drugset / Trial / NCT06250504

Long-Acting HIV Pre-Exposure Prophylaxis Integrated With Sexual and Reproductive Health - cRCT

NCT06250504

Phase 3 Recruiting 2052 enrolled Africa Health Research Institute
RandomizedParallel-groupDouble-blindPrevention

Summary

The goal of this hybrid (1a) Cluster Randomised Controlled Trial phase 3B trial is to evaluate the effectiveness and implementation of offering a choice of HIV Pre-Exposure Products (PrEP) through community-based sexual and reproductive health services, on PrEP uptake and retention, and population prevalence of sexually transmissible HIV amongst adolescents and young adults living in rural South Africa. Researchers will compare adding the choice of long-acting PrEP, i.e. two monthly injectable cabotegravir (CAB LA) or dapiravine vaginal ring and HIV post exposure prophylaxis packs to daily oral PrEP integrated with community-based SRH in the 20 intervention clusters with standard of care (SoC), daily oral PrEP integrated with community-based SRH in the 20 control clusters, on uptake and retention on PrEP. We hypothesise that offering a choice of long-acting or oral PrEP and PEP within the community-based delivery of SRH services will overcome the challenges and barriers to effective use of oral daily PrEP and lead to a population-level effect on uptake and retention on PrEP and thus the prevalence of sexually transmissible HIV amongst 15-30 year olds living in rural KwaZulu-Natal, South Africa.

Timeline

Start
2024-02-27
Primary completion
2026-04-30
Completion
2026-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Cabotegravir Small molecule 600 mg
Subject Dolutegravir Other / unclassified
Subject Lamuvidine Unknown
Subject Tenofovir disoproxil fumarate Small molecule Oral
Subject dapivirine Small molecule 25 mg Other
Subject emtricitabine Other / unclassified Oral