Plain-English translation of NCT07672717 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Phase 1 — Testing in a small group (usually 20–80 people) to find a safe dose and watch for side effects.
This trial is testing cabotegravir (Apretude), an FDA-approved injectable medication given every two months to prevent HIV infection. Researchers want to understand how well this medication reaches the tissues in the rectum and genital areas where HIV transmission actually occurs, and whether using hormone therapies affects how the medication works in your body.
While this medication has proven effective at preventing HIV in large studies, researchers still have important unanswered questions about how it penetrates the specific tissues where HIV enters the body and how it might interact with hormone therapies that some people use. This study will directly measure the medication's levels in blood, tissue samples, and genital secretions to fill these knowledge gaps.
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You would start with screening visits to confirm you are HIV-negative and collect baseline information about your hormones. At a baseline visit, you would have blood drawn and provide tissue biopsies from your rectum and cervix (if female) so researchers can test how your body responds to HIV before receiving the medication. One week later, you would receive the first injection of the medication, with follow-up injections every two months. Throughout the study, you would have additional visits involving blood draws, more tissue samples, and monitoring for any side effects.
AI-generated summary from trial data · Aug 7, 2026 · Not medical advice
United States
Phase
Safety & dosing
Sponsor
Johns Hopkins University
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID)
Enrollment target
~32 participants
Started
July 2026
Primary completion
December 2030
Age range
19 Years and older
Last updated on clinicaltrials.gov in July 2026.
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Central contact
Pooja Akoijam
Johns Hopkins School of Medicine
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