Long-acting HIV Treatments: Study Design, Logistics, and Access

Author:

Murdock Nicholas A1,Alajaji Nayri E1,Schaefer Robin1ORCID,Boone Cheriko A2,Campo Rafael E3,Dore Gregory J4,Gandhi Monica5ORCID,Gorospe J Rafael6,Gulick Roy M7,Hodder Sally L8,Liu Jonathan9,Rhee Martin S10,Rooney James F10,Vannappagari Vani11,Wilkin Timothy7,Miller Veronica1

Affiliation:

1. Forum for Collaborative Research, University of California , Berkeley, Washington, DC , USA

2. TAG Treatment Action Group Inc. , New York, New York , USA

3. Merck & Co., Inc. , Upper Gwynedd, Pennsylvania , USA

4. The Kirby Institute, University of New South Wales , Sydney, NSW , Australia

5. Department of Medicine, University of California at San Francisco (UCSF) , San Francisco, California , USA

6. Office of AIDS Research, National Institutes of Health , Bethesda, Maryland , USA

7. Department of Medicine, Weill Cornell Medicine , New York, New York , USA

8. West Virginia Clinical and Translational Science Institute, West Virginia University School of Medicine , Morgantown, West Virginia , USA

9. University of Southern California , Los Angeles, California , USA

10. Gilead Sciences , Foster City, California , USA

11. ViiV Healthcare , Durham, North Carolina , USA

Abstract

Abstract New long-acting HIV treatment products have the potential to change the HIV epidemic in the United States and globally. Phase 3 clinical trials of HIV treatments tend to underrepresent populations bearing a disproportionate burden of the HIV epidemic—including women, racial minorities, trans and gender-diverse people, older adults, the unhoused, people who inject drugs, those in rural areas, individuals with mental illness, and other marginalized groups. These populations commonly face significant challenges in adhering to daily HIV treatment regimens. Conducting clinical trials of long-acting treatment targeting specific unmet medical needs of these populations can improve understanding of optimal care approaches, broaden the indication for use of long-acting products, and inform treatment guidelines, all of which can influence reimbursement and access policies. Innovative trial designs and programmatic implementation can improve inclusivity for long-acting therapy. This article summarizes discussions of a multistakeholder workshop on study designs for long-acting HIV treatments.

Funder

HIV Forum of the Forum for Collaborative Research

Gilead Sciences

Merck Sharp & Dohme LLC

Merck & Co

ViiV Healthcare

Publisher

Oxford University Press (OUP)

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