While clinical registries are a valued source of longitudinal, real-world data, registries also provide expanded options for research and advancing randomized clinical trials. Understanding when and how to use registries in these use cases is quite nuanced and mandates a targeted approach and innovative expertise. In this video, we dive deep into the expanded use of registries as external control arms in clinical trials.
Watch this video and learn more:
Challenges faced by biopharma companies conducting clinical trials when studying rare conditions.
The purpose of a control population in traditional randomized controlled clinical trials.
How hybrid control arms can improve the strength of control groups.
How prospective registries serve as real-world control populations.
How to minimize bias between populations or outcome measures across RCT control groups vs. real-world/hybrid controls.