Designing precision medicine trials to yield a greater population impact.

ABSTRACT: Traditionally, a clinical trial is conducted comparing treatment to standard care for all patients. However, it could be inefficient given patients' heterogeneous responses to treatments, and rapid advances in the molecular understanding of diseases have made biomarker-based clinical trials increasingly popular. We propose a new targeted clinical trial design, termed as Max-Impact design, which selects the appropriate subpopulation for a clinical trial and aims to optimize population impact once the trial is completed. The proposed design not only gains insights on the patients who would be included in the trial but also considers the benefit to the excluded patients. We develop novel algorithms to construct enrollment rules for optimizing population impact, which are fairly general and ca

SUBMITTER: Zhao YQ 

PROVIDER: S-EPMC7211185 | biostudies-literature | 2020 Jun

REPOSITORIES: biostudies-literature