A Population-Based HIV Vaccine Efficacy Trial Design: Statistical Framework and Design Considerations

An HIV vaccine will be a critical tool for ending the epidemic, yet the next vaccine efficacy trial is likely five or more years away as the field focuses on the early-phase evaluation and optimization of vaccines that induce broadly neutralizing antibodies. At the same time, the HIV prevention landscape has evolved substantially, with the discovery of highly effective means of preventing HIV, challenging the identification of HIV prevention trial designs that are ethically sound and scientifically robust. We explore a population-based, individually randomized, proof-of-concept trial design for evaluating the efficacy of a future candidate vaccine to prevent HIV acquisition and to validate the neutralizing antibody marker as an immune correlate. The design is intended to lay the foundation for a subsequent licensure trial and the development and refinement of future HIV vaccine regimens. Key design features include broad, population-based eligibility criteria; the incorporation of external data; decentralized approaches to recruitment, specimen, and data collection; and strong community partnerships. We compare the approach with alternative trial designs and outline their limitations. The population-based design represents a compelling option for generating credible and generalizable evidence, while enabling future HIV vaccine licensure and development.

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Publication Details

Journal
Vaccines
Published
2026-09-09
DOI
https://doi.org/10.3390/vaccines14090794
Primary Topic
HIV Research and Treatment
Type
article
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A Population-Based HIV Vaccine Efficacy Trial Design: Statistical Framework and Design Considerations

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A Population-Based HIV Vaccine Efficacy Trial Design: Statistical Framework and Design Considerations

Charles Shey Wiysonge, Fei Gao, Derrick Mapp, Kimberly Louis, Holly Janes, Susan Buchbinder, Amelia Mfiki, Blossom Napoleon, Glenda Gray
article en

Abstract

An HIV vaccine will be a critical tool for ending the epidemic, yet the next vaccine efficacy trial is likely five or more years away as the field focuses on the early-phase evaluation and optimization of vaccines that induce broadly neutralizing antibodies. At the same time, the HIV prevention landscape has evolved substantially, with the discovery of highly effective means of preventing HIV, challenging the identification of HIV prevention trial designs that are ethically sound and scientifically robust. We explore a population-based, individually randomized, proof-of-concept trial design for evaluating the efficacy of a future candidate vaccine to prevent HIV acquisition and to validate the neutralizing antibody marker as an immune correlate. The design is intended to lay the foundation for a subsequent licensure trial and the development and refinement of future HIV vaccine regimens. Key design features include broad, population-based eligibility criteria; the incorporation of external data; decentralized approaches to recruitment, specimen, and data collection; and strong community partnerships. We compare the approach with alternative trial designs and outline their limitations. The population-based design represents a compelling option for generating credible and generalizable evidence, while enabling future HIV vaccine licensure and development.

VaccinesVol. 14(9)
South African Medical Research Council (ZA), Cape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa (ZA), Groote Schuur Hospital (ZA), Fred Hutch Cancer Center (US), Shanti Project (US), San Francisco Department of Public Health (US), Aurum Institute (ZA)
Openalex Percentile: Top 12%
HIV Research and Treatment
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