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Study of Lenacapavir and Emtricitabine/Tenofovir Disoproxil Fumarate (F/TDF) for Prevention of HIV in People Who Inject Drugs (HPTN 103)
Sponsor: Gilead Sciences
Summary
The goals of this clinical study are to look at how lenacapavir (LEN) passes through the body and to assess the safety of LEN and emtricitabine/tenofovir disoproxil fumarate (F/TDF) for pre-exposure prophylaxis (PrEP) in people who inject drugs (PWID) in the United States (US). The primary objectives of this study are to characterize the pharmacokinetics (PK) of LEN and to evaluate the safety of LEN and F/TDF for PrEP in US PWID.
Official title: A Phase 2, Open-Label, Multicenter, Randomized Study to Evaluate the Pharmacokinetics and Safety of Twice Yearly Long-Acting Subcutaneous Lenacapavir for Pre-Exposure Prophylaxis in People Who Inject Drugs
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
181
Start Date
2023-12-13
Completion Date
2028-01
Last Updated
2026-03-02
Healthy Volunteers
Yes
Interventions
Lenacapavir Injection
Administered subcutaneously
Lenacapavir Tablet
Administered orally
Emtricitabine/tenofovir disoproxil fumarate (F/TDF)
Administered orally
Locations (9)
UCLA Vine Street Clinic
Los Angeles, California, United States
UCSD AntiViral Research Center (AVRC)
San Diego, California, United States
University of Miami - Converge Miami Building
Miami, Florida, United States
Johns Hopkins Medicine Institute for Clinical and Translational Research, Clinical Research
Baltimore, Maryland, United States
Rutgers New Jersey Medical School, Department of Medicine
Newark, New Jersey, United States
ICAP at Columbia University- Bronx Prevention Center
The Bronx, New York, United States
University of Pennsylvania, Division of Infectious Diseases Penn Prevention Research Unit
Philadelphia, Pennsylvania, United States
Houston AIDS Research Team CRS
Houston, Texas, United States
West Virginia University
Morgantown, West Virginia, United States