Implementing Oral (Event-driven and Daily) and Long-acting Pre-Exposure Prophylaxis in Mobile Men in Sub-Saharan Africa

ConditionHIV
Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexMale
Age18-60
SponsorMRC/UVRI and LSHTM Uganda Research Unit

About this trial

Title: Implementing oral (event-driven and daily) and long-acting Pre-exposure prophylaxis (PrEP) in mobile men in Sub-Saharan Africa

Design: A mixed method, multi-setting, multi-country, phase 3b, open-label, hybrid type 2 implementation and effectiveness randomized controlled trial (RCT). The trial will be carried out in 400 HIV negative men aged 18+ years in South Africa and Uganda. Men will be randomized 1:1 to either Group A: oral Tenofovir disoproxil fumarate/emtricitabine (TDF-FTC) PrEP (event-driven or daily) or Group B: Long-acting injectable cabotegravir (CAB-LA) over 9-months. After 9-months participants from both groups will be offered choice of PrEP (oral TDF-FTC or CAB-LA) for a further 9-months, with the ability to change choice as required. Various strategies to support PrEP adoption, initiation, and persistence will be implemented, monitored, and reported on using a RE-AIM (Reach, Effectiveness, Adoption, Implementation, and Maintenance) implementation science framework.

Treatment: CAB-LA or oral TDF-FTC Duration: 18 months

Eligibility criteria

Qualifiers

Able and willing to provide informed consent

Aged 18 years and above on the day of screening

Willing to have a HIV test and receive the test results

Male at birth

Disqualifiers

Known HIV infection

Confirmed HIV-positive test result, indeterminate HIV test result, and/or signs and symptoms of an acute HIV infection

Body weight less than 35Kg at baseline

Allergy to any of the study products

Trial design

Treatments tested in this trial

  • Tenofovir disoproxil fumarate/emtricitabine (TDF-FTC), cabotegravir (CAB-LA)
  • Cabotegravir (CAB-LA), Tenofovir disoproxil fumarate/emtricitabine (TDF-FTC)

Treatment groups

400 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

MRC/UVRI and LSHTM Uganda Research Unit

Lead sponsor

King's College London

Collaborator

London School of Hygiene and Tropical Medicine

Collaborator

Africa Health Research Institute

Collaborator

Wits Health Consortium (Pty) Ltd

Collaborator

University College, London

Collaborator

Ministry of Health, Uganda

Collaborator

Desmond Tutu HIV Foundation

Collaborator

Assistance Publique - Hôpitaux de Paris

Collaborator