Ireland
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Active, not recruiting Phase 2

Study of Lenacapavir and Emtricitabine/Tenofovir Disoproxil Fumarate (F/TDF) for Prevention of HIV in People Who Inject Drugs (HPTN 103)

NCT06101342 · tracked via the Priya Life Science USA tracker
Phase
Phase 2
Started
2023-12-13
Last updated
2026-08-13

Condition(s) studied

Pre-Exposure Prophylaxis of HIV Infection

Investigational drug(s) / intervention(s)

Lenacapavir Injection →Lenacapavir Tablet →Emtricitabine/tenofovir disoproxil fumarate (F/TDF) →

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

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Key Inclusion Criteria: * Urine drug screen positive for any drug of misuse including, but not limited to, opioids (eg, fentanyl, heroin), stimulants (eg, cocaine, amphetamines), psychoactive drugs (eg, benzodiazepines), or a combination of these drugs. * Evidence of recent injection (eg, track marks). * Self-report of injection paraphernalia sharing in the prior 30 days. * Hepatitis B virus (HBV) surface antigen (HBsAg) negative. * Negative local rapid HIV-1/2 antibody (Ab)/antigen (Ag) test, central HIV-1/2 Ab/Ag, and HIV-1 RNA quantitative nucleic acid amplification testing (NAAT). * Estimated glomerular filtration rate (GFR) at least 60 mL/min at screening according to the Cockcroft-Gault formula for creatinine clearance (CLcr). Key Exclusion Criteria: * Self-reported history of previous positive results on an HIV test. * Any reactive or positive HIV test result at screening or enrollment, even if HIV infection is not confirmed. * Coenrollment in any other interventional research study or other concurrent studies that may interfere with this study (as provided by self-report or other available documentation) without prior approval from the Medical Monitor/Joint Clinical Management Committee while participating in this study. * Past or current participation in HIV vaccine or HIV broadly neutralizing antibody study unless individual provides documentation of receipt of placebo (ie, not active product). * Prior use of long-acting systemic pre-exposure prophylaxis (PrEP) (including cabotegravir (CAB) or islatravir studies). * Acute viral hepatitis A or acute or chronic hepatitis B or C infection. * Have a suspected or known active, serious infection(s) (eg, active tuberculosis, etc). * Evidence of moderate or severe liver fibrosis or a history of or current clinical decompensated liver cirrhosis (eg, ascites, encephalopathy, variceal bleeding). In individuals with active hepatitis C, Fibrosis-4 (FIB-4) score \> 3.25 (formula provided below). Note: Other protocol defined Inclusion/Exclusion criteria may apply.

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)

FacilityCityRegionStatus
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
Official registry record

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