus Johnston</b>, Associate Professor, ARC Future Fellow about the key limitations and unknowns of current mRNA delivery approaches, and critical areas for further research and innovation to propel the field forward.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/14667126-focusing-on-the-fundamentals-what-do-and-don-t-we-know-about-mrna-delivery.mp3" length="32726526" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-14667126</guid>
    <pubDate>Mon, 11 Mar 2024 12:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/14667126/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Focusing on the fundamentals: what do and don’t we know about mRNA delivery?" />
  <psc:chapter start="0:25" title=" Introduction" />
  <psc:chapter start="3:27" title="Tell us about your background and current work in the nucleic acid delivery space" />
  <psc:chapter start="6:38" title="What for you is the current state of the art in terms of what we can do with mRNA?" />
  <psc:chapter start="10:07" title="What are the key limitations in extending the reach of mRNA technology?" />
  <psc:chapter start="13:53" title="What can and can&#39;t we target with mRNA?" />
  <psc:chapter start="18:28" title="What analytical tools and methods do you utilize?" />
  <psc:chapter start="24:20" title="What are some key learnings in terms of monitoring mRNA biodistribution and activity in vivo, and how can these be harnessed?" />
  <psc:chapter start="28:54" title="What do recent findings regarding mRNA delivery tell us about future R&amp;D priorities?" />
  <psc:chapter start="33:56" title="What will be some key areas for future innovation in the mRNA delivery space?" />
  <psc:chapter start="40:01" title="Summing up future goals and priorities" />
</psc:chapters>
    <itunes:duration>2724</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>3</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Navigating genomics and transcriptomics in the immuno-oncology space</itunes:title>
    <title>Navigating genomics and transcriptomics in the immuno-oncology space</title>
    <itunes:summary><![CDATA[Lauren Coyle, Commissioning Editor, Immuno-Oncology Insights, interviews Katie Campbell, Postdoctoral Fellow, Cancer Research Institute, about her current research on genomics, transcriptomics, and spatial profiling to address challenges in the I-O field. ]]></itunes:summary>
    <description><![CDATA[<p>Lauren Coyle, Commissioning Editor, Immuno-Oncology Insights, interviews Katie Campbell, Postdoctoral Fellow, Cancer Research Institute, about her current research on genomics, transcriptomics, and spatial profiling to address challenges in the I-O field.</p>]]></description>
    <content:encoded><![CDATA[<p>Lauren Coyle, Commissioning Editor, Immuno-Oncology Insights, interviews Katie Campbell, Postdoctoral Fellow, Cancer Research Institute, about her current research on genomics, transcriptomics, and spatial profiling to address challenges in the I-O field.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/14607339-navigating-genomics-and-transcriptomics-in-the-immuno-oncology-space.mp3" length="14724034" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-14607339</guid>
    <pubDate>Fri, 01 Mar 2024 12:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/14607339/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Navigating genomics and transcriptomics in the immuno-oncology space" />
  <psc:chapter start="0:59" title="Can you tell us a bit about your career in the I-O space so far and what you&#39;re currently working on? " />
  <psc:chapter start="2:33" title="Looking at genomics and transcriptomics data, how has this successfully been implemented in I-O so far and what challenges remain to be solved? " />
  <psc:chapter start="4:54" title="How can these challenges be addressed going forward? " />
  <psc:chapter start="6:01" title="How does the integration of spatial profiling data contribute to a better understanding of molecular drivers and cellular interactions? " />
  <psc:chapter start="10:03" title="When it comes to navigating these questions, do you think it is better to start with a clear hypothesis or are there different routes that work better?" />
  <psc:chapter start="12:03" title="In your current research on somatic alterations and antigen-presenting machinery, how do you approach the analysis of HLA genes? " />
  <psc:chapter start="14:03" title="Following that, what strategies have you employed to identify and characterize copy number alterations in the antigen-presenting machinery? " />
  <psc:chapter start="15:11" title="How do you collaborate with experts from different fields, and how has this contributed to the progress of your research? " />
  <psc:chapter start="17:54" title="Finally, what are your main goals and aspirations for the future? " />
</psc:chapters>
    <itunes:duration>1223</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>2</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Avian influenza and the risk of pandemic</itunes:title>
    <title>Avian influenza and the risk of pandemic</title>
    <itunes:summary><![CDATA[With the potential for avian influenza to transmit and spread amongst humans, an effective vaccine to increase pandemic preparedness is a global priority. Charlotte Barker, Editor, Vaccine Insights, speaks with Mathilde Richard, Principal Investigator &amp; Associate Professor at Erasmus MC, about investigating antigenic evolution of avian influenza viruses, developing better vaccines, and the need for proactive measures to ensure global preparedness in the face of evolving influenza threats. ]]></itunes:summary>
    <description><![CDATA[<p>With the potential for avian influenza to transmit and spread amongst humans, an effective vaccine to increase pandemic preparedness is a global priority. Charlotte Barker, Editor, Vaccine Insights, speaks with Mathilde Richard, Principal Investigator &amp; Associate Professor at Erasmus MC, about investigating antigenic evolution of avian influenza viruses, developing better vaccines, and the need for proactive measures to ensure global preparedness in the face of evolving influenza threats.</p>]]></description>
    <content:encoded><![CDATA[<p>With the potential for avian influenza to transmit and spread amongst humans, an effective vaccine to increase pandemic preparedness is a global priority. Charlotte Barker, Editor, Vaccine Insights, speaks with Mathilde Richard, Principal Investigator &amp; Associate Professor at Erasmus MC, about investigating antigenic evolution of avian influenza viruses, developing better vaccines, and the need for proactive measures to ensure global preparedness in the face of evolving influenza threats.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/14587305-avian-influenza-and-the-risk-of-pandemic.mp3" length="17062523" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-14587305</guid>
    <pubDate>Tue, 27 Feb 2024 17:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/14587305/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Avian influenza and the risk of pandemic" />
  <psc:chapter start="1:00" title="How did you get involved in the field of virology and, specifically, avian influenzas? " />
  <psc:chapter start="4:05" title="What HPAI subtypes are most concerning for human health?" />
  <psc:chapter start="8:20" title="What projects are you and your team working on right now? " />
  <psc:chapter start="12:16" title="How can your work be applied to develop more effective vaccines? " />
  <psc:chapter start="15:15" title="Where do you hope to be with your research in 5 years?" />
  <psc:chapter start="18:15" title="Are we doing enough to prevent or prepare for a possible influenza pandemic?" />
</psc:chapters>
    <itunes:duration>1418</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>3</itunes:season>
    <itunes:episode>1</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Exploring the landscape of novel targets &amp; pathways in immuno-oncology</itunes:title>
    <title>Exploring the landscape of novel targets &amp; pathways in immuno-oncology</title>
    <itunes:summary><![CDATA[Lauren Coyle, Editor, Immuno-Oncology Insights, speaks to Yvonne McGrath, Chief Scientific Officer, iTeos Therapeutics, about the current and emerging novel targets and pathways for the use of cancer therapy in the I-O field with a focus on small molecules and antibody targets. ]]></itunes:summary>
    <description><![CDATA[<p><b>Lauren Coyle, </b>Editor, <em>Immuno-Oncology Insights</em>, speaks to <b>Yvonne McGrath,</b> Chief Scientific Officer, iTeos Therapeutics, about the current and emerging novel targets and pathways for the use of cancer therapy in the I-O field with a focus on small molecules and antibody targets.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Lauren Coyle, </b>Editor, <em>Immuno-Oncology Insights</em>, speaks to <b>Yvonne McGrath,</b> Chief Scientific Officer, iTeos Therapeutics, about the current and emerging novel targets and pathways for the use of cancer therapy in the I-O field with a focus on small molecules and antibody targets.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/14083843-exploring-the-landscape-of-novel-targets-pathways-in-immuno-oncology.mp3" length="12340355" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-14083843</guid>
    <pubDate>Mon, 04 Dec 2023 12:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/14083843/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Exploring the landscape of novel targets &amp; pathways in immuno-oncology" />
  <psc:chapter start="1:01" title="Could you briefly describe your past experiences in cancer research and your current role at iTeos Therapeutics? " />
  <psc:chapter start="2:32" title="Could you give background on the novel targets and pathways development platform at iTeos? How do these represent an advance on previous work? " />
  <psc:chapter start="5:27" title="Can you tell me more about the research and development pipeline that this work fuels? " />
  <psc:chapter start="7:57" title="There&#39;s been an increased interest surrounding personalized medicine, do you think this will help with the development of personalized medicine?" />
  <psc:chapter start="8:57" title="What impact is being made by small-molecule targets and do you see any specific areas that require more focus?" />
  <psc:chapter start="10:18" title="Is there any progress in antibody targets, and how can they be further developed?" />
  <psc:chapter start="12:20" title="What challenges are currently facing the I-O field in terms of targeted therapies and how could these be addressed?" />
  <psc:chapter start="14:35" title="Finally, what are some key goals and priorities for your role and iTeos as a whole in the future?" />
</psc:chapters>
    <itunes:duration>1025</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>16</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Multiomics integration: advancing pediatric cancer immunotherapy</itunes:title>
    <title>Multiomics integration: advancing pediatric cancer immunotherapy</title>
    <itunes:summary><![CDATA[Lauren Coyle, Editor, Immuno-Oncology Insights, speaks with Raoul Santiago, Clinical Investigator and Associate Professor of Pediatric Hematology and Oncology, University Hospital Center, Laval University, to discuss the role of multiomics in the I-O setting and how these tools can be leveraged to improve pediatric cancer care. ]]></itunes:summary>
    <description><![CDATA[<p><b>Lauren Coyle</b>, Editor, Immuno-Oncology Insights, speaks with <b>Raoul Santiago</b>, Clinical Investigator and Associate Professor of Pediatric Hematology and Oncology, University Hospital Center, Laval University, to discuss the role of multiomics in the I-O setting and how these tools can be leveraged to improve pediatric cancer care.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Lauren Coyle</b>, Editor, Immuno-Oncology Insights, speaks with <b>Raoul Santiago</b>, Clinical Investigator and Associate Professor of Pediatric Hematology and Oncology, University Hospital Center, Laval University, to discuss the role of multiomics in the I-O setting and how these tools can be leveraged to improve pediatric cancer care.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/13894780-multiomics-integration-advancing-pediatric-cancer-immunotherapy.mp3" length="14164908" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-13894780</guid>
    <pubDate>Thu, 02 Nov 2023 12:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/13894780/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Multiomics integration: advancing pediatric cancer immunotherapy" />
  <psc:chapter start="1:02" title="Can you tell us a bit about your current role and the work that you do?" />
  <psc:chapter start="1:52" title="Could you tell us more about how you apply these multiomic approaches in your work and what the cutting edge in the area is for you?" />
  <psc:chapter start="4:44" title="What impact are these tools having on our understanding of the immune response/immunotherapy approaches to cancer? " />
  <psc:chapter start="9:42" title="What progress do you see being made in the ongoing search for novel biomarkers in the I-O space, and what will be the keys to their successful deployment? " />
  <psc:chapter start="11:40" title="What should be the next specific targets for the oncology field in terms of further improving our knowledge of the underlying biology of the immune response/tumor microenvironment? What tools will be key in achieving success in these efforts?" />
  <psc:chapter start="13:04" title="What would be top of your wish list for new innovations in this space?" />
  <psc:chapter start="15:57" title="What will be your own key goals and priorities in the next few years? " />
</psc:chapters>
    <itunes:duration>1177</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>15</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Building with the patient in mind: designing a state-of-the-art facility for viral vector manufacturing</itunes:title>
    <title>Building with the patient in mind: designing a state-of-the-art facility for viral vector manufacturing</title>
    <itunes:summary><![CDATA[The cell and gene therapy space poses a number of unique challenges when it comes to facility design. In this episode, Róisin McGuigan, Editor, BioInsights, speaks to Yposkesi’s Louis-Marie De Montgrand and Morad El Gueddari to discuss the key considerations for designing an advanced therapy manufacturing facility that can meet the needs of future commercial demand.  To read this interview and access lots more content, visit the Cell and Gene Therapy Insights website. ]]></itunes:summary>
    <description><![CDATA[<p>The cell and gene therapy space poses a number of unique challenges when it comes to facility design. In this episode, <b>Róisin McGuigan</b>, Editor, BioInsights, speaks to Yposkesi’s<b> Louis-Marie De Montgrand </b>and <b>Morad El Gueddari </b>to discuss the key considerations for designing an advanced therapy manufacturing facility that can meet the needs of future commercial demand.<br/><br/>To read this interview and access lots more content, visit the <em>Cell and Gene Therapy Insights</em> website.</p>]]></description>
    <content:encoded><![CDATA[<p>The cell and gene therapy space poses a number of unique challenges when it comes to facility design. In this episode, <b>Róisin McGuigan</b>, Editor, BioInsights, speaks to Yposkesi’s<b> Louis-Marie De Montgrand </b>and <b>Morad El Gueddari </b>to discuss the key considerations for designing an advanced therapy manufacturing facility that can meet the needs of future commercial demand.<br/><br/>To read this interview and access lots more content, visit the <em>Cell and Gene Therapy Insights</em> website.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/13749262-building-with-the-patient-in-mind-designing-a-state-of-the-art-facility-for-viral-vector-manufacturing.mp3" length="20726675" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-13749262</guid>
    <pubDate>Tue, 10 Oct 2023 10:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/13749262/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Building with the patient in mind: designing a state-of-the-art facility for viral vector manufacturing" />
  <psc:chapter start="1:54" title="Please introduce yourselves and tell us about the work you do" />
  <psc:chapter start="3:18" title="What are the unique challenges or needs when designing manufacturing facilities for CGT?" />
  <psc:chapter start="5:24" title="How did you apply your previous experience to designing a new facility?" />
  <psc:chapter start="11:26" title="How did you ensure the ability to meet future capacity requirements?" />
  <psc:chapter start="16:14" title="How are you ensuring a sufficient workforce to meet your needs?" />
  <psc:chapter start="23:05" title="What would be your key learnings and advice for successful CGT facility design?" />
  <psc:chapter start="26:47" title="What’s next for this project?" />
</psc:chapters>
    <itunes:duration>1724</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>14</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Can AAV continue to deliver the promise of gene therapy?</itunes:title>
    <title>Can AAV continue to deliver the promise of gene therapy?</title>
    <itunes:summary><![CDATA[In this episode, Charlotte Barker, Editor, BioInsights, will be discussing the future of AAV-based gene therapy manufacturing with Elie Hanania, VP of Process Development Viral Vector Technologies at Avid Bioservices, and Ratish Krishnan, Senior Strategy Consultant at Merck Life Sciences.  ]]></itunes:summary>
    <description><![CDATA[<p>In this episode, Charlotte Barker, Editor, BioInsights, will be discussing the future of AAV-based gene therapy manufacturing with Elie Hanania, VP of Process Development Viral Vector Technologies at Avid Bioservices, and Ratish Krishnan, Senior Strategy Consultant at Merck Life Sciences. </p>]]></description>
    <content:encoded><![CDATA[<p>In this episode, Charlotte Barker, Editor, BioInsights, will be discussing the future of AAV-based gene therapy manufacturing with Elie Hanania, VP of Process Development Viral Vector Technologies at Avid Bioservices, and Ratish Krishnan, Senior Strategy Consultant at Merck Life Sciences. </p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/13582860-can-aav-continue-to-deliver-the-promise-of-gene-therapy.mp3" length="15604166" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-13582860</guid>
    <pubDate>Wed, 13 Sep 2023 08:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/13582860/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Can AAV continue to deliver the promise of gene therapy?" />
  <psc:chapter start="0:50" title="Does AAV still reign supreme for advanced therapies? " />
  <psc:chapter start="5:50" title="What has AAV evolved over the past 5 years and how do you see the future?" />
  <psc:chapter start="11:54" title="As use of AAV continues to grow, what challenges stand in its way?" />
  <psc:chapter start="14:23" title="What promising innovations in AAV production do you see emerging over the next 5 years? " />
  <psc:chapter start="17:52" title="How can we streamline AAV manufacturing for common disease indications?" />
</psc:chapters>
    <itunes:duration>1297</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>13</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Expanding the potential of in vivo cell therapy with tLNP-RNAs (targeted lipid nanoparticle-RNA)</itunes:title>
    <title>Expanding the potential of in vivo cell therapy with tLNP-RNAs (targeted lipid nanoparticle-RNA)</title>
    <itunes:summary><![CDATA[The application of lipid nanoparticles (LNPs) as a non- viral delivery system for advanced therapies, in conjunction with RNA-based medicines, is set to revolutionize the field.  In this episode, David McCall, Senior Editor, BioInsights, speaks to Adrian Bot, Chief Scientific Officer and Executive Vice President of R&amp;D, Capstan Therapeutics, about the potential of these tools to drive the burgeoning in vivo cell therapy space in particular, and the broader gene medicine field in gene...]]></itunes:summary>
    <description><![CDATA[<p>The application of lipid nanoparticles (LNPs) as a non- viral delivery system for advanced therapies, in conjunction with RNA-based medicines, is set to revolutionize the field.  In this episode, David McCall, Senior Editor, BioInsights, speaks to Adrian Bot, Chief Scientific Officer and Executive Vice President of R&amp;D, Capstan Therapeutics, about the potential of these tools to drive the burgeoning <em>in vivo</em> cell therapy space in particular, and the broader gene medicine field in general.</p>]]></description>
    <content:encoded><![CDATA[<p>The application of lipid nanoparticles (LNPs) as a non- viral delivery system for advanced therapies, in conjunction with RNA-based medicines, is set to revolutionize the field.  In this episode, David McCall, Senior Editor, BioInsights, speaks to Adrian Bot, Chief Scientific Officer and Executive Vice President of R&amp;D, Capstan Therapeutics, about the potential of these tools to drive the burgeoning <em>in vivo</em> cell therapy space in particular, and the broader gene medicine field in general.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/13415002-expanding-the-potential-of-in-vivo-cell-therapy-with-tlnp-rnas-targeted-lipid-nanoparticle-rna.mp3" length="14485314" type="audio/mpeg" />
    <itunes:author>Adrian Bot</itunes:author>
    <guid isPermaLink="false">Buzzsprout-13415002</guid>
    <pubDate>Wed, 30 Aug 2023 09:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/13415002/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Expanding the potential of in vivo cell therapy with tLNP-RNAs (targeted lipid nanoparticle-RNA)" />
  <psc:chapter start="1:14" title="What have you have been working on lately?" />
  <psc:chapter start="1:37" title="What is the latest R&amp;D progress in the in vivo CAR-T cell therapy field?" />
  <psc:chapter start="3:10" title="Why is lipid nanoparticle technology ideal for in vivo CAR-T cell engineering?" />
  <psc:chapter start="5:37" title="Advantages of lipid nanoparticles over other gene delivery platforms" />
  <psc:chapter start="10:22" title="Exploring the cell targeting, systemic delivery potential, and broad applicability of LNPs" />
  <psc:chapter start="12:45" title="What LNP learnings from the mRNA field can be leveraged for CAR-T cell engineering?" />
  <psc:chapter start="15:25" title="What is the most surprising thing you have learned in your preclinical work to date?" />
  <psc:chapter start="15:50" title="What are you most excited about in terms of Capstan&#39;s future work?" />
  <psc:chapter start="17:03" title="What is Capstan&#39;s biggest challenge today and how are you addressing it?" />
  <psc:chapter start="17:59" title="What will be Capstan&#39;s biggest challenge in five years’ time? How to prepare for it?" />
</psc:chapters>
    <itunes:duration>1204</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>12</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Investing long-term in the cell &amp; gene therapies of the future</itunes:title>
    <title>Investing long-term in the cell &amp; gene therapies of the future</title>
    <itunes:summary><![CDATA[David McCall, Senior Editor, BioInsights, speaks to Geeta Vemuri, Founder and Managing Partner, Agent Capital, about her VC company's portfolio of advanced therapy investments, and the keys to obtaining funding in a difficult environment. (From an interview conducted on February 22nd, 2023). ]]></itunes:summary>
    <description><![CDATA[<p>David McCall, Senior Editor, BioInsights, speaks to Geeta Vemuri, Founder and Managing Partner, Agent Capital, about her VC company&apos;s portfolio of advanced therapy investments, and the keys to obtaining funding in a difficult environment. (From an interview conducted on February 22nd, 2023).</p>]]></description>
    <content:encoded><![CDATA[<p>David McCall, Senior Editor, BioInsights, speaks to Geeta Vemuri, Founder and Managing Partner, Agent Capital, about her VC company&apos;s portfolio of advanced therapy investments, and the keys to obtaining funding in a difficult environment. (From an interview conducted on February 22nd, 2023).</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/13408478-investing-long-term-in-the-cell-gene-therapies-of-the-future.mp3" length="11140787" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-13408478</guid>
    <pubDate>Tue, 22 Aug 2023 10:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/13408478/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Investing long-term in the cell &amp; gene therapies of the future" />
  <psc:chapter start="1:28" title="What have you been working on lately?" />
  <psc:chapter start="2:05" title="Agent Capital’s investment strategy and advanced therapies portfolio" />
  <psc:chapter start="5:29" title="What are the key areas of innovation for cell and gene therapy currently?" />
  <psc:chapter start="7:54" title="Current and future fundraising landscape for advanced therapy biotechs" />
  <psc:chapter start="11:30" title="Keys to attracting investment both now and in the future" />
  <psc:chapter start="13:01" title="Key future goals and priorities for Agent Capital and its portfolio companies" />
</psc:chapters>
    <itunes:duration>925</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>11</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Happy medium: considerations in scaling cell culture media strategies</itunes:title>
    <title>Happy medium: considerations in scaling cell culture media strategies</title>
    <itunes:summary><![CDATA[While attractive from an initial cost perspective, performing early development in a cell culture substrate that does not match a therapy’s final manufacturing platform can have critical implications on development timelines. In this podcast,  Charlotte Barker, Editor, BioInsights, speaks to Dalip Sethi, Director of Scientific Affairs, Terumo BCT, about best practices for scaling up cell culture substrate. ]]></itunes:summary>
    <description><![CDATA[<p>While attractive from an initial cost perspective, performing early development in a cell culture substrate that does not match a therapy’s final manufacturing platform can have critical implications on development timelines. In this podcast,  Charlotte Barker, Editor, BioInsights, speaks to Dalip Sethi, Director of Scientific Affairs, Terumo BCT, about best practices for scaling up cell culture substrate.</p>]]></description>
    <content:encoded><![CDATA[<p>While attractive from an initial cost perspective, performing early development in a cell culture substrate that does not match a therapy’s final manufacturing platform can have critical implications on development timelines. In this podcast,  Charlotte Barker, Editor, BioInsights, speaks to Dalip Sethi, Director of Scientific Affairs, Terumo BCT, about best practices for scaling up cell culture substrate.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/13414994-happy-medium-considerations-in-scaling-cell-culture-media-strategies.mp3" length="13856719" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-13414994</guid>
    <pubDate>Wed, 16 Aug 2023 09:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/13414994/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Happy medium: considerations in scaling cell culture media strategies" />
  <psc:chapter start="0:49" title="Cell culture media is a big consideration for therapy developers— does Terumo Blood and Cell Technologies (BCT) have a media offering?" />
  <psc:chapter start="1:58" title="What are some of the main considerations in choosing a cell culture medium?" />
  <psc:chapter start="7:59" title="What are the media-related considerations when you are using a closed automated bioreactor system—including the in-process analytical components?" />
  <psc:chapter start="10:57" title="Where do equipment and consumables factor into this conversation?" />
  <psc:chapter start="13:09" title="That’s very interesting to note… Not the ‘first line’ issues that you mentioned earlier, but certainly something that can affect therapy development timelines. What does Terumo BCT see as a mitigation strategy?" />
  <psc:chapter start="16:59" title="How would you say your customers’ needs are changing as the industry matures?" />
</psc:chapters>
    <itunes:duration>1151</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>10</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Applying multiomics to novel target discovery in immuno-oncology</itunes:title>
    <title>Applying multiomics to novel target discovery in immuno-oncology</title>
    <itunes:summary><![CDATA[In this episode, Róisin McGuigan, Editor, Immuno-Oncology Insights, speaks with Eran Ophir, Chief Scientific Officer, Compugen, and Yaron Turpaz, Senior Vice President and Senior Advisor, Data and Informatics Solutions, Compugen, about the advantages of using multiomic and computational approaches for the discovery of novel targets and mechanisms of action (MoA) of novel drug candidates in immuno-oncology.   ]]></itunes:summary>
    <description><![CDATA[<p>In this episode, Róisin McGuigan, Editor,<em> Immuno-Oncology Insights</em>, speaks with Eran Ophir, Chief Scientific Officer, Compugen, and Yaron Turpaz, Senior Vice President and Senior Advisor, Data and Informatics Solutions, Compugen, about the advantages of using multiomic and computational approaches for the discovery of novel targets and mechanisms of action (MoA) of novel drug candidates in immuno-oncology.<br/><br/></p>]]></description>
    <content:encoded><![CDATA[<p>In this episode, Róisin McGuigan, Editor,<em> Immuno-Oncology Insights</em>, speaks with Eran Ophir, Chief Scientific Officer, Compugen, and Yaron Turpaz, Senior Vice President and Senior Advisor, Data and Informatics Solutions, Compugen, about the advantages of using multiomic and computational approaches for the discovery of novel targets and mechanisms of action (MoA) of novel drug candidates in immuno-oncology.<br/><br/></p>]]></content:encoded>
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    <itunes:author>Eran Ophir and Yaron Turpaz</itunes:author>
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    <pubDate>Tue, 08 Aug 2023 10:00:00 +0000</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="Applying multiomics to novel target discovery in immuno-oncology" />
  <psc:chapter start="1:38" title="Can you both tell me a bit about your current roles and the work you do?" />
  <psc:chapter start="2:45" title="Can you outline how you are applying multiomics to novel target discovery in the I-O space?" />
  <psc:chapter start="4:25" title="What advantages do multiomics approaches offer, and what for you is the cutting edge in this space?" />
  <psc:chapter start="5:56" title="Can you tell me about Compugen’s computational approach to developing an I–O pipeline?" />
  <psc:chapter start="8:25" title="What have been your biggest milestones to date, and what’s next? " />
  <psc:chapter start="12:49" title="The development of diagnostic/prognostic biomarkers remains a key challenge for the I–O space–how can computational approaches help these efforts? " />
  <psc:chapter start="15:01" title="What would be top of your wish list for new tools/innovations in this space?" />
</psc:chapters>
    <itunes:duration>1122</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>9</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Modernizing cell therapy manufacturing to reduce vein-to-vein times</itunes:title>
    <title>Modernizing cell therapy manufacturing to reduce vein-to-vein times</title>
    <itunes:summary><![CDATA[Charlotte Barker (Editor, BioInsights) speaks with Curate Biosciences’ CEO David Backer and CTO Tony Ward about the need for CAR-T cell therapy manufacturing to evolve, and how a new cell separation technique could boost efficiency. ]]></itunes:summary>
    <description><![CDATA[<p>Charlotte Barker (Editor, BioInsights) speaks with Curate Biosciences’ CEO David Backer and CTO Tony Ward about the need for CAR-T cell therapy manufacturing to evolve, and how a new cell separation technique could boost efficiency.</p>]]></description>
    <content:encoded><![CDATA[<p>Charlotte Barker (Editor, BioInsights) speaks with Curate Biosciences’ CEO David Backer and CTO Tony Ward about the need for CAR-T cell therapy manufacturing to evolve, and how a new cell separation technique could boost efficiency.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/13293506-modernizing-cell-therapy-manufacturing-to-reduce-vein-to-vein-times.mp3" length="17245790" type="audio/mpeg" />
    <itunes:author>David Backer, CEO Curate Biosciences</itunes:author>
    <guid isPermaLink="false">Buzzsprout-13293506</guid>
    <pubDate>Wed, 26 Jul 2023 15:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/13293506/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Modernizing cell therapy manufacturing to reduce vein-to-vein times" />
  <psc:chapter start="0:49" title="How have you seen CAR-T cell therapies evolve over time?" />
  <psc:chapter start="3:00" title="What are the key challenges and priorities for CAR-T cell manufacture?" />
  <psc:chapter start="6:35" title="Why are the initial steps in apheresis or debulking important?" />
  <psc:chapter start="11:39" title="How does DCS microfluidics differ from other techniques?" />
  <psc:chapter start="14:37" title="How can DCS optimize the expansion of T cells?" />
  <psc:chapter start="16:56" title="Does cell separation impact subsequent genome editing steps?" />
  <psc:chapter start="21:12" title="Can manufacturing processes help ensure clinical efficacy?" />
</psc:chapters>
    <itunes:duration>1429</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>8</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Inducing innate immune responses with particulate adjuvants</itunes:title>
    <title>Inducing innate immune responses with particulate adjuvants</title>
    <itunes:summary><![CDATA[Charlotte Barker, Editor, Vaccine Insights, speaks with Ed Lavelle, Professor, Trinity College Dublin, about our growing understanding of adjuvant mechanisms, his work on developing mucosal vaccines, and why size matters for nanoparticles’ adjuvant effects. ]]></itunes:summary>
    <description><![CDATA[<p>Charlotte Barker, Editor, <em>Vaccine Insights</em>, speaks with Ed Lavelle, Professor, Trinity College Dublin, about our growing understanding of adjuvant mechanisms, his work on developing mucosal vaccines, and why size matters for nanoparticles’ adjuvant effects.</p>]]></description>
    <content:encoded><![CDATA[<p>Charlotte Barker, Editor, <em>Vaccine Insights</em>, speaks with Ed Lavelle, Professor, Trinity College Dublin, about our growing understanding of adjuvant mechanisms, his work on developing mucosal vaccines, and why size matters for nanoparticles’ adjuvant effects.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/13292182-inducing-innate-immune-responses-with-particulate-adjuvants.mp3" length="9858350" type="audio/mpeg" />
    <itunes:author>Ed Lavelle</itunes:author>
    <guid isPermaLink="false">Buzzsprout-13292182</guid>
    <pubDate>Wed, 26 Jul 2023 10:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/13292182/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Inducing innate immune responses with particulate adjuvants" />
  <psc:chapter start="0:50" title="How did you get involved in your current field of study?" />
  <psc:chapter start="2:30" title="What are the goals of your research? " />
  <psc:chapter start="3:57" title="What are the biggest gaps in our knowledge regarding adjuvants?" />
  <psc:chapter start="7:00" title="How is your research closing those gaps? " />
  <psc:chapter start="8:28" title="What are you working on right now? " />
  <psc:chapter start="9:25" title="Tell us more about your recent paper on nanoparticle size and adjuvanticity" />
  <psc:chapter start="12:23" title="What’s next for your work?" />
</psc:chapters>
    <itunes:duration>818</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>7</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Navigating the complexities of biodistribution, transgene expression &amp; vector shedding in gene therapy development</itunes:title>
    <title>Navigating the complexities of biodistribution, transgene expression &amp; vector shedding in gene therapy development</title>
    <itunes:summary><![CDATA[In this episode Róisin McGuigan (Editor, BioInsights) speaks to Paul Byrne (Senior Director, Genomics, ProtaGene) about the evolution of the gene therapy field, with a specific focus on the complexities posed by biodistribution, vector shedding, and transgene expression in gene therapy development. ]]></itunes:summary>
    <description><![CDATA[<p>In this episode Róisin McGuigan (Editor, BioInsights) speaks to Paul Byrne (Senior Director, Genomics, ProtaGene) about the evolution of the gene therapy field, with a specific focus on the complexities posed by biodistribution, vector shedding, and transgene expression in gene therapy development.</p>]]></description>
    <content:encoded><![CDATA[<p>In this episode Róisin McGuigan (Editor, BioInsights) speaks to Paul Byrne (Senior Director, Genomics, ProtaGene) about the evolution of the gene therapy field, with a specific focus on the complexities posed by biodistribution, vector shedding, and transgene expression in gene therapy development.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/13007099-navigating-the-complexities-of-biodistribution-transgene-expression-vector-shedding-in-gene-therapy-development.mp3" length="22434003" type="audio/mpeg" />
    <itunes:author>Paul Byrne</itunes:author>
    <guid isPermaLink="false">Buzzsprout-13007099</guid>
    <pubDate>Fri, 09 Jun 2023 07:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/13007099/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Navigating the complexities of biodistribution, transgene expression &amp; vector shedding in gene therapy development" />
  <psc:chapter start="1:17" title="You&#39;ve been working in gene therapy for a long time now. What do you see as the key learnings of the industry related to bioanalysis of in vivo therapeutic approaches? " />
  <psc:chapter start="6:24" title="What would you identify as the key commonalities – and the important differences – that exist in approaching bioanalysis of ex vivo gene-modified cell therapies? " />
  <psc:chapter start="9:25" title="How is the field of gene therapy evolving, and what new therapies and delivery methods do you see on the horizon? " />
  <psc:chapter start="13:43" title="Why are biodistribution, vector shedding, and transgene expression are such critical factors for ensuring the safety of cell and gene therapies?" />
  <psc:chapter start="15:27" title="Can you outline the key challenges associated with assessing and monitoring biodistribution and vector shedding?" />
  <psc:chapter start="20:13" title="What new approaches are being developed to address these challenges? And what impact is that introduction of digital PCR having? " />
  <psc:chapter start="27:18" title="How can the insights and best practices we&#39;ve discussed today be applied to specific R&amp;D efforts? What would your key advice be for our listeners who are working in this space? " />
</psc:chapters>
    <itunes:duration>1866</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>6</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Non-viral methods for ex vivo cell &amp; gene therapy: is the future non-viral?</itunes:title>
    <title>Non-viral methods for ex vivo cell &amp; gene therapy: is the future non-viral?</title>
    <itunes:summary><![CDATA[Non-viral methods for ex vivo cell &amp; gene therapy: is the future non-viral? In this episode, Valeria Annibaldi and Andrea Toell discuss the types and benefits of non-viral methods for ex vivo cell and gene therapy in addition to the readiness of electroporation-based technologies for use in GMP manufacturing.  To read this interview and access lots more content, visit the Cell and Gene Therapy Insights website ]]></itunes:summary>
    <description><![CDATA[<p>Non-viral methods for <em>ex vivo</em> cell &amp; gene therapy: is the future non-viral? In this episode, Valeria Annibaldi and Andrea Toell discuss the types and benefits of non-viral methods for <em>ex vivo</em> cell and gene therapy in addition to the readiness of electroporation-based technologies for use in GMP manufacturing.<br/><br/>To read this <a href='https://insights.bio/cell-and-gene-therapy-insights/journal/article/2840/Non-viral-methods-for-emex-vivo-em-cell-gene-therapy-is-the-future-non-viral'>interview and access lots</a> more content, visit the <em>Cell and Gene Therapy Insights</em> website</p>]]></description>
    <content:encoded><![CDATA[<p>Non-viral methods for <em>ex vivo</em> cell &amp; gene therapy: is the future non-viral? In this episode, Valeria Annibaldi and Andrea Toell discuss the types and benefits of non-viral methods for <em>ex vivo</em> cell and gene therapy in addition to the readiness of electroporation-based technologies for use in GMP manufacturing.<br/><br/>To read this <a href='https://insights.bio/cell-and-gene-therapy-insights/journal/article/2840/Non-viral-methods-for-emex-vivo-em-cell-gene-therapy-is-the-future-non-viral'>interview and access lots</a> more content, visit the <em>Cell and Gene Therapy Insights</em> website</p>]]></content:encoded>
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    <itunes:author>Valeria Annibaldi and Andrea Toell</itunes:author>
    <guid isPermaLink="false">Buzzsprout-12952111</guid>
    <pubDate>Wed, 31 May 2023 10:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/12952111/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Non-viral methods for ex vivo cell &amp; gene therapy: is the future non-viral?" />
  <psc:chapter start="1:51" title="What non-viral methods are used in the space, and do you see their use evolving? " />
  <psc:chapter start="4:20" title="What are the advantages and disadvantages of utilizing non-viral technology for ex vivo cell therapy?" />
  <psc:chapter start="8:07" title="How can the challenge of transfecting cell types using non-viral means be overcome?" />
  <psc:chapter start="9:50" title="What non-viral gene transfer technology does Lonza offer? " />
  <psc:chapter start="12:11" title="What advantages does an electroporation-based method offer? " />
  <psc:chapter start="15:57" title="Is electroporation-based technology scalable to meet the needs of the industry? " />
  <psc:chapter start="17:54" title="What non-viral technologies are being used in clinical or commercial applications based on ex vivo modifications? " />
  <psc:chapter start="19:01" title="What are your predictions for the future of this space? " />
</psc:chapters>
    <itunes:duration>1297</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>5</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Solving challenges in cell therapy clinical trials &amp; effectively delivering complex studies in advanced therapeutics</itunes:title>
    <title>Solving challenges in cell therapy clinical trials &amp; effectively delivering complex studies in advanced therapeutics</title>
    <itunes:summary><![CDATA[Cell therapy clinical trials pose a variety of complex challenges. Logistics with cell harvesting, manufacturing, shipments back to sites, patient safety, changing standard-of-care treatments, and patient enrolment due to competing trials can all impact study timelines. In this episode, Vito Romita and Jai Balkissoon outline key obstacles for developing cell therapies in oncology, and provide their insights on overcoming them in order to increase patient access and design safer trials.  To re...]]></itunes:summary>
    <description><![CDATA[<p>Cell therapy clinical trials pose a variety of complex challenges. Logistics with cell harvesting, manufacturing, shipments back to sites, patient safety, changing standard-of-care treatments, and patient enrolment due to competing trials can all impact study timelines. In this episode, Vito Romita and Jai Balkissoon outline key obstacles for developing cell therapies in oncology, and provide their insights on overcoming them in order to increase patient access and design safer trials.<br/><br/>To <a href='https://www.insights.bio/immuno-oncology-insights/journal/article/2788/Solving-challenges-in-cell-therapy-clinical-trials-effectively-delivering-complex-studies-in-advanced-therapeutics'>read this interview</a> and access lots more content, visit the <em>Cell and Gene Therapy Insights</em> website<br/><br/></p>]]></description>
    <content:encoded><![CDATA[<p>Cell therapy clinical trials pose a variety of complex challenges. Logistics with cell harvesting, manufacturing, shipments back to sites, patient safety, changing standard-of-care treatments, and patient enrolment due to competing trials can all impact study timelines. In this episode, Vito Romita and Jai Balkissoon outline key obstacles for developing cell therapies in oncology, and provide their insights on overcoming them in order to increase patient access and design safer trials.<br/><br/>To <a href='https://www.insights.bio/immuno-oncology-insights/journal/article/2788/Solving-challenges-in-cell-therapy-clinical-trials-effectively-delivering-complex-studies-in-advanced-therapeutics'>read this interview</a> and access lots more content, visit the <em>Cell and Gene Therapy Insights</em> website<br/><br/></p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/12664920-solving-challenges-in-cell-therapy-clinical-trials-effectively-delivering-complex-studies-in-advanced-therapeutics.mp3" length="18039713" type="audio/mpeg" />
    <itunes:author>Vito Romita and Jai Balkissoon</itunes:author>
    <guid isPermaLink="false">Buzzsprout-12664920</guid>
    <pubDate>Mon, 17 Apr 2023 11:00:00 +0000</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="Solving challenges in cell therapy clinical trials &amp; effectively delivering complex studies in advanced therapeutics" />
  <psc:chapter start="1:59" title="What do you see as the three most important challenges with the current development of cell therapies in oncology?  " />
  <psc:chapter start="8:47" title="What can industry leaders, stakeholders and sponsors do to improve patient access for cell and gene therapy clinical trials? " />
  <psc:chapter start="20:20" title="How can we make complex cell and gene therapy trials more understandable to patients and their primary caregivers? " />
  <psc:chapter start="22:48" title="Finally, what can be done to help design safer cell therapy trials? " />
</psc:chapters>
    <itunes:duration>1500</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>4</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>true</itunes:explicit>
  </item>
  <item>
    <itunes:title>Shear ignorance? Think again: breaking the perception of shear within viral vector manufacturing</itunes:title>
    <title>Shear ignorance? Think again: breaking the perception of shear within viral vector manufacturing</title>
    <itunes:summary><![CDATA[The tangential flow filtration (TFF) unit operation in viral vector manufacturing is a critical step on the path to commercialization. In this episode, Merck viral vector experts Ratish Krishnan and Akshat Gupta discuss best practices – and common misconceptions – when establishing process conditions and utilizing different TFF device formats.   ]]></itunes:summary>
    <description><![CDATA[<p>The tangential flow filtration (TFF) unit operation in viral vector manufacturing is a critical step on the path to commercialization. In this episode, Merck viral vector experts Ratish Krishnan and Akshat Gupta discuss best practices – and common misconceptions – when establishing process conditions and utilizing different TFF device formats.  </p>]]></description>
    <content:encoded><![CDATA[<p>The tangential flow filtration (TFF) unit operation in viral vector manufacturing is a critical step on the path to commercialization. In this episode, Merck viral vector experts Ratish Krishnan and Akshat Gupta discuss best practices – and common misconceptions – when establishing process conditions and utilizing different TFF device formats.  </p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/12600970-shear-ignorance-think-again-breaking-the-perception-of-shear-within-viral-vector-manufacturing.mp3" length="13061573" type="audio/mpeg" />
    <itunes:author>Ratish Krishnan and Akshat Gupta</itunes:author>
    <guid isPermaLink="false">Buzzsprout-12600970</guid>
    <pubDate>Thu, 06 Apr 2023 14:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/12600970/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Shear ignorance? Think again: breaking the perception of shear within viral vector manufacturing" />
  <psc:chapter start="1:03" title="How is TFF used in viral vector manufacturing?" />
  <psc:chapter start="3:06" title="What are the main types of TFF used in viral vector purification?" />
  <psc:chapter start="6:53" title="What are the key factors when it comes to designing a TFF step?" />
  <psc:chapter start="11:06" title="What are some common misconceptions regarding TFF?" />
  <psc:chapter start="13:50" title="How are your teams working to overcome negative perceptions?" />
</psc:chapters>
    <itunes:duration>1085</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>3</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Challenges in cryogenic storage containers for cell and gene therapy</itunes:title>
    <title>Challenges in cryogenic storage containers for cell and gene therapy</title>
    <itunes:summary><![CDATA[Current options for cryogenic storage containers in cell and gene therapy are limited in their functionality as the industry continues to move towards increased scale and automation. In this episode, Sean Werner and Alex Sargent address specific challenges with current optionality, while also considering what future innovations in this area might look like.  To read this interview and access lots more content, visit the Cell and Gene Therapy Insights website   ]]></itunes:summary>
    <description><![CDATA[<p><b>Current options for cryogenic storage containers in cell and gene therapy are limited in their functionality as the industry continues to move towards increased scale and automation. In this episode, Sean Werner and Alex Sargent address specific challenges with current optionality, while also considering what future innovations in this area might look like.<br/><br/>To</b><a href='https://insights.bio/cell-and-gene-therapy-insights/journal/article/2764/Challenges-in-cryogenic-storage-containers-for-cell-gene-therapy'><b> read this interview</b></a><b> and access lots more content, visit the</b><b><em> Cell and Gene Therapy Insights</em></b><b> website<br/></b><br/></p>]]></description>
    <content:encoded><![CDATA[<p><b>Current options for cryogenic storage containers in cell and gene therapy are limited in their functionality as the industry continues to move towards increased scale and automation. In this episode, Sean Werner and Alex Sargent address specific challenges with current optionality, while also considering what future innovations in this area might look like.<br/><br/>To</b><a href='https://insights.bio/cell-and-gene-therapy-insights/journal/article/2764/Challenges-in-cryogenic-storage-containers-for-cell-gene-therapy'><b> read this interview</b></a><b> and access lots more content, visit the</b><b><em> Cell and Gene Therapy Insights</em></b><b> website<br/></b><br/></p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/12493011-challenges-in-cryogenic-storage-containers-for-cell-and-gene-therapy.mp3" length="12861947" type="audio/mpeg" />
    <itunes:author>Sean Werner and Alex Sargent</itunes:author>
    <guid isPermaLink="false">Buzzsprout-12493011</guid>
    <pubDate>Wed, 22 Mar 2023 12:00:00 +0000</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="Challenges in cryogenic storage containers for cell and gene therapy" />
  <psc:chapter start="2:12" title="1.	How have we landed on the current landscape of options for cryogenic storage containers used in the cell and gene therapy space?  " />
  <psc:chapter start="3:55" title="2.	Where do the current offerings fall short as the cell and gene therapy industry continues to grow? " />
  <psc:chapter start="7:30" title="3.	What will be negative impacts of continuing with these solutions as opposed to developing containers more specific to industry needs? " />
  <psc:chapter start="10:50" title="4.	What should the cryogenic container of the future look like? What are the most important considerations or features? " />
  <psc:chapter start="13:35" title="5.	What additional considerations need to be addressed if truly allogeneic therapies, with tens of thousands of doses, are found to be more universally successful? " />
</psc:chapters>
    <itunes:duration>1068</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>2</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Maximizing Efficiency and Flexibility in Viral Vector Manufacturing Scale-up</itunes:title>
    <title>Maximizing Efficiency and Flexibility in Viral Vector Manufacturing Scale-up</title>
    <itunes:summary><![CDATA[Four viral vector experts from diverse groups within Pall Corporation’s gene therapy manufacturing organization – Denis Kole, Jon Petrone, Marc Bisschops and Nathan Hazi – join BioInsights to share insights in hot topics for the field, including optimizing upstream process yield and titer, full/empty/partially full capsid separation, and platform process development. ]]></itunes:summary>
    <description><![CDATA[<p>Four viral vector experts from diverse groups within Pall Corporation’s gene therapy manufacturing organization – Denis Kole, Jon Petrone, Marc Bisschops and Nathan Hazi – join BioInsights to share insights in hot topics for the field, including optimizing upstream process yield and titer, full/empty/partially full capsid separation, and platform process development.</p>]]></description>
    <content:encoded><![CDATA[<p>Four viral vector experts from diverse groups within Pall Corporation’s gene therapy manufacturing organization – Denis Kole, Jon Petrone, Marc Bisschops and Nathan Hazi – join BioInsights to share insights in hot topics for the field, including optimizing upstream process yield and titer, full/empty/partially full capsid separation, and platform process development.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/12360123-maximizing-efficiency-and-flexibility-in-viral-vector-manufacturing-scale-up.mp3" length="26785816" type="audio/mpeg" />
    <itunes:author>Denis Kole, Jon Petrone, Marc Bisschops and Nathan Hazi</itunes:author>
    <guid isPermaLink="false">Buzzsprout-12360123</guid>
    <pubDate>Thu, 02 Mar 2023 11:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/12360123/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Maximizing Efficiency and Flexibility in Viral Vector Manufacturing Scale-up" />
  <psc:chapter start="0:54" title="Key current challenges in viral vector processing " />
  <psc:chapter start="6:26" title="Technological advancements in upstream processing" />
  <psc:chapter start="9:13" title="Ensuring optimal consistency through scale-up/out" />
  <psc:chapter start="12:11" title="What’s next for transient transfection?" />
  <psc:chapter start="15:23" title="Enabling viral vector process intensification" />
  <psc:chapter start="20:20" title="How well are the current range of purification technologies performing?" />
  <psc:chapter start="23:48" title="How best to improve full/empty/partially full capsid ratio?" />
  <psc:chapter start="27:43" title="Standardized vector platform processes" />
  <psc:chapter start="30:01" title="Minimum process parameters needed to build a platform viral vector process" />
  <psc:chapter start="33:16" title="Automating gene therapy manufacture for rare disease indications " />
</psc:chapters>
    <itunes:duration>2229</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>2</itunes:season>
    <itunes:episode>1</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Improvement of viral vector purification using Mustang Q membrane chromatography </itunes:title>
    <title>Improvement of viral vector purification using Mustang Q membrane chromatography </title>
    <itunes:summary><![CDATA[Saadia Zakai and Mark Schofield of Pall join Hélène Lebas of leading viral vector CDMO, Yposkesi, to discuss key current trends and challenges in AAV and lentiviral vector manufacturing, with a particular focus on the cutting edge in lentiviral vector and adeno-associated viral (AAV) vector purification tools.   ]]></itunes:summary>
    <description><![CDATA[<p>Saadia Zakai and Mark Schofield of Pall join Hélène Lebas of leading viral vector CDMO, Yposkesi, to discuss key current trends and challenges in AAV and lentiviral vector manufacturing, with a particular focus on the cutting edge in lentiviral vector and adeno-associated viral (AAV) vector purification tools.</p><p> </p>]]></description>
    <content:encoded><![CDATA[<p>Saadia Zakai and Mark Schofield of Pall join Hélène Lebas of leading viral vector CDMO, Yposkesi, to discuss key current trends and challenges in AAV and lentiviral vector manufacturing, with a particular focus on the cutting edge in lentiviral vector and adeno-associated viral (AAV) vector purification tools.</p><p> </p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11863230-improvement-of-viral-vector-purification-using-mustang-q-membrane-chromatography.mp3" length="23378276" type="audio/mpeg" />
    <itunes:author>Saadia Zakai, Mark Schofield,  Hélène Lebas</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11863230</guid>
    <pubDate>Tue, 13 Dec 2022 10:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11863230/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Improvement of viral vector purification using Mustang Q membrane chromatography " />
  <psc:chapter start="0:57" title="Introducing the panellists" />
  <psc:chapter start="4:37" title="Key current trends and challenges in AAV and lentiviral vector manufacturing" />
  <psc:chapter start="10:27" title="Characterizing the current viral vector purification toolkits for lentivirus and AAV" />
  <psc:chapter start="14:46" title="What advantages do membrane chromatography and the Mustang Q system offer?" />
  <psc:chapter start="17:39" title="Considerations for Mustang Q application and performance in lentiviral purification" />
  <psc:chapter start="21:34" title="Mustang Q in application for AAV full-empty capsid separation" />
  <psc:chapter start="26:32" title="Will regulators set a minimum specification for the percentage of full AAV capsids?" />
  <psc:chapter start="29:05" title="Parting advice on application of membrane chromatography systems " />
</psc:chapters>
    <itunes:duration>1945</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>21</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Shear ignorance? Think again: breaking the perception of shear within viral vector manufacturing</itunes:title>
    <title>Shear ignorance? Think again: breaking the perception of shear within viral vector manufacturing</title>
    <itunes:summary><![CDATA[The tangential flow filtration (TFF) unit operation in viral vector manufacturing is a critical step on the path to commercialization. In this episode, Merck viral vector experts Ratish Krishnan and Akshat Gupta discuss best practices – and common misconceptions – when establishing process conditions and utilizing different TFF device formats.   ]]></itunes:summary>
    <description><![CDATA[<p>The tangential flow filtration (TFF) unit operation in viral vector manufacturing is a critical step on the path to commercialization. In this episode, Merck viral vector experts Ratish Krishnan and Akshat Gupta discuss best practices – and common misconceptions – when establishing process conditions and utilizing different TFF device formats.  </p>]]></description>
    <content:encoded><![CDATA[<p>The tangential flow filtration (TFF) unit operation in viral vector manufacturing is a critical step on the path to commercialization. In this episode, Merck viral vector experts Ratish Krishnan and Akshat Gupta discuss best practices – and common misconceptions – when establishing process conditions and utilizing different TFF device formats.  </p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11662629-shear-ignorance-think-again-breaking-the-perception-of-shear-within-viral-vector-manufacturing.mp3" length="13061581" type="audio/mpeg" />
    <itunes:author>Ratish Krishnan, Akshat Gupta</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11662629</guid>
    <pubDate>Wed, 09 Nov 2022 14:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11662629/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Shear ignorance? Think again: breaking the perception of shear within viral vector manufacturing" />
  <psc:chapter start="1:03" title="How is TFF used in viral vector manufacturing?  " />
  <psc:chapter start="3:06" title="What are the main types of TFF used in viral vector purification?  " />
  <psc:chapter start="6:53" title="What are the key factors when it comes to designing a TFF step? " />
  <psc:chapter start="11:06" title="What are some common misconceptions regarding TFF? " />
  <psc:chapter start="13:50" title="How are your teams working to overcome negative perceptions? " />
</psc:chapters>
    <itunes:duration>1085</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>20</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>CAR-T cells: from cancer to autoimmunity</itunes:title>
    <title>CAR-T cells: from cancer to autoimmunity</title>
    <itunes:summary><![CDATA[Professor Dimitrios Mougiakakos is the director of the Hematology and Oncology department at the Otto-von-Guericke University in Magdeburg, Germany. In this episode, he joins us to discuss the exciting potential for CAR T cell therapy for autoimmune disease and how his team has approached GMP manufacturing in the clinical setting. He explains the challenges faced in setting up cell therapy for systemic lupus erythematosus (SLE), and the future of cell and gene therapy in different indications. ]]></itunes:summary>
    <description><![CDATA[<p>Professor Dimitrios Mougiakakos is the director of the Hematology and Oncology department at the Otto-von-Guericke University in Magdeburg, Germany. In this episode, he joins us to discuss the exciting potential for CAR T cell therapy for autoimmune disease and how his team has approached GMP manufacturing in the clinical setting. He explains the challenges faced in setting up cell therapy for systemic lupus erythematosus (SLE), and the future of cell and gene therapy in different indications.</p>]]></description>
    <content:encoded><![CDATA[<p>Professor Dimitrios Mougiakakos is the director of the Hematology and Oncology department at the Otto-von-Guericke University in Magdeburg, Germany. In this episode, he joins us to discuss the exciting potential for CAR T cell therapy for autoimmune disease and how his team has approached GMP manufacturing in the clinical setting. He explains the challenges faced in setting up cell therapy for systemic lupus erythematosus (SLE), and the future of cell and gene therapy in different indications.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11485485-car-t-cells-from-cancer-to-autoimmunity.mp3" length="21662053" type="audio/mpeg" />
    <itunes:author>Professor Dimitrios Mougiakakos</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11485485</guid>
    <pubDate>Wed, 12 Oct 2022 14:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11485485/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="CAR-T cells: from cancer to autoimmunity" />
  <psc:chapter start="1:01" title="How did you first become interested in cell and gene therapy?" />
  <psc:chapter start="3:14" title="What led to your recent work treating lupus?" />
  <psc:chapter start="5:55" title="What is the benefit of using CAR T cell therapy to target B cells in lupus?" />
  <psc:chapter start="11:57" title="What have been the results of the human trials so far?" />
  <psc:chapter start="19:06" title="What were the operational challenges of setting up cell therapy in your clinical setting?" />
  <psc:chapter start="21:29" title="How did advance in technologies help you overcome those challenges?" />
  <psc:chapter start="23:15" title="Do we need decentralized CAR T cell production in the academic setting?" />
  <psc:chapter start="25:02" title="What challenges remain? Where could technology make an impact?" />
  <psc:chapter start="30:39" title="Where is the brightest future for cell and gene therapies?" />
</psc:chapters>
    <itunes:duration>1802</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>19</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Tales, tips &amp; teachable moments from applications support veterans</itunes:title>
    <title>Tales, tips &amp; teachable moments from applications support veterans</title>
    <itunes:summary><![CDATA[Cell and gene therapy scientists are under increasing pressure to achieve results faster and produce cells and cell products more cost-efficiently. Field applications scientists from their major suppliers can provide invaluable support, helping to optimize processes, utilize new platforms and technologies more effectively, and avoid costly errors. In this podcast, three veteran Field Applications Scientists from Corning Life Sciences - Austin Mogen, Catherine Siler, and Chris Suarez - share t...]]></itunes:summary>
    <description><![CDATA[<p>Cell and gene therapy scientists are under increasing pressure to achieve results faster and produce cells and cell products more cost-efficiently. Field applications scientists from their major suppliers can provide invaluable support, helping to optimize processes, utilize new platforms and technologies more effectively, and avoid costly errors. In this podcast, three veteran Field Applications Scientists from Corning Life Sciences - Austin Mogen, Catherine Siler, and Chris Suarez - share their expertise and lessons learned over decades of experience. </p>]]></description>
    <content:encoded><![CDATA[<p>Cell and gene therapy scientists are under increasing pressure to achieve results faster and produce cells and cell products more cost-efficiently. Field applications scientists from their major suppliers can provide invaluable support, helping to optimize processes, utilize new platforms and technologies more effectively, and avoid costly errors. In this podcast, three veteran Field Applications Scientists from Corning Life Sciences - Austin Mogen, Catherine Siler, and Chris Suarez - share their expertise and lessons learned over decades of experience. </p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11481004-tales-tips-teachable-moments-from-applications-support-veterans.mp3" length="18299410" type="audio/mpeg" />
    <itunes:author>Austin Mogen, Catherine Siler and Chris Suarez</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11481004</guid>
    <pubDate>Tue, 11 Oct 2022 20:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11481004/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Tales, tips &amp; teachable moments from applications support veterans" />
  <psc:chapter start="1:47" title="What are some common missteps, and what can we learn from these?" />
  <psc:chapter start="9:15" title="What is the most rewarding thing you have done in support of a customer?" />
  <psc:chapter start="10:45" title="What would be your initial advice for a customer beginning a process?" />
  <psc:chapter start="11:50" title="How should a customer start troubleshooting divergent results?" />
  <psc:chapter start="13:43" title="How did the pandemic change engagement with customers?" />
  <psc:chapter start="18:38" title="When should a customer engage with their supplier’s field support team?" />
  <psc:chapter start="22:50" title="What is your top piece of advice?" />
</psc:chapters>
    <itunes:duration>1521</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>18</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Access to vaccines: how can we leverage technology innovations to achieve greater vaccine equity?</itunes:title>
    <title>Access to vaccines: how can we leverage technology innovations to achieve greater vaccine equity?</title>
    <itunes:summary><![CDATA[Fatema Kazi works for the WHO, where she helps to assess the public health value of vaccine products and technologies in routine, campaign, and outbreak settings. We caught up with her to discuss how innovations in vaccine technology can help get vaccines to the people who need them. ]]></itunes:summary>
    <description><![CDATA[<p>Fatema Kazi works for the WHO, where she helps to assess the public health value of vaccine products and technologies in routine, campaign, and outbreak settings. We caught up with her to discuss how innovations in vaccine technology can help get vaccines to the people who need them.</p>]]></description>
    <content:encoded><![CDATA[<p>Fatema Kazi works for the WHO, where she helps to assess the public health value of vaccine products and technologies in routine, campaign, and outbreak settings. We caught up with her to discuss how innovations in vaccine technology can help get vaccines to the people who need them.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11413328-access-to-vaccines-how-can-we-leverage-technology-innovations-to-achieve-greater-vaccine-equity.mp3" length="13439346" type="audio/mpeg" />
    <itunes:author>Fatema Kazi</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11413328</guid>
    <pubDate>Fri, 30 Sep 2022 12:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11413328/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="What’s next?" />
  <psc:chapter start="0:00" title="Is the future needle-free?" />
  <psc:chapter start="0:00" title="When will we see MAPs on the market?" />
  <psc:chapter start="1:06" title="What sparked your interest in vaccines?" />
  <psc:chapter start="4:16" title="What is your role at WHO?" />
  <psc:chapter start="8:52" title="Can technology innovations improve vaccine delivery &amp; equity?" />
  <psc:chapter start="13:05" title="Most impactful technology to emerge during the pandemic?" />
</psc:chapters>
    <itunes:duration>1116</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>17</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>De-risk &amp; accelerate the drug development process for gene therapy</itunes:title>
    <title>De-risk &amp; accelerate the drug development process for gene therapy</title>
    <itunes:summary><![CDATA[In today’s challenging financial environment, it is more important than ever to get key biotech business decisions right first time. One of the most important and topical of these is the choice of CDMO partner. Dr Kim Watanabe, General Manager and Site Head for Patheon Translational Services, a part of the Thermo Fisher Scientific pharma services contract development and manufacturing organizational arm, joins BioInsights to share her advice and insights into optimizing outsourcing strategy. ]]></itunes:summary>
    <description><![CDATA[<p>In today’s challenging financial environment, it is more important than ever to get key biotech business decisions right first time. One of the most important and topical of these is the choice of CDMO partner. Dr Kim Watanabe, General Manager and Site Head for Patheon Translational Services, a part of the Thermo Fisher Scientific pharma services contract development and manufacturing organizational arm, joins BioInsights to share her advice and insights into optimizing outsourcing strategy.</p>]]></description>
    <content:encoded><![CDATA[<p>In today’s challenging financial environment, it is more important than ever to get key biotech business decisions right first time. One of the most important and topical of these is the choice of CDMO partner. Dr Kim Watanabe, General Manager and Site Head for Patheon Translational Services, a part of the Thermo Fisher Scientific pharma services contract development and manufacturing organizational arm, joins BioInsights to share her advice and insights into optimizing outsourcing strategy.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11405679-de-risk-accelerate-the-drug-development-process-for-gene-therapy.mp3" length="8328849" type="audio/mpeg" />
    <itunes:author>Dr Kim Watanabe</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11405679</guid>
    <pubDate>Thu, 29 Sep 2022 07:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11405679/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="De-risk &amp; accelerate the drug development process for gene therapy" />
  <psc:chapter start="1:04" title="Key high level trends impacting gene therapy biotech decision-making around outsourcing" />
  <psc:chapter start="3:54" title="When should small biotechs engage with CDMOs?" />
  <psc:chapter start="5:24" title="What can CDMOs do to provide bits of support to biotech until they are ready?" />
  <psc:chapter start="7:15" title="Solve the challenges of doing business today and addressing concerns of the future?" />
  <psc:chapter start="8:50" title="What should be considered when choosing a CDMO partner?  " />
</psc:chapters>
    <itunes:duration>691</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>17</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Working Together to Safely Advance Cell &amp; Gene Therapies</itunes:title>
    <title>Working Together to Safely Advance Cell &amp; Gene Therapies</title>
    <itunes:summary><![CDATA[Drug development is a costly and time-consuming process associated with a significant attrition rate in the clinic. Safety is an important factor in this, and is a particular issue for cell and gene therapies. A panel moderated by Dr John Maher of King’s College London and Leucid Bio, and featuring Dr Alastair King, Dr Francisca Neethling, and Dr Andrea Bisso, discuss this highly topical barrier to the further clinical and commercial success of the field.   ]]></itunes:summary>
    <description><![CDATA[<p>Drug development is a costly and time-consuming process associated with a significant attrition rate in the clinic. Safety is an important factor in this, and is a particular issue for cell and gene therapies. A panel moderated by Dr John Maher of King’s College London and Leucid Bio, and featuring Dr Alastair King, Dr Francisca Neethling, and Dr Andrea Bisso, discuss this highly topical barrier to the further clinical and commercial success of the field.<br/><br/></p>]]></description>
    <content:encoded><![CDATA[<p>Drug development is a costly and time-consuming process associated with a significant attrition rate in the clinic. Safety is an important factor in this, and is a particular issue for cell and gene therapies. A panel moderated by Dr John Maher of King’s College London and Leucid Bio, and featuring Dr Alastair King, Dr Francisca Neethling, and Dr Andrea Bisso, discuss this highly topical barrier to the further clinical and commercial success of the field.<br/><br/></p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11392262-working-together-to-safely-advance-cell-gene-therapies.mp3" length="43243400" type="audio/mpeg" />
    <itunes:author>Dr John Maher of King’s College London and Leucid Bio, and featuring Dr Alastair King, Dr Francisca Neethling, and Dr Andrea Bisso</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11392262</guid>
    <pubDate>Tue, 27 Sep 2022 11:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11392262/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Working Together to Safely Advance Cell &amp; Gene Therapies" />
  <psc:chapter start="2:45" title="What are the primary safety considerations at the preclinical stage?" />
  <psc:chapter start="11:12" title="How do we create more predictive approaches for advanced therapies?" />
  <psc:chapter start="19:24" title="What will be the greatest challenges to implementing non-animal alternatives in preclinical testing?" />
  <psc:chapter start="30:04" title="How to modify existing platforms?" />
  <psc:chapter start="41:59" title="How to choose an outsourcing partner, and what is the primary role of the CRO?" />
  <psc:chapter start="50:45" title="Do virtual companies have special needs regarding assay and safety considerations?" />
  <psc:chapter start="55:10" title="How can we work together to safely advance cell and gene therapies? " />
</psc:chapters>
    <itunes:duration>3600</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>16</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
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  <item>
    <itunes:title>Learning from pediatric CAR-T development: insights from manufacturing unique patient doses</itunes:title>
    <title>Learning from pediatric CAR-T development: insights from manufacturing unique patient doses</title>
    <itunes:summary><![CDATA[What valuable experiences from first generation cell therapies can the industry carry forward and apply to other indications, such as solid tumors? In this episode, Sean Werner and Chris Brown explore the most important lessons the industry has gleaned from pediatrics, and how they can inform the future of cell therapy manufacturing. ]]></itunes:summary>
    <description><![CDATA[<p>What valuable experiences from first generation cell therapies can the industry carry forward and apply to other indications, such as solid tumors? In this episode, Sean Werner and Chris Brown explore the most important lessons the industry has gleaned from pediatrics, and how they can inform the future of cell therapy manufacturing.</p>]]></description>
    <content:encoded><![CDATA[<p>What valuable experiences from first generation cell therapies can the industry carry forward and apply to other indications, such as solid tumors? In this episode, Sean Werner and Chris Brown explore the most important lessons the industry has gleaned from pediatrics, and how they can inform the future of cell therapy manufacturing.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11385107-learning-from-pediatric-car-t-development-insights-from-manufacturing-unique-patient-doses.mp3" length="15103974" type="audio/mpeg" />
    <itunes:author>Sean Werner and Chris Brown</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11385107</guid>
    <pubDate>Mon, 26 Sep 2022 11:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11385107/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Learning from pediatric CAR-T development: insights from manufacturing unique patient doses" />
  <psc:chapter start="2:01" title="Firstly, can you both tell me a bit about the current work you do? " />
  <psc:chapter start="2:34" title="What lessons has the cell and gene therapy industry learned from pediatric therapies that can be applied to developing cell therapies for other indications? " />
  <psc:chapter start="4:14" title="When it comes to the development of cell therapies for these indications, what represents the cutting-edge regarding tools and technology? " />
  <psc:chapter start="7:26" title="What are the biggest current challenges regarding cost and funding? " />
  <psc:chapter start="11:15" title="From a supplier perspective, what has worked well – or doesn’t work well – when trying to solve customer challenges? " />
  <psc:chapter start="15:30" title="Looking to the future, what are the biggest lessons gleaned from first generation cell therapies? " />
</psc:chapters>
    <itunes:duration>1255</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>15</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Insights into the editing of the human genome: where can novel non-viral polymeric delivery agents take us</itunes:title>
    <title>Insights into the editing of the human genome: where can novel non-viral polymeric delivery agents take us</title>
    <itunes:summary><![CDATA[Tom Foti (Vice President and General Manager of the Protein Business Unit, Aldevron) and Dr Kris Saha (Associate Professor of Biomedical Engineering and Medical History and Bioethics, University of Wisconsin-Madison) discuss ongoing work in Dr Saha’s lab to harness different types of HDR templates in order to build cutting-edge systems with the potential to enable point-of-care cell and gene therapy manufacture.  ]]></itunes:summary>
    <description><![CDATA[<p>Tom Foti (Vice President and General Manager of the Protein Business Unit, Aldevron) and Dr Kris Saha (Associate Professor of Biomedical Engineering and Medical History and Bioethics, University of Wisconsin-Madison) discuss ongoing work in Dr Saha’s lab to harness different types of HDR templates in order to build cutting-edge systems with the potential to enable point-of-care cell and gene therapy manufacture. </p>]]></description>
    <content:encoded><![CDATA[<p>Tom Foti (Vice President and General Manager of the Protein Business Unit, Aldevron) and Dr Kris Saha (Associate Professor of Biomedical Engineering and Medical History and Bioethics, University of Wisconsin-Madison) discuss ongoing work in Dr Saha’s lab to harness different types of HDR templates in order to build cutting-edge systems with the potential to enable point-of-care cell and gene therapy manufacture. </p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11302280-insights-into-the-editing-of-the-human-genome-where-can-novel-non-viral-polymeric-delivery-agents-take-us.mp3" length="20335713" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11302280</guid>
    <pubDate>Mon, 12 Sep 2022 08:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11302280/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Insights into the editing of the human genome: where can novel non-viral polymeric delivery agents take us" />
  <psc:chapter start="1:23" title="Kris, tell us about your lab and the work you’re doing at the University of Wisconsin" />
  <psc:chapter start="7:27" title="How has Aldevron supported Kris’ work and how have both parties benefited?" />
  <psc:chapter start="9:28" title="Gene editing platforms, delivery technologies, in vivo cell tracking, and novel animal models - which of these is the biggest challenge and why?" />
  <psc:chapter start="14:00" title="What is the role of industry in tackling these challenges?" />
  <psc:chapter start="19:18" title="What is on the horizon for genomic medicine?" />
  <psc:chapter start="22:20" title="What is Danaher’s role in advancing genomic medicine?" />
</psc:chapters>
    <itunes:duration>1691</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>14</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Making the switch from autologous to allogeneic cell therapy</itunes:title>
    <title>Making the switch from autologous to allogeneic cell therapy</title>
    <itunes:summary></itunes:summary>
    <description></description>
    <content:encoded></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11288156-making-the-switch-from-autologous-to-allogeneic-cell-therapy.mp3" length="20136956" type="audio/mpeg" />
    <itunes:author>Elena Matsa &amp; Andy Holt</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11288156</guid>
    <pubDate>Fri, 09 Sep 2022 07:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11288156/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Making the switch from autologous to allogeneic cell therapy" />
  <psc:chapter start="1:24" title="To set the scene, could you firstly tell me a bit about your backgrounds, and your current work?  " />
  <psc:chapter start="5:05" title="What role do you predict induced pluripotent stem cells (iPSCs) will play in the future of cell therapy? " />
  <psc:chapter start="8:30" title="What are the key benefits of autologous versus allogeneic cell therapies?" />
  <psc:chapter start="14:06" title="What do you see as the biggest obstacles to successful iPSC-based allogeneic cell therapy development – and how can they be addressed? " />
  <psc:chapter start="20:02" title="What are the most important considerations for developing a successful cell therapy manufacturing process? " />
  <psc:chapter start="24:10" title="What is your key advice for making the change from autologous to allogeneic cell therapy development a practical reality? " />
</psc:chapters>
    <itunes:duration>1675</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>13</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Accelerating cures: funding stem cell innovation &amp; ideas in an evolving cell therapy space</itunes:title>
    <title>Accelerating cures: funding stem cell innovation &amp; ideas in an evolving cell therapy space</title>
    <itunes:summary><![CDATA[The Maryland Stem Cell Research Fund (MSCRF) is a well-established US state fund aimed specifically at driving the development of new medical strategies for the prevention, diagnosis, treatment and cure of human diseases, injuries, and conditions through human stem cells. Here, we discuss the MSCRF’s specific activities and goals with Executive Director, Dr Amrithar Jaishankar, and get her take on how best to develop collaborative research programs and promote commercialization of stem cell t...]]></itunes:summary>
    <description><![CDATA[<p>The Maryland Stem Cell Research Fund (MSCRF) is a well-established US state fund aimed specifically at driving the development of new medical strategies for the prevention, diagnosis, treatment and cure of human diseases, injuries, and conditions through human stem cells. Here, we discuss the MSCRF’s specific activities and goals with Executive Director, Dr Amrithar Jaishankar, and get her take on how best to develop collaborative research programs and promote commercialization of stem cell technologies.</p>]]></description>
    <content:encoded><![CDATA[<p>The Maryland Stem Cell Research Fund (MSCRF) is a well-established US state fund aimed specifically at driving the development of new medical strategies for the prevention, diagnosis, treatment and cure of human diseases, injuries, and conditions through human stem cells. Here, we discuss the MSCRF’s specific activities and goals with Executive Director, Dr Amrithar Jaishankar, and get her take on how best to develop collaborative research programs and promote commercialization of stem cell technologies.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11262544-accelerating-cures-funding-stem-cell-innovation-ideas-in-an-evolving-cell-therapy-space.mp3" length="11460720" type="audio/mpeg" />
    <itunes:author>Amrithar Jaishankar</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11262544</guid>
    <pubDate>Mon, 05 Sep 2022 13:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11262544/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Accelerating cures: funding stem cell innovation &amp; ideas in an evolving cell therapy space" />
  <psc:chapter start="1:25" title="What are you working on right now?" />
  <psc:chapter start="2:02" title="How and why did MSCRF get its start? " />
  <psc:chapter start="3:31" title="How have MSCRF’s goals and areas of activity evolved in recent times?" />
  <psc:chapter start="6:33" title="What drew you to your current role?" />
  <psc:chapter start="8:53" title="How does MSCRF keep innovation moving into and through the clinic?" />
  <psc:chapter start="10:35" title="Which stem cell therapy modalities/indications/platforms will drive the field forward?" />
  <psc:chapter start="13:21" title="What are some key goals and priorities for your work over the next 12-24 months?" />
</psc:chapters>
    <itunes:duration>952</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>12</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Insights into the editing of the human genome: where can novel non-viral polymeric delivery agents take us</itunes:title>
    <title>Insights into the editing of the human genome: where can novel non-viral polymeric delivery agents take us</title>
    <itunes:summary></itunes:summary>
    <description></description>
    <content:encoded></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11149115-insights-into-the-editing-of-the-human-genome-where-can-novel-non-viral-polymeric-delivery-agents-take-us.mp3" length="20334360" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11149115</guid>
    <pubDate>Tue, 16 Aug 2022 18:00:00 +0000</pubDate>
    <itunes:duration>1691</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>11</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Achieving better AAV vector productivity and product quality</itunes:title>
    <title>Achieving better AAV vector productivity and product quality</title>
    <itunes:summary><![CDATA[Transient transfection of plasmids into suspension HEK293 cells is still the most commonly used method for the production of recombinant adeno-associated virus (rAAV) gene therapies – in this episode, Diane Golebiowski and Marissa Stanvick discuss ways to optimize that process.     ]]></itunes:summary>
    <description><![CDATA[<p>Transient transfection of plasmids into suspension HEK293 cells is still the most commonly used method for the production of recombinant adeno-associated virus (rAAV) gene therapies – in this episode, Diane Golebiowski and Marissa Stanvick discuss ways to optimize that process. <br/><br/><br/></p>]]></description>
    <content:encoded><![CDATA[<p>Transient transfection of plasmids into suspension HEK293 cells is still the most commonly used method for the production of recombinant adeno-associated virus (rAAV) gene therapies – in this episode, Diane Golebiowski and Marissa Stanvick discuss ways to optimize that process. <br/><br/><br/></p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11086037-achieving-better-aav-vector-productivity-and-product-quality.mp3" length="13705490" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11086037</guid>
    <pubDate>Fri, 05 Aug 2022 10:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11086037/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Achieving better AAV vector productivity and product quality" />
  <psc:chapter start="1:46" title="1.	How important is plasmid design to vector productivity and quality? " />
  <psc:chapter start="5:48" title="2.	What were the biggest challenges you found with the design of the dual plasmids?" />
  <psc:chapter start="6:23" title="3.	And how important is rAAV sequence to vector productivity?" />
  <psc:chapter start="8:51" title="4.	What other areas did you focus on when trying to increase the bioreactor productivity? " />
  <psc:chapter start="13:34" title="5.	What areas are key to focus on for a successful scale up? " />
</psc:chapters>
    <itunes:duration>1139</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>10</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Partnering in life sciences: what is the ‘secret sauce’ for success? PART 2 </itunes:title>
    <title>Partnering in life sciences: what is the ‘secret sauce’ for success? PART 2 </title>
    <itunes:summary><![CDATA[Welcome to a 2-part series in which we identify and distill some key learnings for partnering success in today's life sciences sector.   Perhaps one of the most valuable take-aways from the COVID-19 pandemic response is the sheer scale of what may be achieved through effective collaboration. Over the next three episodes, we'll talk to a range of different stakeholders from across BioInsights' fields of focus, asking them to pass on their tips for what works and what doesn't in this crucial as...]]></itunes:summary>
    <description><![CDATA[<p>Welcome to a 2-part series in which we identify and distill some key learnings for partnering success in today&apos;s life sciences sector.<br/><br/></p><p>Perhaps one of the most valuable take-aways from the COVID-19 pandemic response is the sheer scale of what may be achieved through effective collaboration. Over the next three episodes, we&apos;ll talk to a range of different stakeholders from across BioInsights&apos; fields of focus, asking them to pass on their tips for what works and what doesn&apos;t in this crucial aspect. <br/><br/></p><p><b>Abi Pinchbeck</b>, Assistant Editor, <em>Immuno-oncology Insights</em>, speaks to <b>Arjun Goyal<br/></b><br/></p><p>In PART 2,  <b>Arjun Goyal</b>, co-founder and managing director of US-based life sciences venture capital firm Vida Ventures, provides a venture capitalist&apos;s perspective on licensing and partnering within immuno-oncology.<br/><br/></p>]]></description>
    <content:encoded><![CDATA[<p>Welcome to a 2-part series in which we identify and distill some key learnings for partnering success in today&apos;s life sciences sector.<br/><br/></p><p>Perhaps one of the most valuable take-aways from the COVID-19 pandemic response is the sheer scale of what may be achieved through effective collaboration. Over the next three episodes, we&apos;ll talk to a range of different stakeholders from across BioInsights&apos; fields of focus, asking them to pass on their tips for what works and what doesn&apos;t in this crucial aspect. <br/><br/></p><p><b>Abi Pinchbeck</b>, Assistant Editor, <em>Immuno-oncology Insights</em>, speaks to <b>Arjun Goyal<br/></b><br/></p><p>In PART 2,  <b>Arjun Goyal</b>, co-founder and managing director of US-based life sciences venture capital firm Vida Ventures, provides a venture capitalist&apos;s perspective on licensing and partnering within immuno-oncology.<br/><br/></p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/11025521-partnering-in-life-sciences-what-is-the-secret-sauce-for-success-part-2.mp3" length="14123493" type="audio/mpeg" />
    <itunes:image href="https://storage.buzzsprout.com/rrkkehfk8ohzst931qzhvf5oo2x8?.jpg" />
    <itunes:author>Arjun Goyal</itunes:author>
    <guid isPermaLink="false">Buzzsprout-11025521</guid>
    <pubDate>Mon, 25 Jul 2022 18:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/11025521/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Partnering in life sciences: what is the ‘secret sauce’ for success? PART 2 " />
  <psc:chapter start="1:19" title="What are the common pitfalls companies face when negotiating and then executing on licensing and partnering deals?" />
  <psc:chapter start="5:27" title="What are the key “do’s and don’t’s” for successful collaborations in I-O? " />
  <psc:chapter start="10:10" title="What particular considerations come into play in the I–O space?" />
  <psc:chapter start="13:26" title="What specific technology areas within this space present IP issues or considerations to potential collaborators, and why?  " />
  <psc:chapter start="16:48" title="This Podcast discusses the ‘Secret Sauce for Success’ – what are the main ingredients, for you? " />
</psc:chapters>
    <itunes:duration>1173</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>9</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Partnering in life sciences: what is the secret sauce for success? PART 1: The Big Pharma perspective</itunes:title>
    <title>Partnering in life sciences: what is the secret sauce for success? PART 1: The Big Pharma perspective</title>
    <itunes:summary><![CDATA[PART 1: The Big Pharma Perspective  Welcome to a 2-part series in which we identify and distill some key learnings for partnering success in today's life sciences sector.  Perhaps one of the most valuable take-aways from the COVID-19 pandemic response is the sheer scale of what may be achieved through effective collaboration. Over the next three episodes, we'll talk to a range of different stakeholders, asking them to pass on their tips for what works and what doesn't in this crucial aspect. ...]]></itunes:summary>
    <description><![CDATA[<p><b>PART 1: The Big Pharma Perspective<br/><br/></b>Welcome to a 2-part series in which we identify and distill some key learnings for partnering success in today&apos;s life sciences sector.<br/><br/>Perhaps one of the most valuable take-aways from the COVID-19 pandemic response is the sheer scale of what may be achieved through effective collaboration. Over the next three episodes, we&apos;ll talk to a range of different stakeholders, asking them to pass on their tips for what works and what doesn&apos;t in this crucial aspect.<br/><br/>In this first episode, <b>Dr Marianne De Backer, </b>a Member of the Executive Committee and Executive Vice President of Strategy, Business Development &amp; Licensing, and Open Innovation at Bayer Pharmaceuticals, shares her experience as a driving force behind Bayer’s significant recent moves in the cell and gene therapy area. </p>]]></description>
    <content:encoded><![CDATA[<p><b>PART 1: The Big Pharma Perspective<br/><br/></b>Welcome to a 2-part series in which we identify and distill some key learnings for partnering success in today&apos;s life sciences sector.<br/><br/>Perhaps one of the most valuable take-aways from the COVID-19 pandemic response is the sheer scale of what may be achieved through effective collaboration. Over the next three episodes, we&apos;ll talk to a range of different stakeholders, asking them to pass on their tips for what works and what doesn&apos;t in this crucial aspect.<br/><br/>In this first episode, <b>Dr Marianne De Backer, </b>a Member of the Executive Committee and Executive Vice President of Strategy, Business Development &amp; Licensing, and Open Innovation at Bayer Pharmaceuticals, shares her experience as a driving force behind Bayer’s significant recent moves in the cell and gene therapy area. </p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/10980642-partnering-in-life-sciences-what-is-the-secret-sauce-for-success-part-1-the-big-pharma-perspective.mp3" length="20597663" type="audio/mpeg" />
    <itunes:image href="https://storage.buzzsprout.com/lrv5cvh3ju7uzd1b07tup9fwdpw3?.jpg" />
    <itunes:author>Dr Marianne De Backer</itunes:author>
    <guid isPermaLink="false">Buzzsprout-10980642</guid>
    <pubDate>Mon, 18 Jul 2022 16:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/10980642/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Partnering in life sciences: what is the secret sauce for success? PART 1: The Big Pharma perspective" />
  <psc:chapter start="1:08" title="Q1. What are your personal highlights from your career" />
  <psc:chapter start="5:22" title="What are the chief considerations for this new way of working?" />
  <psc:chapter start="7:25" title="What are the drivers behind the acquisitions and partnerships Bayer has made over the past few years in the cell and gene therapy space?" />
  <psc:chapter start="18:28" title="Are there any specific considerations for partnering in the cell and gene therapy space?" />
  <psc:chapter start="22:25" title="How will investment trends impact the licensing and partnering in the M&amp;A environment?" />
  <psc:chapter start="26:10" title="In the coming 2 years, what are your key priorities in the advanced therapies field?" />
</psc:chapters>
    <itunes:duration>1713</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>8</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Where will tomorrow’s workforce come from? PART 4: Who are tomorrow’s cell and gene therapy workers?</itunes:title>
    <title>Where will tomorrow’s workforce come from? PART 4: Who are tomorrow’s cell and gene therapy workers?</title>
    <itunes:summary><![CDATA[PART 4: Who are tomorrow’s cell and gene therapy workers? Welcome to a 4-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment: “Where will tomorrow’s workforce come from?” The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade now, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase in activity from both investors and big pharma. But wi...]]></itunes:summary>
    <description><![CDATA[<p><b>PART 4: Who are tomorrow’s cell and gene therapy workers?</b></p><p>Welcome to a 4-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment: “Where will tomorrow’s workforce come from?”</p><p>The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade now, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase in activity from both investors and big pharma. But with this relentless pace of growth and innovation comes the fundamental challenge of developing a sufficiently large and skilled workforce to support and maintain the sector. </p><p>In this final episode, we look to the future of the cell and gene therapy workforce, exploring the motivations, skills, goals, and priorities of three individuals who are at various early stages of their careers in the sector –<b> PhD student Tiffany Hood, recent Masters graduate Lihi Livne, and Sebastian Rudden, who is in his final year as an undergrad at University College London</b>. </p>]]></description>
    <content:encoded><![CDATA[<p><b>PART 4: Who are tomorrow’s cell and gene therapy workers?</b></p><p>Welcome to a 4-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment: “Where will tomorrow’s workforce come from?”</p><p>The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade now, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase in activity from both investors and big pharma. But with this relentless pace of growth and innovation comes the fundamental challenge of developing a sufficiently large and skilled workforce to support and maintain the sector. </p><p>In this final episode, we look to the future of the cell and gene therapy workforce, exploring the motivations, skills, goals, and priorities of three individuals who are at various early stages of their careers in the sector –<b> PhD student Tiffany Hood, recent Masters graduate Lihi Livne, and Sebastian Rudden, who is in his final year as an undergrad at University College London</b>. </p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/10825937-where-will-tomorrow-s-workforce-come-from-part-4-who-are-tomorrow-s-cell-and-gene-therapy-workers.mp3" length="32445232" type="audio/mpeg" />
    <itunes:image href="https://storage.buzzsprout.com/aehy71n92j9u5u9toexf6x0ar1yz?.jpg" />
    <itunes:author>Tiffany Hood, Lihi Livne, and Sebastian Rudden</itunes:author>
    <guid isPermaLink="false">Buzzsprout-10825937</guid>
    <pubDate>Mon, 20 Jun 2022 21:00:00 +0000</pubDate>
    <podcast:soundbite startTime="14.235" duration="15.0" />
    <itunes:duration>2699</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>7</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Where will tomorrow’s workforce come from? PART 3: Innovation in staff sourcing, training and retention - what works and what doesn’t?</itunes:title>
    <title>Where will tomorrow’s workforce come from? PART 3: Innovation in staff sourcing, training and retention - what works and what doesn’t?</title>
    <itunes:summary><![CDATA[PART 3: Innovation in staff sourcing, training and retention - what works and what doesn’t?   Welcome to a 4-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment: “Where will tomorrow’s workforce come from?” The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade now, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase in activity from b...]]></itunes:summary>
    <description><![CDATA[<p><b>PART 3: Innovation in staff sourcing, training and retention - what works and what doesn’t? </b><br/><br/>Welcome to a 4-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment: “Where will tomorrow’s workforce come from?”</p><p>The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade now, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase in activity from both investors and big pharma. But with this relentless pace of growth and innovation comes the fundamental challenge of developing a sufficiently large and skilled workforce to support and maintain the sector. </p><p>In episode 2, we looked predominantly at how the educational system is evolving to meet the specific training and skills requirements of the burgeoning advanced therapies field. In this third episode, we turn the spotlight onto the cell and gene therapy industry and how it is approaching staff development and retention – a crucial area that has been made all the more challenging by the current high level of competition for talent in the field, as well as the evolving mindset of workers relating to their career development and pathway that has been wrought by the Covid-19 pandemic, amongst other things. </p><p>So what are the keys to ensuring a cell or gene therapy company can keep hold of its brightest stars and help them to flourish and grow? Hear the thoughts of <b>Sven Kili, James Miskin, Michael Lehmicke, Qasim Rafiq and Emily Hopewell.</b></p>]]></description>
    <content:encoded><![CDATA[<p><b>PART 3: Innovation in staff sourcing, training and retention - what works and what doesn’t? </b><br/><br/>Welcome to a 4-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment: “Where will tomorrow’s workforce come from?”</p><p>The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade now, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase in activity from both investors and big pharma. But with this relentless pace of growth and innovation comes the fundamental challenge of developing a sufficiently large and skilled workforce to support and maintain the sector. </p><p>In episode 2, we looked predominantly at how the educational system is evolving to meet the specific training and skills requirements of the burgeoning advanced therapies field. In this third episode, we turn the spotlight onto the cell and gene therapy industry and how it is approaching staff development and retention – a crucial area that has been made all the more challenging by the current high level of competition for talent in the field, as well as the evolving mindset of workers relating to their career development and pathway that has been wrought by the Covid-19 pandemic, amongst other things. </p><p>So what are the keys to ensuring a cell or gene therapy company can keep hold of its brightest stars and help them to flourish and grow? Hear the thoughts of <b>Sven Kili, James Miskin, Michael Lehmicke, Qasim Rafiq and Emily Hopewell.</b></p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/10825855-where-will-tomorrow-s-workforce-come-from-part-3-innovation-in-staff-sourcing-training-and-retention-what-works-and-what-doesn-t.mp3" length="18780301" type="audio/mpeg" />
    <itunes:image href="https://storage.buzzsprout.com/uacq453kdw1ry5kb8qp82snl8qzn?.jpg" />
    <itunes:author>Sven Kili, James Miskin, Michael Lehmicke, Qasim Rafiq and Emily Hopewell</itunes:author>
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    <pubDate>Mon, 20 Jun 2022 21:00:00 +0000</pubDate>
    <itunes:duration>1561</itunes:duration>
    <itunes:keywords></itunes:keywords>
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    <itunes:title>Where will tomorrow’s workforce come from? PART 2: How is the educational system responding, and how can the cell and gene therapy community at large help?</itunes:title>
    <title>Where will tomorrow’s workforce come from? PART 2: How is the educational system responding, and how can the cell and gene therapy community at large help?</title>
    <itunes:summary><![CDATA[Part 2: How is the educational system responding, and how can the cell and gene therapy community at large help? Welcome to a four-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment: “Where will tomorrow’s workforce come from?” The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase ...]]></itunes:summary>
    <description><![CDATA[<p><b>Part 2: How is the educational system responding, and how can the cell and gene therapy community at large help?<br/></b>Welcome to a four-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment: “Where will tomorrow’s workforce come from?” The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase in activity from both investors and big pharma. But with this relentless pace of growth and innovation comes the fundamental challenge of developing a sufficiently large and skilled workforce to support and maintain the sector. In this second episode, we look at some of the ways in which the academic and industry communities are responding today, as well as important focus areas for future initiatives, with <b>Sven Kili</b>, <b>James Miskin</b>, <b>Michael Lehmicke</b>, <b>Qasim Rafiq</b>, <b>Emily Hopewell</b>, <b>Frank Barry</b> and <b>Parviz Shamlou</b>.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Part 2: How is the educational system responding, and how can the cell and gene therapy community at large help?<br/></b>Welcome to a four-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment: “Where will tomorrow’s workforce come from?” The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase in activity from both investors and big pharma. But with this relentless pace of growth and innovation comes the fundamental challenge of developing a sufficiently large and skilled workforce to support and maintain the sector. In this second episode, we look at some of the ways in which the academic and industry communities are responding today, as well as important focus areas for future initiatives, with <b>Sven Kili</b>, <b>James Miskin</b>, <b>Michael Lehmicke</b>, <b>Qasim Rafiq</b>, <b>Emily Hopewell</b>, <b>Frank Barry</b> and <b>Parviz Shamlou</b>.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/10751235-where-will-tomorrow-s-workforce-come-from-part-2-how-is-the-educational-system-responding-and-how-can-the-cell-and-gene-therapy-community-at-large-help.mp3" length="23457680" type="audio/mpeg" />
    <itunes:image href="https://storage.buzzsprout.com/jsnimon910tuml5ybn16q6ljtkye?.jpg" />
    <itunes:author>Sven Kili, James Miskin, Michael Lehmicke, Qasim Rafiq, Emily Hopewell, Frank Barry and Parviz Shamlou</itunes:author>
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    <pubDate>Tue, 07 Jun 2022 12:00:00 +0000</pubDate>
    <itunes:duration>1950</itunes:duration>
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    <itunes:title>Where will tomorrow’s workforce come from? PART1: Framing the issue</itunes:title>
    <title>Where will tomorrow’s workforce come from? PART1: Framing the issue</title>
    <itunes:summary><![CDATA[Welcome to a 4-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment:  “Where will tomorrow’s workforce come from?”  The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase in activity from both investors and big pharma. But with this relentless pace of growth and innovation comes the f...]]></itunes:summary>
    <description><![CDATA[<p>Welcome to a 4-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment: <br/><b>“Where will tomorrow’s workforce come from?”<br/></b><br/>The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase in activity from both investors and big pharma. But with this relentless pace of growth and innovation comes the fundamental challenge of developing a sufficiently large and skilled workforce to support and maintain the sector.<br/><br/>In this first episode of the series, we will frame the scale and nature of the issue through the eyes of cell and gene therapy leaders including <b>Sven Kili</b>, <b>James Miskin</b>, <b>Michael Lehmicke</b>, <b>Qasim Rafiq</b>, <b>Emily Hopewell</b>, <b>Frank Barry</b> and <b>Parviz Shamlou</b>.</p>]]></description>
    <content:encoded><![CDATA[<p>Welcome to a 4-part series exploring a question that the entire cell and gene therapy community is struggling with at the moment: <br/><b>“Where will tomorrow’s workforce come from?”<br/></b><br/>The cell and gene therapy field has been advancing at a breakneck speed for the best part of a decade, fuelled by long-awaited clinical successes, commercial breakthroughs, and a related startling increase in activity from both investors and big pharma. But with this relentless pace of growth and innovation comes the fundamental challenge of developing a sufficiently large and skilled workforce to support and maintain the sector.<br/><br/>In this first episode of the series, we will frame the scale and nature of the issue through the eyes of cell and gene therapy leaders including <b>Sven Kili</b>, <b>James Miskin</b>, <b>Michael Lehmicke</b>, <b>Qasim Rafiq</b>, <b>Emily Hopewell</b>, <b>Frank Barry</b> and <b>Parviz Shamlou</b>.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/10750924-where-will-tomorrow-s-workforce-come-from-part1-framing-the-issue.mp3" length="20752858" type="audio/mpeg" />
    <itunes:image href="https://storage.buzzsprout.com/s8ecco0niddhqna5k8w3hhvae0aa?.jpg" />
    <itunes:author>Sven Kili, James Miskin, Michael Lehmicke, Qasim Rafiq, Emily Hopewell, Frank Barry and Parviz Shamlou</itunes:author>
    <guid isPermaLink="false">Buzzsprout-10750924</guid>
    <pubDate>Tue, 07 Jun 2022 10:00:00 +0000</pubDate>
    <itunes:duration>1725</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>4</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
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  <item>
    <itunes:title>The quest for the Holy Grail in AAV chromatography: empty–full separation</itunes:title>
    <title>The quest for the Holy Grail in AAV chromatography: empty–full separation</title>
    <itunes:summary><![CDATA[Ratish Krishnan and Oliver Rammo share their thoughts on the need for a more nuanced understanding of AAV capture and empty–full separation, and the trends driving innovation in this area. ]]></itunes:summary>
    <description><![CDATA[<p><b>Ratish Krishnan</b> and <b>Oliver Rammo</b> share their thoughts on the need for a more nuanced understanding of AAV capture and empty–full separation, and the trends driving innovation in this area.</p>]]></description>
    <content:encoded><![CDATA[<p><b>Ratish Krishnan</b> and <b>Oliver Rammo</b> share their thoughts on the need for a more nuanced understanding of AAV capture and empty–full separation, and the trends driving innovation in this area.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/10680219-the-quest-for-the-holy-grail-in-aav-chromatography-empty-full-separation.mp3" length="14391513" type="audio/mpeg" />
    <itunes:author>Ratish Krishnan &amp; Oliver Rammo</itunes:author>
    <guid isPermaLink="false">Buzzsprout-10680219</guid>
    <pubDate>Wed, 25 May 2022 14:00:00 +0000</pubDate>
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    <psc:chapters>
  <psc:chapter start="0:00" title="The quest for the Holy Grail in AAV chromatography: empty–full separation" />
  <psc:chapter start="1:06" title="Q1: What are the challenges in AAV empty–full separation?" />
  <psc:chapter start="5:23" title="Q2: How well understood is empty–full capsid separation in the gene therapy industry? What are some of the misconceptions?" />
  <psc:chapter start="8:09" title="Q3: Olli, how is Merck tackling the AAV capture and empty–full separation challenge?" />
  <psc:chapter start="11:41" title="Q4: How can analytics drive innovation in this area?" />
  <psc:chapter start="14:52" title="Q5: Looking to the future, how do you expect to see technology for AAV capture and empty–full separation evolve over the next 5 years?" />
  <psc:chapter start="16:59" title="Q6: How will future trends in AAV capsid design and production affect purification?" />
</psc:chapters>
    <itunes:duration>1196</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>3</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
  </item>
  <item>
    <itunes:title>Residual DNA testing in viral vector manufacture: exploring the challenges and solutions</itunes:title>
    <title>Residual DNA testing in viral vector manufacture: exploring the challenges and solutions</title>
    <itunes:summary><![CDATA[In this episode Ilaria Scarfone Field Application Specialist, Pharma Analytics, Thermo Fisher Scientific speaks to Mike Brewer, Director and Global Principal Consultant, BioProduction Division, Thermo Fisher Scientific about the challenges for residual DNA testing in viral vector manufacture.  To read this interview and access lots more content, visit the Cell and Gene Therapy Insights website. ]]></itunes:summary>
    <description><![CDATA[<p>In this episode <b>Ilaria Scarfone </b>Field Application Specialist, Pharma Analytics, Thermo Fisher Scientific <b>speaks to</b> <b>Mike Brewer,</b> Director and Global Principal Consultant, BioProduction Division, Thermo Fisher Scientific about the challenges for residual DNA testing in viral vector manufacture.<br/><br/><a href='https://insights.bio/cell-and-gene-therapy-insights/journal/article/2362/Residual-DNA-testing-in-viral-vector-manufacture-exploring-the-challenges-and-solutions'>To read this interview</a> and access lots more content, visit the <em>Cell and Gene Therapy Insights</em> website.</p>]]></description>
    <content:encoded><![CDATA[<p>In this episode <b>Ilaria Scarfone </b>Field Application Specialist, Pharma Analytics, Thermo Fisher Scientific <b>speaks to</b> <b>Mike Brewer,</b> Director and Global Principal Consultant, BioProduction Division, Thermo Fisher Scientific about the challenges for residual DNA testing in viral vector manufacture.<br/><br/><a href='https://insights.bio/cell-and-gene-therapy-insights/journal/article/2362/Residual-DNA-testing-in-viral-vector-manufacture-exploring-the-challenges-and-solutions'>To read this interview</a> and access lots more content, visit the <em>Cell and Gene Therapy Insights</em> website.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/10645417-residual-dna-testing-in-viral-vector-manufacture-exploring-the-challenges-and-solutions.mp3" length="11918151" type="audio/mpeg" />
    <link>https://insights.bio/cell-and-gene-therapy-insights/journal/article/2362/Residual-DNA-testing-in-viral-vector-manufacture-exploring-the-challenges-and-solutions</link>
    <itunes:author>Ilaria Scarfone and Mike Brewer</itunes:author>
    <guid isPermaLink="false">Buzzsprout-10645417</guid>
    <pubDate>Thu, 19 May 2022 11:00:00 +0000</pubDate>
    <podcast:chapters url="https://www.buzzsprout.com/1986893/10645417/chapters.json" type="application/json" />
    <psc:chapters>
  <psc:chapter start="0:00" title="Residual DNA testing in viral vector manufacture: exploring the challenges and solutions" />
  <psc:chapter start="1:08" title="Q1. Mike, to begin, could you give a brief introduction and background on the residual DNA testing regulatory requirements in general, and why gene therapy products present some particular challenges?" />
  <psc:chapter start="4:43" title="Q2. Before we analyze each of these particular concerns, let’s discuss some of the challenges in the development and validation of residual DNA analytical assays in general, and in particular for gene therapy." />
  <psc:chapter start="8:23" title="Q3. Looking at validation and qualification, how does the Thermo Fisher Scientific development validation study help ensure the quality of the kits, and how does this differ from the validation of the method for regulatory approval?" />
  <psc:chapter start="12:14" title="Q5. Do you have any suggestions on how to address copy number versus mass concerns?" />
  <psc:chapter start="12:17" title="Q4, Focusing on gene therapy, and residual DNA testing in particular, let’s address a couple of specific questions I am often asked by customers. How do we help simplify the process of measuring vector DNA, and how do we address the challenges of fragme" />
</psc:chapters>
    <itunes:duration>990</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>2</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
    <itunes:explicit>false</itunes:explicit>
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  <item>
    <itunes:title>Precisely for CGT: automating aseptic filling for lowest volumes</itunes:title>
    <title>Precisely for CGT: automating aseptic filling for lowest volumes</title>
    <itunes:summary><![CDATA[In this Episode, Roisin McGuigan, Editor at BioInsights, speaks to Dr Barbara Fisher, Process Consultant at Single Use Support about automating aseptic filling for lowest volumes. Barbara works with both established pharmaceutical manufacturers and start-up companies, and has in-depth expedience in low bioburden and aseptic GMP manufacturing from downstream processing to fill and finish.   To read this interview and access lots more content, visit the Cell and Gene Therapy Insights websi...]]></itunes:summary>
    <description><![CDATA[<p>In this Episode, Roisin McGuigan, Editor at BioInsights, speaks to Dr Barbara Fisher, Process Consultant at Single Use Support about automating aseptic filling for lowest volumes. Barbara works with both established pharmaceutical manufacturers and start-up companies, and has in-depth expedience in low bioburden and aseptic GMP manufacturing from downstream processing to fill and finish. <br/><br/><a href='https://insights.bio/cell-and-gene-therapy-insights/journal/article/2420/Precisely-for-CGT-automating-aseptic-filling-for-lowest-volumes'>To read this interview</a> and access lots more content, visit the <em>Cell and Gene Therapy Insights</em> website.</p>]]></description>
    <content:encoded><![CDATA[<p>In this Episode, Roisin McGuigan, Editor at BioInsights, speaks to Dr Barbara Fisher, Process Consultant at Single Use Support about automating aseptic filling for lowest volumes. Barbara works with both established pharmaceutical manufacturers and start-up companies, and has in-depth expedience in low bioburden and aseptic GMP manufacturing from downstream processing to fill and finish. <br/><br/><a href='https://insights.bio/cell-and-gene-therapy-insights/journal/article/2420/Precisely-for-CGT-automating-aseptic-filling-for-lowest-volumes'>To read this interview</a> and access lots more content, visit the <em>Cell and Gene Therapy Insights</em> website.</p>]]></content:encoded>
    <enclosure url="https://www.buzzsprout.com/1986893/episodes/10592334-precisely-for-cgt-automating-aseptic-filling-for-lowest-volumes.mp3" length="10978061" type="audio/mpeg" />
    <itunes:author>BioInsights</itunes:author>
    <guid isPermaLink="false">Buzzsprout-10592334</guid>
    <pubDate>Tue, 10 May 2022 13:00:00 +0000</pubDate>
    <podcast:soundbite startTime="25.0" duration="15.0" />
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    <psc:chapters>
  <psc:chapter start="0:00" title="Precisely for CGT: automating aseptic filling for lowest volumes" />
  <psc:chapter start="0:59" title="Q1. What are the most important factors to consider when looking to make significant cost savings?" />
  <psc:chapter start="3:04" title="Q2. What are the biggest hurdles that need to be overcome to address the issues of standardization and scale-up, and speed up this process?" />
  <psc:chapter start="6:28" title="Q3. What specific trends are you seeing currently in the selection of primary packaging?" />
  <psc:chapter start="10:18" title="Q4. What are the key challenges and limitations when using single-use bags in small volume manufacturing?" />
  <psc:chapter start="13:10" title="Q5. What are your top recommendations for manufacturers who are transferring a process from manual to automized production?" />
</psc:chapters>
    <itunes:duration>911</itunes:duration>
    <itunes:keywords></itunes:keywords>
    <itunes:season>1</itunes:season>
    <itunes:episode>1</itunes:episode>
    <itunes:episodeType>full</itunes:episodeType>
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