Advancing health research through clinical trials, basic science, community engagement, education, capacity building, and advocacy.

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Our Research Portfolio

Ongoing Studies

Research in progress to advance HIV prevention, long-term health outcomes, and accessible cervical cancer screening.

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Our studies in progress

Generating evidence for healthier communities.

Explore the studies currently being implemented by UVRI-CRP Initiative and its research partners.

01MK8527-010

MK8527-010

Phase 3South AfricaKenyaUganda

A Phase 3, Randomized, Active-Controlled, Double-blind Clinical Study To Evaluate the Efficacy And Safety Of MK-8527 Oral Once-Monthly As HIV-1 Preexposure Prophylaxis in Women

The Study is carried out in countries of South Africa, Kenya and Uganda.

Objectives
  1. To evaluate the efficacy of oral MK-8527 QM compared to FTC/TDF QD for the prevention of HIV-1 infection as assessed by as assessed by the incidence rate per year of adjudicated HIV-1 infections
  2. To evaluate the safety and tolerability of oral MK-8527 QM compared to oral FTC/TDF QD
02PURPOSE 1

PURPOSE 1 Study

Started 202225 centresSouth AfricaUganda

PURPOSE 1 which stands for Phase 3, Double- Blinded, Multicenter, Randomized Study to Evaluate Safety and Efficacy of Twice Yearly Long- Acting Subcutaneous Lenacapavir, and Daily Oral Emtricitabine/ Tenofovir Alafenamide for Pre- Exposure Prophylaxis in Adolescent Girls and Young Women at Risk of HIV Infection started in 2022 and has the main objective of evaluating the efficacy of lenacapavir (LEN) and emitricitabine/ tenofovir alafenamide (F/TAF) in preventing the risk of HIV-1 infection relative to the background HIV-1 incidence rate.

The PURPOSE 1 study includes a cross-sectional study which has the Incidence phase, the Randomized phase a LEN Open Label Extension phase and Pharmacokinetic Tail Phase.

The PURPOSE I study in partnership with Gilead Sciences, Inc. is based in approximately 25 centers in South Africa and Uganda. In Uganda there are three sites that work on the PURPOSE study namely; Makerere- Kalangala, AMBSO and MUJHU with each site recruiting a total number of 250 cisgender Adolescent Girls and Young Women at risk of acquiring HIV-1 infection from the age of 16 to 25 years.

Objectives

The primary objective of the Incidence phase of the study is to estimate the HIV-1 background incidence rate.

  1. To evaluate the efficacy of LEN for HIV-1 pre-exposure prophylaxis (PrEP) in Adolescent girls and Young Women at risk of HIV-1 infection
  2. To evaluate the efficacy of F/TAF for HIV-1 PrEP in AGYW at risk of HIV-1 infection.
03PALLISADE

PALLISADE Study

Started 17 Jan 2025CAB LAHPTN 083HPTN 084

UVRI-CRP Initiative ( formerly UVRI-IAVI HIV Vaccine Program) started implementing ( PALISADE study ) a Long-Term Follow-Up study of Cabotegravir long-acting (CAB LA) for Participants in HPTN 083 and HPTN 084 CAB PrEP Studies at Risk of HIV Acquisition sponsored by ViiV Healthcare UK Limited on 17 Jan 2025

Objectives

The primary objective is to describe new HIV infections in adult and adolescent participants at risk of HIV acquisition included in the HPTN 083 and HPTN 084 studies and their associated sub-studies.

04CHILI

CHILI Project

Started 2021Five-year studyHorizon 2020Four countries

CHILI project which is Community Based HPV screening Implementation in Low- and middle-Income countries, started in 2021. This is a five-year study aimed to evaluate the acceptability, feasibility and cost-effectiveness of the Horizon 2020 ELEVATE cervical cancer screening tool in LMICs.

The concept of the CHILI project is to design a multidisciplinary intervention to enhance screening coverage for cervical cancer, particularly for women in LMICs. The CHILI project supported by the European Union’s Horizon 2020 Framework Program for Research and Innovation Action, is based in Uganda, Mozambique, Ethiopia and Cambodia. For Uganda, the Project is made up of the Formative research component, the Adaptation Protocol that enrolled 112 participants, the Survey and Discrete Choice Experiment that enrolled 600 participants and Piloting of the ELEVATE tool, all from the age of 25 to 65 years and residents of Mukono and Wakiso districts.

It is the intention of the CHILI consortium to develop a strategy that will bring cervical cancer screening to women, and not the other way around. Therefore, the device needs to be adapted and validated in these new contexts. Especially the cost of the device needs to be reduced as to afford scaling-up.

The approach of the CHILI project is three-fold. First, social science investigations will be conducted to understand current screening practices and to define a tailored strategy, including the new screening tool, that can be integrated in the current health system.

Secondly, engineers will validate the HPV self-testing device and will adapt it to reduce the unit price and to enable large-scale manufacturing at an affordable cost. Finally, public health specialists and health economists will evaluate the implementation of the new screening tool during a pilot study to assess its appropriateness and cost-effectiveness.

Objectives
  1. To understand current cervical cancer screening practices and to define new strategies that include the ELEVATE self-sampling test and meet the conditions and requirements of the local context to increase screening coverage in the selected LMICs.
  2. To adapt and upscale the ELEVATE screening device to be used as a universal screening test in LMICs.
  3. To assess the adapted ELEVATE screening device, determining its user acceptability, uptake and cost effectiveness, by implementing and evaluating the new screening strategies in the selected LICs.