Study of Lenacapavir and Emtricitabine/Tenofovir Disoproxil Fumarate (F/TDF) for Prevention of HIV in People Who Inject Drugs (HPTN 103)
Condition(s) studied
Investigational drug(s) / intervention(s)
Lenacapavir Injection: Administered subcutaneously
Lenacapavir Tablet: Administered orally
Emtricitabine/tenofovir disoproxil fumarate (F/TDF): Administered orally
Study 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.
Eligibility
Primary outcome measure(s)
- Pharmacokinetic (PK) Parameter: Ctrough for Lenacapavir (LEN): LEN Plasma concentration at the End of the Dosing Interval (Week 26) — Week 26
- PK Parameter: Ctrough for LEN: LEN Plasma concentration at the End of the Dosing Interval (Week 52) — Week 52
- Percentage of Participants Experiencing Treatment-emergent Adverse Events (TEAEs) — First dose date up to 30 days post last dose at Week 52
- Percentage of Participants Experiencing Treatment-emergent Clinical Laboratory Abnormalities with LEN and F/TDF — First dose date up to 30 days post last dose at Week 52
Trial sites (9)
| Facility | City | Region | Status |
|---|---|---|---|
| UCLA Vine Street Clinic | Los Angeles | California | |
| UCSD AntiViral Research Center (AVRC) | San Diego | California | |
| University of Miami - Converge Miami Building | Miami | Florida | |
| Johns Hopkins Medicine Institute for Clinical and Translational Research, Clinical Research | Baltimore | Maryland | |
| Rutgers New Jersey Medical School, Department of Medicine | Newark | New Jersey | |
| ICAP at Columbia University- Bronx Prevention Center | The Bronx | New York | |
| University of Pennsylvania, Division of Infectious Diseases Penn Prevention Research Unit | Philadelphia | Pennsylvania | |
| Houston AIDS Research Team CRS | Houston | Texas | |
| West Virginia University | Morgantown | West Virginia |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06101342 on ClinicalTrials.gov ↗ ← All trials in the USA