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Safety Study of MucoCept-CVN

NCT07181486

This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .

Summary

MucoCept-CVN uses a Lactobacillus strain native to the human vagina that is modified into a live biotherapeutic product (LBP) that continuously expresses a potent anti-HIV drug. If research shows that MucoCept-CVN is safe and effective, it could become a self-renewing, female-initiated prevention product for women that promotes vaginal health and provides protection from HIV.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • HIV -1 Infection

Eligibility basics and study details

Study type
Interventional
Phase
Phase 1
Ages
18 to 45 years
Sex
Female
Healthy volunteers
Accepted
Sponsor
Craig Cohen, MD, MPH
Last updated on ClinicalTrials.gov
September 11, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

California · 1

  • UCSF Zuckerberg San Francisco General Hospital · San Francisco, CA

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.