
FDA has laid out what it will accept to approve a psychedelic therapy: 12-week efficacy data plus preliminary follow-up. On the latest BioCentury This Week podcast, BioCentury's analysts assess what that means for sponsors navigating trial design with the agency. The team also discusses Michael Davis' first interview as permanent CDER director and what it signals for regulatory stability after a turbulent year, plus preclinical advances positioning suppressor tRNAs as a platform for Duchenne,...
Podzilla Summary coming soon
Sign up to get notified when the full AI-powered summary is ready.
Free forever for up to 3 podcasts. No credit card required.

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

Ep. 385 - MFN deals, Lilly takeout, FDA pick Overton

Ep. 384 - Back to School Special: The global FIH trials race

Ep. 383 - Moderna, Genentech obesity deal, Trump's FDA pick
Free AI-powered recaps of BioCentury This Week and your other favorite podcasts, delivered to your inbox.
Free forever for up to 3 podcasts. No credit card required.