RecruitingPhase 1NCT07349758
Evaluation of Single Dosing With Two F/TAF Tablets Among Healthy Volunteers
DD-PrEP: Pharmacokinetic Evaluation of Single Dosing With Two F/TAF Tablets Among Healthy Volunteers
Sponsor
Johns Hopkins University
Enrollment
24 participants
Start Date
Jan 6, 2026
Study Type
INTERVENTIONAL
Conditions
Summary
The goal of this study is to evaluate the pharmacokinetics of a one-time dosing of two F/TAF tablets over a 14-day period.
Eligibility
Min Age: 18 Years
Plain Language Summary
Simplified for easier understanding
This study is testing whether taking two tablets of F/TAF (a combination HIV prevention medication also called Descovy) in a single dose provides effective drug levels for preventing HIV. This explores a simplified dosing approach that could be relevant for on-demand HIV pre-exposure prophylaxis (PrEP).
**You may be eligible if...**
- You are 18 or older and currently HIV-negative
- You are in generally good health
- Your kidneys are functioning well (eGFR of 70 or higher)
- You agree to use condoms during the study and to not take other PrEP medications outside the study
**You may NOT be eligible if...**
- You have used F/TDF or F/TAF (oral PrEP) in the past 2 months
- You test positive for HIV or hepatitis B
- You have had gastrointestinal surgery that could affect how the drug is absorbed
- You are pregnant or breastfeeding
- You are taking medications known to affect drug absorption
Talk to your doctor to see if this trial is right for you.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
DRUGtenofovir alafenamide [TAF] 50 mg/emtricitabine [FTC] 400mg
One-time dose of two F/TAF tablets
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07349758
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