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)

Johns Hopkins University School of Medicine

Baltimore, Maryland, United States

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NCT07349758


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