Two Stage Designs for Phase III Clinical Trials.

Brownian Motion Optimal Design Platform Trial Surrogate Endpoint Two-Stage Design

Journal

medRxiv : the preprint server for health sciences
Titre abrégé: medRxiv
Pays: United States
ID NLM: 101767986

Informations de publication

Date de publication:
31 Jul 2020
Historique:
pubmed: 15 8 2020
medline: 15 8 2020
entrez: 15 8 2020
Statut: epublish

Résumé

Phase III platform trials are increasingly used to evaluate a sequence of treatments for a specific disease. Traditional approaches to structure such trials tend to focus on the sequential questions rather than the performance of the entire enterprise. We consider two-stage trials where an early evaluation is used to determine whether to continue with an individual study. To evaluate performance, we use the ratio of expected wins (RW), that is, the expected number of reported efficacious treatments using a two-stage approach compared to that using standard phase III trials. We approximate the test statistics during the course of a single trial using Brownian Motion and determine the optimal stage 1 time and type I error rate to maximize RW for fixed power. At times, a surrogate or intermediate endpoint may provide a quicker read on potential efficacy than use of the primary endpoint at stage 1. We generalize our approach to the surrogate endpoint setting and show improved performance, provided a good quality and powerful surrogate is available. We apply our methods to the design of a platform trial to evaluate treatments for COVID-19 disease.

Identifiants

pubmed: 32793927
doi: 10.1101/2020.07.29.20164525
pmc: PMC7418751
pii:
doi:

Types de publication

Preprint

Langues

eng

Auteurs

Dean Follmann (D)

Biostatistics Research Branch, National Institute of Allergy and Infectious Diseases, 5601 Fishers Lane, Bethesda MD 20892, U.S.A.

Michael Proschan (M)

Biostatistics Research Branch, National Institute of Allergy and Infectious Diseases, 5601 Fishers Lane, Bethesda MD 20892, U.S.A.

Classifications MeSH