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August 4, 2025
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Episode 23, “Bayesian Approach in Clinical Trials”

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This episode of "In the Interim…" features Dr. Scott Berry, Dr. Kert Viele, and Dr. Melanie Quintana of Berry Consultants dissecting the technical and operational landscape of Bayesian statistics in clinical trial design.

Episode 23 of “In the Interim…” features Dr. Scott Berry, Dr. Melanie Quintana, and Dr. Kert Viele for an analytical discussion on the actual impact of Bayesian statistics in clinical trials.

Highlights include REBYOTA’s FDA approval—where only posterior probabilities appear on the FDA label from prospectively combined analyses of Phase 2 and Phase 3 data—and how ALS and rare disease platform trials use dynamic borrowing across subgroups and endpoints. Bayesian approaches are reframing evidentiary requirements, now referenced by FDA and EMA guidance.

Interested in hearing about Bayesian approaches by three professed Bayesians in the clinical trial arena?

Listen to the full episode today: https://www.berryconsultants.com/resource/23-bayesian-approach-in-clinical-trials

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