HIV Pre-Exposure Prophylaxis

10

Review clinical trials related to HIV Pre-Exposure Prophylaxis. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Clinical Trial of MK-8527 and Rifampin in Adult Participants With Latent Tuberculosis Infection (MK-8527-019)

Researchers are studying MK-8527, a new medicine for preventing HIV-1 (human immunodeficiency virus type 1) infection and want to learn if MK-8527 can be given together with rifampin. Rifampin is commonly used to treat people with latent tuberculosis infection (LTBI). The main goal of this study is to learn what happens to MK-8527 in the body over time when given with and without the medication rifampin in participants with LTBI.

Participants needed: 14
Trial details
Phase: Phase 1Age: 18-60Biological sex: AllType: InterventionalSponsor: Merck Sharp & Dohme LLCUpdated: Jul 2, 2026
Eligibility criteria

Has a diagnosis of untreated latent tuberculosis infection (LTBI) [+3]

Has a diagnosis of LTBI made in the context of an outbreak/contact-tracing inves... [+5]

Status: Recruiting

A Study of MK-8527 to Prevent Human Immunodeficiency Virus Type 1 (HIV-1) (MK-8527-010)

Researchers are looking for new medicines to prevent HIV-1 (Human Immunodeficiency Virus Type 1) infection. The goals of this study are to learn: * If taking MK-8527 once a month works to prevent HIV-1 infection better than a standard (usual) pre-exposure prophylaxis (PrEP) taken once a day * About the safety of MK-8527 and if people tolerate it

Participants needed: 4,580
Trial details
Phase: Phase 3Age: 16-30Biological sex: FemaleType: InterventionalSponsor: Merck Sharp & Dohme LLCUpdated: Jun 29, 2026Locations: 30
Eligibility criteria

Is confirmed Human Immunodeficiency Virus (HIV)-uninfected based on negative HIV... [+3]

Has hypersensitivity or other contraindication to any component of the study int... [+5]

Status: Recruiting

A Clinical Study of MK-8527 to Prevent Human Immunodeficiency Virus Type 1 (HIV-1) (MK-8527-011)

Researchers are looking for new medicines to prevent HIV-1 (Human Immunodeficiency Virus Type 1) infection. The goals of this study are to learn: * If taking MK-8527 once a month works to prevent HIV-1 infection as well as or better than a standard (usual) pre-exposure prophylaxis (PrEP) taken once a day * About the safety of MK-8527 and if people tolerate it

Participants needed: 4,390
Trial details
Phase: Phase 3Age: 16+Biological sex: AllType: InterventionalSponsor: Merck Sharp & Dohme LLCUpdated: Jun 29, 2026Locations: 81
Eligibility criteria

Is confirmed HIV-uninfected based on negative HIV-1/HIV-2 test results [+3]

Has hypersensitivity or other contraindication to any component of the study int... [+6]

Status: Recruiting

HIV Pre-Exposure Prophylaxis (PrEP) Linkage With Immediate Medications in the Emergency Department Study

Our primary objective is to increase HIV pre-exposure prophylaxis (PrEP) awareness and uptake among people who want, need, or would benefit from PrEP in Dallas, TX through a pilot program of immediate PrEP prescribing in the Parkland Memorial Hospital Emergency Department (ED) with linkage to PrEP clinic. Leveraging the previous work of the Parkland Center for Clinical Innovation (PCCI) which created an automated electronic health record (EHR) based HIV prediction tool and prior success with a robust ED HIV navigation program, a PrEP navigator would approach patients in the Parkland ED for PrEP initiation. Through standard care prescribing by their ED clinician, subjects would leave the ED with a prescription for rapid-start oral PrEP and a clinic appointment to persist on the PrEP modality of their choice which will include long-acting injectable options.

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Texas Southwestern Medical CenterUpdated: Jun 2, 2026Locations: 1
Eligibility criteria

Able to comprehend and provide signed, written informed consent prior to initiat... [+6]

Known diagnosis of HIV [+5]

Status: Recruiting

Enhancing PrEP Uptake and Retention Among Latine TGW and GBM in the South Using Long-Acting Injectable PrEP

The purpose of this project is to test a culturally-tailored, community-delivered long-acting injectable PrEP (lenacapavir) program for Latine gay and bisexual men (GBM) and transgender women (TGW). The objective is to evaluate whether this intervention demonstrates greater persistence on lenacapavir for Latine GBM and TGW compared with what has been observed historically at the Duke PrEP Clinic.

Participants needed: 100
Trial details
Phase: Phase 4Age: 18+Biological sex: MaleType: InterventionalSponsor: Duke UniversityUpdated: Feb 2, 2026Locations: 1
Eligibility criteria

Participants must be assigned male sex at birth. [+6]

Individuals living with HIV. [+4]

Status: Not yet recruiting

Long-Acting Injectable HIV PrEP PROs

The goal of this observational study is to learn about the real world effectiveness, patient satisfaction and clinical outcomes of LAI PrEP with lenacapavir (LEN) versus cabotegravir (CAB) through surveys and interviews. Participants receiving or initiating LAI PrEP part of their regular medical care will complete surveys and interviews at three study visits over the course of 12 months.

Participants needed: 128
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Anupama Raghuram MDUpdated: Jan 30, 2026Locations: 3
Eligibility criteria

Adults aged 18 and older [+5]

HIV diagnosis prior to enrollment [+4]

Status: Not yet recruiting

Trauma-informed, Resilience-based Telehealth Intervention for Improving HIV Prevention and HCV Care for Persons Who Inject Drugs in the Deep South (Pilot Testing: Aim3)

Evaluate the feasibility, acceptability, and usability of the intervention (primary outcomes) and coping skills and resilience (secondary outcomes) of the telehealth intervention over two months (8 weekly sessions) in a waitlist-controlled, randomized pilot trial using a cross-over design among 40 PWID. The primary outcomes will be feasibility, acceptability, and usability of the intervention. Secondary outcomes will be increased coping skills and resilience, which in turn, will increase status neutral HIV and HCV care and MOUD uptake (longer-term outcomes). Outcomes will be assessed using pre- and post-intervention surveys.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of GeorgiaUpdated: Dec 18, 2025Locations: 1
Eligibility criteria

People who actively inject drugs verified by visible injection stigmata (needle... [+3]

Living with HIV [+2]

Status: Not yet recruiting

Optimizing PrEP Uptake for African American Women in the South by Empowering Women to Make Informed HIV Prevention and Sexual Health Choices

Pilot testing of EMPOWER, a group sexual health intervention, to increase uptake and persistence of PrEP

Participants needed: 80
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: University of GeorgiaUpdated: Sep 15, 2025Locations: 1
Eligibility criteria

Identification as cis-gendered Black woman; [+5]

Cognitive or mental health condition that limits the ability to provide informed... [+3]

Status: Recruiting

Vienna HIV Infection Via Sex Study

The main objective of this prospective observational cohort study is to investigate the epidemiology, the risk factors and ultimately the incidence of novel HIV infections among individuals at high risk for acquiring HIV via sex practices.

Participants needed: 500
Trial details
Age: 18-100Biological sex: AllType: ObservationalSponsor: Medical University of ViennaUpdated: Apr 13, 2022Locations: 1Duration: 5 Years
Eligibility criteria

High risk for acquiring HIV defined as followed: HIV-negative MSM and transgende... [+2]