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The Long Run with Luke Timmerman

Ep201: Jeremy Levin on Biotech in the Balance

68 min episode · 3 min read
·
Jeremy Levin

Episode

68 min

Read time

3 min

Topics

Investing, Startups, Leadership

AI-Generated Summary

Key Takeaways

  • Public identity crisis: Biotech's failure to distinguish itself from pharma created a political vulnerability. Because 70% of new drugs originate in biotech, yet the public conflates the two sectors, every pharma pricing scandal damages small innovative companies. Levin argues each biotech company should actively and publicly separate its identity from pharma—especially when incidents like Shkreli's generic drug price gouging have zero connection to drug invention.
  • China's five-stage biotech strategy: China executed a deliberate 25-year plan: first mastering API chemical manufacturing, then building pharma services, then attracting overseas talent, then producing biosimilars, and now targeting novel drug discovery by 2035. Levin warns that by 2035 China could dominate novel drug output and leverage medicines as a trade weapon—exactly as it has done with batteries, solar panels, and rare earth minerals.
  • FDA leadership turnover as systemic risk: Roughly 90% of FDA leadership changed within approximately one year under current conditions, creating regulatory unpredictability that Levin estimates will take three to ten years to stabilize regardless of which administration follows. Companies and investors should model extended timelines for regulatory approvals and factor in structural uncertainty when planning capital raises and development milestones.
  • Long-term capital reform levers: Levin proposes tiered capital gains taxation—lower rates the longer biotech shares are held—and transferable R&D tax credits modeled on real estate depreciation rules. Separately, replacing quarterly SEC reporting with biannual reporting would redirect roughly half the legal and accounting burden toward science and patient outreach, better matching capital market rhythms to biotech's ten-plus-year development cycles.
  • Ten commitments framework: Levin's book structures industry reform around ten actionable commitments: scientific truth adherence, patients as primary beneficiary, ethical trial conduct, radical transparency in results and failures, regulatory integrity, long-term capital formation, manufacturing resilience, immigration openness, strategic government designation of biotech, and proactive public communication. Each commitment targets a specific trust deficit rather than offering cosmetic rebranding.

What It Covers

Jeremy Levin, founder of Ovid Therapeutics and past BIO chairman, outlines why U.S. biotech faces a structural crisis of public distrust—tracing the decline from Martin Shkreli's 2015 price gouging through COVID vaccine backlash—and presents 10 concrete commitments companies can adopt to rebuild credibility and secure the industry's strategic future.

Key Questions Answered

  • Public identity crisis: Biotech's failure to distinguish itself from pharma created a political vulnerability. Because 70% of new drugs originate in biotech, yet the public conflates the two sectors, every pharma pricing scandal damages small innovative companies. Levin argues each biotech company should actively and publicly separate its identity from pharma—especially when incidents like Shkreli's generic drug price gouging have zero connection to drug invention.
  • China's five-stage biotech strategy: China executed a deliberate 25-year plan: first mastering API chemical manufacturing, then building pharma services, then attracting overseas talent, then producing biosimilars, and now targeting novel drug discovery by 2035. Levin warns that by 2035 China could dominate novel drug output and leverage medicines as a trade weapon—exactly as it has done with batteries, solar panels, and rare earth minerals.
  • FDA leadership turnover as systemic risk: Roughly 90% of FDA leadership changed within approximately one year under current conditions, creating regulatory unpredictability that Levin estimates will take three to ten years to stabilize regardless of which administration follows. Companies and investors should model extended timelines for regulatory approvals and factor in structural uncertainty when planning capital raises and development milestones.
  • Long-term capital reform levers: Levin proposes tiered capital gains taxation—lower rates the longer biotech shares are held—and transferable R&D tax credits modeled on real estate depreciation rules. Separately, replacing quarterly SEC reporting with biannual reporting would redirect roughly half the legal and accounting burden toward science and patient outreach, better matching capital market rhythms to biotech's ten-plus-year development cycles.
  • Ten commitments framework: Levin's book structures industry reform around ten actionable commitments: scientific truth adherence, patients as primary beneficiary, ethical trial conduct, radical transparency in results and failures, regulatory integrity, long-term capital formation, manufacturing resilience, immigration openness, strategic government designation of biotech, and proactive public communication. Each commitment targets a specific trust deficit rather than offering cosmetic rebranding.
  • Proactive mass communication strategy: Rather than relying on trade publications or podcasts, Levin argues biotech should fund broad consumer advertising campaigns—comparable in scale to direct-to-consumer drug ads—that explain the industry's role in creating medicines, not selling them. Patient-centered storytelling aired on mainstream television channels, including news and sports programming, could shift public perception faster than any policy lobbying effort currently underway.

Notable Moment

Levin reveals that when he asked roughly 100 biotech CEOs gathered in Greece to contribute essays for a collective book, only six responded—because executives feared retaliation or uncertainty. That near-silence from an entire industry's leadership, despite widespread private anxiety, prompted Levin to write the book alone.

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Episode Transcript

Welcome to The Long Run. This is a podcast for biotech adventurers. I'm your host, Luke Timmerman. Today's guest is Jeremy Levin. Jeremy is the executive chairman and founder of New York based Ovid Therapeutics. He's also a member of the board of the Biotechnology Innovation Organization and is a past chairman. Jeremy reads widely and thinks deeply about many subjects, including how biotechnology can live up to its potential to uplift humanity. I enjoy talking with him about the conditions that create success in the industry and how things might be changed to get biotech back into a more stable place with more public confidence and trust. Jeremy has sharpened his thinking and sought to share some of it in a new book out today called Biotech in the Balance, Saving a Strategic Industry in an Age of Distrust. It's for biotech executives, policy makers, or any curious citizen interested in how we better harness biotechnology for the betterment of the maximum number of people around the world. It's officially released on May 19, and you can check the show notes on Timmerman Report for a link on how to order a copy. One of the things that I like about this book is that it's not just a laundry list of what's wrong. It contains 10 commitments. These are practical suggestions of things companies can do to make for a healthier industry and to create a more stable, thriving industry that really earns more public support. I hope you enjoy this conversation and that it might even serve as a conversation starter in your own circles. Now, a word from the sponsor of the show. AlphaSense is an AI powered market intelligence platform designed to help investors and operators find critical insights faster. Think of it as a search engine for the entire financial and life sciences landscape, aggregating over 500,000,000 documents across company filings, clinical trial registries, FDA documents, earnings calls, expert transcripts, broker research, and industry publications into one unified searchable platform. For those researching biotech, med tech, and the broader life sciences landscape, it's a game changer, purpose built to surface the clinical, regulatory, and commercial insights that matter most. You can use smart summaries to instantly synthesize thousands of pages of trial data, regulatory filings, and KOL commentary, while while channel checks and expert insights help you understand how therapies are actually being adopted in the real world across physicians, payers, and hospital systems, not just how they're all modeled on paper. Instead of spending hours digging through 10 ks's, AlphaSense surfaces the alpha, the specific insights that move the needle in seconds. To experience it firsthand, you can start a free trial at alpha-sense.com/thelongrun. All one word. That's alpha-sense.com/thelongrun. And, bioanalysis should not rely on which scientists at the CRO you get. These are assays, not consulting. Your results should be the same, regardless of who does the work. We love working with our CRO when we get the right PI is a …

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Books

  • by Jeremy Levin

    Levin's book structures industry reform around ten actionable commitments: scientific truth adherence, patients as primary beneficiary, ethical trial conduct, radical transparency in results and failures, regulatory integrity, long-term capital formation, manufacturing resilience, immigration openness, strategic government designation of biotech, and proactive public communication.

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