Pooling Different Placebos as a Control Group in a Randomized Platform Trial: Benefits and Challenges From Experience in the ACTIV-2 COVID-19 Trial

Author:

Moser Carlee B1ORCID,Chew Kara W2,Ritz Justin1,Newell Matthew3,Javan Arzhang Cyrus4,Eron Joseph J3,Daar Eric S5,Wohl David A3ORCID,Currier Judith S2ORCID,Smith Davey M6,Hughes Michael D7,Hosey Lara,Roa Jhoanna,Patel Nilam,Aldrovandi Grace,Murtaugh William,Cooper Marlene,Gutzman Howard,Knowles Kevin,Bowman Rachel,Giganti Mark,Erhardt Bill,Adams Stacey,

Affiliation:

1. Center for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health , Boston, Massachusetts , USA

2. Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles,   Los Angeles, California , USA

3. Department of Medicine, University of North Carolina at Chapel Hill School of Medicine , Chapel Hill, North Carolina , USA

4. Division of AIDS/National Institute of Allergy and Infectious Diseases, National Institutes of Health , Rockville, Maryland , USA

5. Lundquist Institute at Harbor-UCLA Medical Center , Torrance, California , USA

6. Department of Medicine, University of California, San Diego , La Jolla, California , USA

7. Department of Biostatistics and Center for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health , Boston, Massachusetts , USA

Abstract

Abstract Adaptive platform trials were implemented during the coronavirus disease 2019 (COVID-19) pandemic to rapidly evaluate therapeutics, including the placebo-controlled phase 2/3 ACTIV-2 trial, which studied 7 investigational agents with diverse routes of administration. For each agent, safety and efficacy outcomes were compared to a pooled placebo control group, which included participants who received a placebo for that agent or for other agents in concurrent evaluation. A 2-step randomization framework was implemented to facilitate this. Over the study duration, the pooled placebo design achieved a reduction in sample size of 6% versus a trial involving distinct placebo control groups for evaluating each agent. However, a 26% reduction was achieved during the period when multiple agents were in parallel phase 2 evaluation. We discuss some of the complexities implementing the pooled placebo design versus a design involving nonoverlapping control groups, with the aim of informing the design of future platform trials. Clinical Trials Registration. NCT04518410.

Funder

National Institute of Allergy and Infectious Diseases

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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