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HIV Prevention Clinical Trials

Reviewed by TrialFinderData Editorial Team · Updated

6 recruiting trials for HIV Prevention. Eligibility criteria explained in plain English.

TrialFinderData lists 6 HIV Prevention clinical trials drawn from ClinicalTrials.gov, all of which are currently recruiting participants.

Every phased trial in this set is Phase 4 (1 of the listed studies); the remaining records are observational or have no phase recorded on ClinicalTrials.gov.

Research is led by Institute of HIV Research and Innovation Foundation, Thailand (1), University of California, Los Angeles (1), University of Colorado, Denver (1), among the most active sponsors registered for these trials.

The most frequently studied intervention is Understanding of chemsex patterns, impacts, and service needs among transgender persons (behavioral, 1 trial), followed by Mobile Enhanced Prevention Support (MEPS), Control.

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.
6
Total Trials
6
Recruiting Now
0
Phase 3 Trials
6
Sponsors

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Recruiting Trials

Clinical trial data sourced from the ClinicalTrials.gov registry, maintained by the National Library of Medicine. Always consult your doctor before considering any clinical trial.

RECRUITINGNCT07505875

Pre-implementation Study to Develop Trans-tailored Services for Transgender Persons in Relation to chemsEX

The study is a pre-implementation cross-sectional study exploring chemsex behaviors among transgender persons and gathering perspectives from multiple stakeholders to inform the...

Sponsor: Institute of HIV Research and Innovation Foundation, ThailandEnrolling: 501 location
RECRUITINGNCT07433985

California MEPS Hub

The California Hub for HIV/SUD Prevention Research with Reentry Populations addresses the question: "Can the evidence-based MEPS intervention be adapted and implemented at a range...

Sponsor: University of California, Los AngelesEnrolling: 3183 locations
RECRUITINGNCT06656676

WePrEP: Developing a PrEP Shared Decision-making Tool for Transgender Women

HIV prevalence among transgender women (TW) in the United States is high (\~14%). The best way to reduce HIV incidence in this population is to link TW to HIV pre-exposure...

Sponsor: University of Colorado, DenverEnrolling: 751 location
RECRUITINGNCT07136363

RESTORE Study R61 Phase: Recovery and Engagement for Stimulant Users on Re-entry

Justice-involved individuals face disproportionately high rates of stimulant use disorder and HIV, along with disrupted access to HIV treatment and prevention services like ART...

Sponsor: University of Texas Southwestern Medical CenterEnrolling: 402 locations
RECRUITINGPhase 4NCT06485154

Post-Injectable Cabotegravir Antiretroviral Salvage Strategy Options Trial

This is a single-arm, open-label, effectiveness study designed to evaluate the use of Tenofovir, Lamivudine, and Dolutegravir in people with newly diagnosed HIV-1 infection...

Sponsor: University of Witwatersrand, South AfricaEnrolling: 1003 locations
RECRUITINGNCT07194902

HIV Self-testing for Partners of HIV-uninfected Postpartum Women

The purpose of this study is to test the feasibility and acceptability of a combination intervention to promote HIV self-testing (HIVST) for Partners and PrEP uptake for...

Sponsor: Massachusetts General HospitalEnrolling: 1201 location

Frequently Asked Questions

There are currently 6 clinical trials for HIV Prevention, with 6 actively recruiting participants. These include trials across all phases from early-stage Phase 1 to late-stage Phase 3.

To join a clinical trial for HIV Prevention, review the eligibility criteria on the trial detail pages, then talk to your doctor about whether a trial is right for you. Your doctor can help you evaluate the potential benefits and risks.

Phase 3 trials are large-scale studies that test whether a treatment is effective and monitor side effects. There are 0 Phase 3 trials for HIV Prevention, representing treatments closest to potential FDA approval.

Clinical trials follow strict safety protocols overseen by Institutional Review Boards (IRBs) and the FDA. Participants are monitored closely and can withdraw at any time. Always discuss risks and benefits with your healthcare provider before enrolling.

Sources: ClinicalTrials.gov, FDA
Last updated:

Trial data sourced from the ClinicalTrials.gov API. This site does not provide medical advice, always talk to your doctor about clinical trial participation.