Volker Herrmann is the President and CEO of Sonata Therapeutics, a Flagship Pioneering company revolutionizing the world’s understanding of the cellular microenvironment and its importance to human biology and disease. Sonata’s product-platform creates drugs based on a systematic, comprehensive characterization of the microenvironment in diseases with high unmet medical need. Volker discusses the arc of his career, starting with attending medical school in Germany, then training as a cardiologist and clinical pharmacologist before working at Pfizer. He talks about his transition from big pharma to biotech and how his approach to running a biotech has evolved. He discusses the importance of patient impact and how that drives him in this industry. He talks about their work at Sonata to develop therapeutics for cancer and other diseases, and how he thinks about indication selection.

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Greg Flesher is the President and CEO of Reneo Pharmaceuticals, a clinical-stage pharmaceutical company focused on the development of therapies for patients with rare genetic mitochondrial diseases with significant unmet medical needs. Greg discusses beginning his career at Eli Lilly in the mid-1990s and how he approaches being a CEO differently the second time around. He talks about the rare mitochondrial disease landscape and the opportunities and challenges within it. He also dives into patient access for rare diseases and the difficulties around accessing the right patients for late-stage pivotal trials. Finally, he shares how the current environment impacts how he approaches execution against clinical programs and his advice to other leaders navigating the current times.

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Adrian Gottschalk is the president and CEO of Foghorn Therapeutics, a clinical-stage biotechnology company pioneering a new class of medicines that treat cancers and other serious diseases by correcting abnormal gene expression. Adrian discusses his early beginnings at Biogen before joining Foghorn. He talks about the evolution of his role as CEO at Foghorn, particularly as the company has grown tremendously from a small biotech to a clinical-stage company. He discusses the work his team is pursuing at Foghorn, the overall landscape for therapeutic options in oncology, and what’s changed with our ability to modulate gene expression. He also dives into Foghorn’s pipeline of over 15 different programs and its two major collaborations with Merck and Loxo Lilly Oncology.

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Jim Brown is the President and CEO of DURECT Corporation, a biopharmaceutical company committed to transforming the treatment of acute organ injuries and chronic liver diseases by advancing novel and potentially lifesaving epigenetic therapies. Jim discusses how his early beginnings as a vet ultimately led him to the biotech industry. He talks about epigenetic regulation and how it ties into the work DURECT is leading. He dives into the unmet need for treatment of liver diseases such as alcohol-associated hepatitis and how he gets capital markets to understand the potential impact in an area where there isn’t a lot of awareness. He also discusses where the company is from a development perspective, their plans to commercialize, and his advice to other entrepreneurs and leaders as they navigate the inherent risk that’s involved in developing a new therapeutic.

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James Peyer, Ph.D., is the Founder and CEO of Cambrian Bio, a clinical-stage biopharmaceutical company focused on developing therapies to prevent and cure age-related diseases. James discusses the driving force behind his interest in aging biology and oncology, how his perspective on aging has changed over the years, and what he hopes to achieve over the next decade. He talks about his entrepreneurial journey and fundraising experience. He also discusses the inherent risk involved in drug development, how he manages the emotional aspects of that, and Cambrian’s unique approach to drug development.

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Gary Lee, Ph.D. is the CSO of Lyell Immunopharma, a T-cell reprogramming company dedicated to developing cell therapies for patients with solid tumors. A chemical engineer by training, Gary has been working in the gene therapy field for 20+ years. He discusses how he’s observed the cell therapy space evolve over the last couple of decades. He talks about the work his team is doing to develop effective cell-based therapies for solid tumor cancers and where they are from a development and team-building perspective. He also provides his perspective on opportunities he sees for future technology across the cell therapy landscape.

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Liang Schweizer, Ph.D. is the Founder and CEO of HiFiBiO Therapeutics, a clinical-stage global biotech company mobilizing the human immune system to combat disease. The company integrates deep-rooted biological expertise with comprehensive single-cell profiling technologies to rapidly discover and advance a pipeline of antibody drugs to treat cancer and autoimmune disorders. Liang shares her perspective on the Chinese biotech ecosystem and how it has evolved over the last couple of years. She also discusses how approaches to drug development have changed, specifically around leveraging technology and the intersection of science and technology. She talks about being a CEO for the first time and how she approaches managing globally distributed teams.

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Detlev Biniszkiewicz is the Founder and CEO of NextPoint Therapeutics, a company advancing the field of immuno-oncology through its leading scientific work on the novel HHLA2 pathway. Detlev discusses the immuno-oncology landscape including its challenges and opportunities, and the work his team is pursuing at NextPoint to deliver new therapies to cancer patients. He talks about how he operates and leads as a CEO and how he approaches team building. He also shares his advice to others that are in an early stage company, and discusses the current macro environment across biotech.

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Eric Dobmeier is the President and CEO of Chinook Therapeutics, a clinical-stage biopharmaceutical company discovering, developing and commercializing precision medicines for rare, severe chronic kidney diseases. Eric discusses how his early years as a lawyer working in-house as general counsel for Seattle Genetics (now Seagen), ultimately led him to running his own biotech company. He talks about the landscape of kidney disease, the current unmet need, what opportunities he sees in the space, and the growing interest in kidney disease amongst big pharma. He also discusses the progress Chinook has made over the last several years, particularly the three clinical stage programs they currently have, and what’s ahead for the company.

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Faraz Ali is the CEO of Tenaya Therapeutics, a clinical-stage biotechnology company with a mission to discover, develop and deliver potentially curative therapies that address the underlying causes of heart disease. Faraz discusses his non-traditional background as an electrical engineer before he found his passion for applying science and technology to healthcare problems. He talks about his experience working at Genzyme and what aspects from his time there he still carries with him today. Faraz also discusses his perspective on the application of genetic modalities, and his team’s work pursuing treatment for both rare and prevalent forms of heart disease. Finally, he talks about what it’s like being a first time CEO and his thoughts on team building.

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Gregory Verdine, Ph.D., is the Co-Founder, President and CEO of LifeMine Therapeutics and FogPharma. LifeMine Therapeutics is reinventing drug discovery by mining genetically-encoded small molecules (GEMs) from the biosphere. FogPharma is developing a new class of drugs to address the limitations of today’s precision medicines and achieve universal druggability. In this episode, Greg discusses his unique journey from starting as an academic scientist to transitioning to an investor, and how that exposure to the venture world rounds out his approach to how he now runs biotechs. He talks about what it’s been like running two companies for six years and how he structures his time so he can successfully operate between the two. He also discusses fundraising in a challenging environment and the importance of being part of a team in biotech.

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Kate Haviland is the CEO of Blueprint Medicines, a global precision therapy company that creates life-changing medicines for people with cancer and blood disorders. Applying an approach that is both precise and agile, they create medicines that selectively target genetic drivers, with the goal of staying one step ahead across stages of disease. Kate discusses beginning her career at Genzyme before joining Blueprint Medicines, and what the transition to becoming CEO was like after having held various different roles at Blueprint. She also talks about how personalized medicine is transforming patient care, and the company’s focus on applying precision medicine to cancer and hematologic diseases. Finally, she dives into how the current environment informs how she approaches leading a publicly traded biotech and her perspective on partnerships.

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