Designing a Phase I or II clinical trial requires decisions about endpoints, dose, safety, and what can be learned from a small study. Join the NIH Library for a new two-part online series that explores these decisions through biostatistical methods, practical examples, and case studies. Start with the foundations of early-phase trial design, then consider how approaches developed in oncology can inform trials in other disease areas. View class links for details and to register.
Part 1: Early-Phase Clinical Trials Design: Introduction
November 2, 11:00 am – 12:30 pm
Learn how choices about endpoints, dose determination, and study design shape Phase I and II trials. This 90-minute online class is intended for participants with basic knowledge of clinical trials. Instructor: Dr. Xiaobai Li, CC/BCES
Part 2: Early-Phase Clinical Trial Design: Oncology Innovations for Other Disease Areas
November 3, 11:00 am – 12:30 pm
Explore when oncology dose-finding and adaptive design approaches may be useful in other disease areas, especially trials with response-based endpoints. This 90-minute online class is taught by an NCI statistician. Instructor: Dr. Hyoyoung Choo-Wosoba, NCI
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