An injection that lasts eight weeks has proven 90% more effective in HIV prevention in women than a pill that needs to be taken daily

Researchers from the HIV Prevention Trials Network (HPTN) announced on Tuesday that data from the clinical trial of the pre-exposure prophylaxis (PrEP) regimen of long-acting cabotegravir injections once every eight weeks showed it was safe and superior to the daily oral tenofovir/emtricitabine (TDF/FTC), currently used for HIV prevention among women in sub-Saharan Africa.

The trial – known as the HPTN 084 trial and described as a game changer – was headed by Dr Sinead Delany-Moretlwe, a research professor at the University of the Witwatersrand and director of research at the Wits Reproductive Health and HIV Institute (Wits RHI).

This finding was made on 5 November during a planned interim review of the HPTN 084 study data by an independent Data and Safety Monitoring Board (DSMB).

Consequently, the DSMB recommended that the study sponsor – the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health – stop the blinded phase of the trial, which was originally designed to continue through 2022, and share the results. NIAID has accepted the DSMB’s recommendations and is releasing the results now to serve the interests of public health. The study investigators will report more detailed information about the study findings, including more comprehensive data, as soon as is feasible.

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“The results from HPTN 084 are incredibly important for women in Africa where lowering HIV incidence remains a priority,” said HPTN 084 protocol chair Delany-Moretlwe.

Taking a daily pill is challenging

“We know that adherence to a daily pill continues to be challenging, and an effective injectable product such as long-acting CAB is a very important additional HIV-prevention option for them. We are grateful to the women who volunteered for this study and the research staff, as this study would not have been possible without their commitment to HIV prevention.”

Overall, HPTN 084 enrolled 3 223 cisgender women at research sites in Botswana, Eswatini, Kenya, Malawi, South Africa, Uganda and Zimbabwe. Fifty-seven percent of the participants were under the age of 25, the average age of participants was 26 years, 82% were not living with a partner, 55% reported two or more partners in the past month, and 34% reported having a primary partner who is living with HIV or having an unknown HIV status.

A total of 38 HIV infections occurred during follow-up, with four infections in the CAB LA arm (incidence rate 0,21%) and 34 infections in the TDF/FTC arm (incidence rate 1,79%). The hazard ratio in the CAB LA versus TDF/FTC arm was 0,11 (95% CI 0.04-0.32).

Approximately nine times more incident HIV infections occurred in the TDF/FTC arm than in the CAB arm. These results meet the statistical criteria for superiority of CAB LA compared to TDF/FTC in the HPTN 084 study population. The higher-than-expected level of adherence to TDF/FTC throughout the study and overall low incidence rate in both arms of the study clearly demonstrate both drugs were highly effective at preventing HIV acquisition.

Wits University has long been recognised as a global leader in HIV research and has contributed a vast amount of knowledge in the fight against the pandemic.

World-class research from Africa

“This announcement demonstrates the important role that research entities and research-intensive universities play in transforming society and saving human lives. Universities like Wits continue to generate high-quality, locally-relevant knowledge that match and exceed global standards. Congratulations to the Wits RHI team for leading world-class research from Africa that addresses the burden of disease on the continent – this incredible breakthrough will certainly save the lives of many women living in sub-Saharan Africa, and beyond,” said Professor Zeblon Vilakazi, vice-chancellor and principal designate of Wits University.

“In the past 30 years, Wits researchers and clinicians have been at the forefront of the global fight against HIV. The outcome of this research is again a confirmation that South Africa has the ability to compete and collaborate with the best in the world. It is research such as this that will contribute to saving and improving the lives of millions of people around the world – and especially in Africa. This outcome makes all the time, hard work and money invested in research efforts truly worthwhile,” said Professor Martin Veller, dean of the Faculty of Health Sciences at Wits University.

“The remarkably low risk of becoming infected by HIV while on long-acting cabotegravir amongst study participants makes this modality of prophylaxis clinically, very attractive.”

The HPTN 084 results, along with the recent positive opinion of the dapivirine (DPV) ring by the European Medicines Agency (EMA), represent a real opportunity to change the course of the HIV epidemic for women in sub-Saharan Africa.

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Milestone for prevention

“These results are a milestone for prevention of HIV among women at risk of HIV worldwide and especially for women in sub-Saharan Africa. If we are to turn the tide on the HIV epidemic, we will need prevention options that work for women in sub-Saharan Africa. These findings provide great hope and motivation for additional studies to show safety and acceptability in adolescents, pregnant and breastfeeding women,” said Professor Helen Rees, executive director of Wits RHI.

Earlier this year, a sibling study called the HPTN 083 clinical trial showed that a PrEP regimen containing CAB LA injected once every eight weeks was superior to daily oral TDF/FTC for HIV prevention among cisgender men and transgender women who have sex with men.

“The results from HPTN 084 along with the HPTN 083 results released earlier this year show how far we have come in the fight against HIV. A highly effective product like CAB LA that does not require a daily pill can be an important part of ending the epidemic globally,” said Dr Myron Cohen, HPTN co-principal investigator and director of the Institute for Global Health at the University of North Carolina in Chapel Hill.

Availability and cost

When the treatment will be made available and what it will cost will only be determined later, as the research is still ongoing, Delany-Moretlwe said in response to a question. “The company that manufactures cabotegravir has not allocated a cost yet, but what they have articulated is their commitment to access, particularly to low-income countries in the region where HIV is most prevalent.”

The HPTN 084 study is jointly funded through a unique partnership of NIAID, NIMH the Bill & Melinda Gates Foundation, and ViiV Healthcare. Study drugs are provided by ViiV Healthcare and Gilead Sciences, Inc.

Read the HIV Prevention Trials Network fact sheet here.

About HPTN

The HIV Prevention Trials Network (HPTN) is a worldwide collaborative clinical trials network that brings together investigators, ethicists, community members and other partners to develop and test the safety and efficacy of interventions designed to prevent the acquisition and transmission of HIV. NIAID, NIMH, Office of The Director, and NIDA, all part of NIH, co-fund the HPTN. The HPTN has collaborated with more than 85 clinical research sites in 19 countries to evaluate new HIV prevention interventions and strategies in populations that bear a disproportionate burden of infection.

The HPTN research agenda – more than 50 trials ongoing or completed with over 161 000 participants enrolled and evaluated – is focused primarily on the use of integrated strategies: use of antiretroviral drugs (antiretroviral therapy and pre-exposure prophylaxis); interventions for substance abuse, particularly injection drug use; behavioural risk reduction interventions and structural interventions.

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Author: News24.com