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BioCentury This Week

BioCentury
BioCentury This Week
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400 episodes

  • BioCentury This Week

    Ep. 390 - Live from Amsterdam: Grand Rounds Europe takeaways

    30/09/2026 | 34 mins.
    Mechanisms broad enough to matter across many diseases, from mitochondrial health to the biology of aging, emerged as a defining theme at Grand Rounds Europe in Amsterdam. On a special live edition of the BioCentury This Week podcast, BioGeneration Ventures' Oskar Slotboom, NautaDutilh's Ruud Smits and Leyden Labs' Dinko Valerio join BioCentury's analysts to discuss women's health and sleep as lenses on disease, and the shift toward prevention.
    The panel also weighs the limits of "Frankenstein" multiparatopic molecules and AI-driven discovery, knowledge gaps in autonomous labs, new China first-in-human rules, and what Novartis' Lp(a) miss means for genetically validated targets.

    View full story: https://www.biocentury.com/article/660970

    #EuropeBiotech #DrugDiscovery #TranslationalMedicine #GeneticTargets #HealthSpan

    0:00 Introduction
    2:10 Bridging Academia & Industry
    14:51 Key Themes
    26:02 Toolbox and Biology
    31:05 Lp(a) Fallout & Genetic Targets

    To submit a question to BioCentury’s editors, email the BioCentury This Week team at podcasts@biocentury.com.
    Reach us by sending a text
  • BioCentury This Week

    Ep. 389 - IgA nephropathy, Overton hearing, reverse mergers' new look

    29/09/2026 | 37 mins.
    Seven global approvals in five years, validated biomarkers and FDA flexibility have turned IgA nephropathy from a neglected rare disease into a crowded field, with Biogen, Novartis, Takeda, Climb Bio and Jade chasing targets such as APRIL, BAFF and CD38. On the latest BioCentury This Week podcast, BioCentury's analysts assess how next-generation therapies are competing on safety and longer dosing intervals.
    The analysts also discuss Heidi Overton's FDA commissioner confirmation hearing and lingering questions about her independence, new pharma tariff guidance that leaves exemptions unclear, and how reverse mergers paired with nine-figure PIPEs became a viable IPO alternative. Plus, Merck's $400 million upfront bet on a preclinical KRAS G12C molecular glue.

    View full story: https://www.biocentury.com/article/660935

    #IgANephropathy #FDA #BiotechIPO #DrugDevelopment #ClinicalTrials

    0:00 Introduction
    1:30 Grand Rounds: Europe Recap
    6:03 IgA Nephropathy Pipeline
    14:57 Overton Hearing
    22:19 Commerce's Tariff Guidance
    24:28 Reverse Mergers' New Look

    To submit a question to BioCentury’s editors, email the BioCentury This Week team at podcasts@biocentury.com.
    Reach us by sending a text
  • BioCentury This Week

    Ep. 388 - Biotech IPOs, CAR T safety & pharma tariffs

    22/09/2026 | 32 mins.
    The first biotech IPO in a month, Electra's upsized $350 million offering, fell in its trading debut, testing investor appetite while a wave of reverse mergers showcases an alternate route to NASDAQ. On the latest BioCentury This Week podcast, BioCentury's analysts examine momentum in the biotech IPO market.
    The team also unpacks fatal toxicities in Novartis' autoimmune CAR-T trials and what they reveal about manufacturing, dosing and immune biology risks across the modality. In Washington, Steve Usdin previews Heidi Overton's FDA Commissioner confirmation hearing and reports on the persistent uncertainty around pharma tariffs ahead of the Sept. 29 deadline.

    View full story: https://www.biocentury.com/article/660870

    #BiotechIPO #CARTCell #FDA #PharmaTariffs #DrugDevelopment

    0:00 Introduction
    02:15 Biotech IPO Market
    10:38 Autoimmune CAR-T Safety
    21:56 FDA Commissioner Hearing
    26:47 Pharma Tariff Uncertainty

    To submit a question to BioCentury’s editors, email the BioCentury This Week team at podcasts@biocentury.com.
    Reach us by sending a text
  • BioCentury This Week

    Ep. 387 - Psychedelics at FDA, Mike Davis’ CDER & tRNAs

    15/09/2026 | 30 mins.
    Note: This episode was briefly published with an incorrect audio file, which has since been corrected.

    FDA is prepared to approve psychedelic therapies for chronic psychiatric disorders before sponsors have fully determined how long the effects last or when patients should receive second or subsequent doses. On the latest BioCentury This Week podcast, BioCentury's analysts assess the latest guidance on psychedelics from FDA.
    The team also discusses takeaways from Michael Davis' first interview as CDER director, plus preclinical advances positioning suppressor tRNA for Duchenne, cystic fibrosis, and other nonsense-mutation diseases. They also highlight Emerging Company Profiles on BrainChild and Cloverleaf.

    View full story: https://www.biocentury.com/article/660792

    #Psychedelics #FDA #GeneTherapy #ClinicalTrials #DrugDevelopment

    0:00 - Introduction
    1:13 - Psychedelics at FDA
    10:20 - Mike Davis Leads CDER
    22:29 - Suppressor tRNAs Advance

    To submit a question to BioCentury’s editors, email the BioCentury This Week team at podcasts@biocentury.com.
    Reach us by sending a text
  • BioCentury This Week

    Ep. 386 - Novartis misses, pharma deals analysis, MFN carve-outs

    09/09/2026 | 35 mins.
    A pair of high profile clinical setbacks has wiped out more than $40 billion in market cap for Novartis, most of which stemmed from the Phase III miss of antisense oligonucleotide therapy pelacarsen. On the latest BioCentury This Week podcast, BioCentury's analysts unpack the fallout for Lp(a) as a cardio target and whether issues with the target, modality or treatment setting contributed to the therapy's lack of efficacy. The analysts also review BioCentury's annual big pharma deals analysis, which found industry's largest players leaning into disruptive platforms such as bispecifics, in vivo CAR Ts, siRNAs, and degraders. In Washington, Steve Usdin reports on most-favored nation drug pricing carve-outs and policy pressure on mid-tier biotechs – plus the conspicuous lack of U.S. biotechs coming to the table -- pays tribute to the late Peter Barton Hutt, the former FDA Chief Counsel who shaped foundational elements of modern FDA law.

    View full story: https://www.biocentury.com/article/660746

    #CardiovascularDisease #DrugPricing #BiotechMA #ClinicalTrials #FDA 

    0:00 - Introduction 
    1:23 - Novartis Phase III Fallout
    18:24 - Annual Pharma Deals Analysis
    27:42 - MFN Carve-Outs
    32:39 - Remembering Peter Barton Hutt

    To submit a question to BioCentury’s editors, email the BioCentury This Week team at podcasts@biocentury.com.
    Reach us by sending a text
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About BioCentury This Week
BioCentury's streaming commentary on biotech industry trends, plus interviews with KOLs.For three decades, BioCentury has helped biopharma executives and investors make business-critical decisions and build larger networks with peers across the innovation ecosystem.
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