As part of our 2025 Simulation Guided Trial Design series, in this webinar Tom Parke designs a classic Phase I trial using i3+3, BOIN, m-TPI-2 methods or CRM (Continuous Re-assessment Method using Bayesian logistic regression).

In this first webinar of our 2025 Simulation Guided Trial Design series, Scott Berry covers the background and importance of simulations in clinical trial designs.

In this episode of "In the Interim…", Dr. Scott Berry delivers a metaphoric critique of single-question trial infrastructure through the sports arena analogy, illustrating the cost, patient burden, and data inefficiency of conventional clinical trials.

Seamless adaptive trials can deliver higher statistical power with fewer patients and shorter timelines, yet practical funding hurdles persist. Objective administrative (financial) analyses—often Bayesian-driven—can define funding triggers without compromising trial integrity.

In episode 40 of "In the Interim…", Dr. Scott Berry examines the statistical, operational, and behavioral challenges of using interim analyses as triggers for funding in adaptive and seamless Phase II/III clinical trials.

In this episode of "In the Interim...", Dr. Scott Berry interviews Dr. Kaspar Rufibach, Co-Head of Advanced Biostatistical Sciences at Merck.