By Maureen M. Goodenow, Ph.D.
May 2020
The study compared the safety and efficacy of long-acting injectable cabotegravir to daily oral pills (Truvada) for pre-exposure prophylaxis (PrEP). PrEP is a strategy in which healthy people use one or more antiretroviral drugs to reduce their risk of getting HIV. During its planned review of the study data, an independent Data and Safety Monitoring Board (DSMB) determined that the long-acting drug was highly effective in the study population, and subsequently recommended that investigators discontinue that arm of the study. Originally, the study was expected to continue until 2021.
A companion study, HPTN 084 , comparing the efficacy and safety of cabotegravir to daily oral Truvada, for HIV prevention among women in sub-Saharan Africa is still underway, and a DSMB review is scheduled for November 2020.
The HPTN 083 outcome enhances the toolkit of prevention options for HIV. Currently, the only FDA-approved PrEP is in the form of a daily oral pill. While pills are effective, daily adherence can pose lifestyle challenges for some people. A long-acting alternative may be more desirable and manageable for some individuals.
We applaud the rigorous work of the HPTN that has led to this great outcome for HIV prevention. The HPTN is a collaborative clinical trials endeavor that is co-funded by several institutes of the National Institutes of Health (NIH): The National Institute of Allergy and Infectious Diseases , National Institute of Mental Health , and National Institute on Drug Abuse . To learn more, visit the HIV Prevention Trials Network . For more information on HPTN 083 and HPTN 084 visit Clinical Trials.gov and use these identifiers NCT02720094 and NCT03164564 , respectively.
Maureen M. Goodenow, Ph.D.
Associate Director for AIDS Research and
Director, Office of AIDS Research
National Institutes of Health