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NCT06101329Active, not recruitingPhase 2

Study of Lenacapavir and Emtricitabine/Tenofovir Disoproxil Fumarate (F/TDF) in Prevention of HIV in Cisgender Women in the United States (HPTN 102)

A Phase 2, Open-label, Multicenter, Randomized Study to Evaluate the Pharmacokinetics, Safety, and Acceptability of Twice Yearly Long-acting Subcutaneous Lenacapavir for Pre-Exposure Prophylaxis in Cisgender Women in the United States

Source: ClinicalTrials.gov · Last updated 17 Aug 2026

Brief summary (registry, in English)

The goal of this clinical study is 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 prevention of HIV in the cisgender women in the US. The primary objectives of this study are: 1) to characterize the pharmacokinetics (PK) of LEN in United States (US) cisgender women; 2) to evaluate the safety of LEN and F/TDF for pre-exposure prophylaxis (PrEP) in US cisgender women; and 3) to evaluate the general acceptability of LEN injections and oral F/TDF in US cisgender women.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
253 (actual)
First submitted
20 Oct 2023
Start date
Nov 2023
Primary completion date
Jul 2026
Lead sponsor
Gilead Sciences
Diseases
HIV
NCT number
NCT06101329

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 253
  • From Nov 2023 to the primary completion date, Jul 2026
  • 11 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Self-reported history of previous positive results on an HIV test.
  • Prior use of long-acting systemic pre-exposure prophylaxis (PrEP) (including cabotegravir (CAB) or islatravir studies).

Other illness

  • One or more reactive or positive HIV test result at screening or enrollment, even if HIV infection is not confirmed.
  • 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).
  • Acute viral hepatitis A or acute or chronic hepatitis B or C infection.
  • Severe hepatic impairment or a history of or current clinical decompensated liver cirrhosis (eg, ascites, encephalopathy, variceal bleeding, etc).
    • Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Who the study is looking for

  • Report at least 1 episode of condomless vaginal or anal sex with a cisgender man in the 12 months before enrollment.
  • Hepatitis B virus (HBV) surface antigen (HBsAg) negative.
  • Self-report one or more of the following in the past 12 months (except for incarceration, which could have occurred in the past 5 years):
    • 1\) Noninjection recreational drug use (ecstasy, cocaine, crack cocaine, methamphetamine, ketamine, 3,4-methylenedioxy-methamphetamine, or prescription drugs apart from those prescribed by a licensed provider); 2) Alcohol dependence (defined as Cut Down, Annoyed, Guilty, and Eye Opener score of 2); binge-drinking, defined as 4 or more drinks at a time; 3) History of STIs, such as gonorrhea, chlamydia, or syphilis; 4) Exchange of sex for commodities, such as drugs, money, or shelter; 5) Incarceration (jail or prison \> 24 hours within the past 5 years); 6) Two or more sexual partners who were assigned male at birth; 7) Sexual partner assigned male at birth with history of either injection or noninjection recreational drug use, sexually transmitted infections (STIs), human immunodeficiency virus (HIV) diagnosis or unknown HIV status, additional sex partners during the course of his sexual relationship with the individual, or incarceration (jail or prison \> 24 hours within the past 5 years)
  • 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).

Age in the registry: 18 years to - · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (11)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Ponce de Leon Center Clinical Research Site
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
UAB, 1917 Research Clinic
Coordinator of this site? Confirm its status
BirminghamUnited StatesUnknown status
Fenway Health
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status
NC TraCS Institute - CTRC University of North Carolina at Chapel Hill
Coordinator of this site? Confirm its status
Chapel HillUnited StatesUnknown status
Rutgers New Jesey Medical School - Clinical Research Center
Coordinator of this site? Confirm its status
NewarkUnited StatesUnknown status
Cornell Clinical Trials Unit, New York Presbyterian Hospital - Weill Cornell Medicine
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Harlem Prevention Center CRS
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Penn Prevention Research Unit
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
UCSD AntiViral Research Center (AVRC)
Coordinator of this site? Confirm its status
San DiegoUnited StatesUnknown status
ICAP at Columbia University- Bronx Prevention Center
Coordinator of this site? Confirm its status
The BronxUnited StatesUnknown status
George Washington University- Medical Faculty Associates
Coordinator of this site? Confirm its status
Washington D.C.United StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.