Clinical trial

A Phase 3, Double-Blind, Multicenter, Randomized Study to Evaluate the Efficacy and Safety of Subcutaneous Twice Yearly Long-Acting Lenacapavir for HIV Pre-Exposure Prophylaxis in Cisgender Men, Transgender Women, Transgender Men, and Gender Nonbinary People ≥ 16 Years of Age Who Have Sex With Male Partners and Are at Risk for HIV Infection

Name
GS-US-528-9023
Description
The goal of this clinical study is to test how well the study drug, lenacapavir (LEN), works in preventing the risk of HIV.
Trial arms
Trial start
2021-06-28
Estimated PCD
2025-01-01
Trial end
2027-04-01
Status
Active (not recruiting)
Phase
Early phase I
Treatment
Oral Lenacapavir (LEN)
Tablets administered orally without regard to food
Arms:
Blinded Phase: LEN + Placebo-to-match (PTM) F/TDF, LEN Open-Label Extension (OLE) Phase
Other names:
GS-6207
F/TDF
Tablets administered orally
Arms:
Blinded Phase: Placebo LEN + F/TDF, PK Tail Phase
Other names:
Truvada®
Sub-cutaneous (SC) Lenacapavir (LEN)
Administered via SC injections
Arms:
Blinded Phase: LEN + Placebo-to-match (PTM) F/TDF, LEN Open-Label Extension (OLE) Phase
Other names:
GS-6207
Placebo SC LEN
Administered via SC injections
Arms:
Blinded Phase: Placebo LEN + F/TDF
PTM F/TDF
Tablets administered orally
Arms:
Blinded Phase: LEN + Placebo-to-match (PTM) F/TDF
PTM Oral LEN
Tablets administered orally
Arms:
Blinded Phase: Placebo LEN + F/TDF
F/TAF (for US participants only)
F/TAF tablets administered orally once daily
Arms:
PK Tail Phase
Size
3295
Primary endpoint
Incidence Phase: Background HIV Incidence per 100-Person-Years (PY)
At Screening
Randomized Phase: Number of Participants with Diagnosis of HIV-1 Infection
When all participants have completed a minimum of 52 weeks of follow-up in the study, or permanent discontinuation, whichever occurs first (maximum approximately 130 weeks)
Eligibility criteria
Key Inclusion Criteria: Incidence Phase * CGM, TGW, TGM, and GNB who have condomless receptive anal sex with partners assigned male at birth and are at risk for HIV infection. * HIV-1 status unknown at screening and no prior HIV-1 testing within the last 3 months. * Sexually active with ≥ 1 partner assigned male at birth (condomless receptive anal sex) in the last 12 months and 1 of the following: * Condomless receptive anal sex with ≥ 2 partners in the last 12 weeks. * History of syphilis, rectal gonorrhea, or rectal chlamydia in the last 24 weeks. * Self-reported use of stimulants with sex in the last 12 weeks. Randomized Phase * Negative local rapid fourth generation HIV-1/2 Ab/Ag, central fourth generation HIV-1/2 Ab/Ag, and HIV-1 RNA quantitative nucleic acid amplification testing (NAAT). * Estimated glomerular filtration rate (eGFR) ≥ 60 mL/min at screening according to the Cockcroft-Gault formula for creatinine clearance (CLcr). Key Exclusion Criteria: Incidence Phase * Prior use of HIV PrEP (including F/TDF or F/TAF) or HIV postexposure prophylaxis (PEP) in the past 12 weeks or any prior use of long-acting systemic PrEP (including cabotegravir or islatravir). * Prior recipient of an HIV vaccine or HIV broadly neutralizing antibody formulation. Randomized Phase * Acute viral hepatitis A, B or C or evidence of chronic hepatitis B or C infection. * Severe hepatic impairment or a history of or current clinical decompensated liver cirrhosis. Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE3'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'DOUBLE', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR']}}, 'enrollmentInfo': {'count': 3295, 'type': 'ACTUAL'}}
Updated at
2023-12-28

1 organization

8 products

1 indication

Organization
Gilead Sciences
Product
F/TDF
Product
Placebo
Product
PTM F/TDF
Product
F/TAF
Product
PTM