Overview
Adaptive design in clinical trials is growing in popularity and are increasingly seen as more efficient than trials using traditional fixed designs. This approach provides the flexibility to modify studies with pre-specified rules during the trial, once partial data are collected.
Using real-world examples from the pharmaceutical industry, this virtual course provides a comprehensive review of the concepts and methods underpinning adaptive clinical designs and examines their application in drug development. It will also provide an overview of data monitoring and regulatory guidance relevant to adaptive designs will also be presented.
Have an account?