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Study identifier: NCT04150068 Synced from ClinicalTrials.gov · August 05, 2026
● Active Not Recruiting

Study to Evaluate the Safety and Efficacy of Lenacapavir (GS-6207) in Combination With an Optimized Background Regimen (OBR) in Heavily Treatment Experienced Participants Living With HIV-1 Infection With Multidrug Resistance

Condition: HIV-1-infection  ·  Sponsor: Gilead Sciences

PhasePhase 2/Phase 3
Planned participants72
Who can joinAll sexes, 12 Years to no upper limit
Healthy volunteersNo

About this study

The primary objective of this study is to evaluate the antiviral activity of lenacapavir (formerly GS-6207) administered as an add-on to a failing regimen for 14 days (functional monotherapy) in people with human immunodeficiency virus type 1 (HIV-1) (PWH) with multi-drug resistance (MDR).

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

Always discuss trial participation with your own doctor first.

Locations (75)

Ruane Clinical Research Group IncLos Angeles, California, United States
Mills Clinical ResearchLos Angeles, California, United States
Eisenhower Health Center at RimrockPalm Springs, California, United States
One Community HealthSacramento, California, United States
Yale University; School of MedicineNew Haven, Connecticut, United States
Washington Health InstituteWashington D.C., District of Columbia, United States
Midland Florida Clinical Research Center, LLCDeLand, Florida, United States
Gary J. Richmond, M.D., P.A.Fort Lauderdale, Florida, United States
Midway Immunology and Research CenterFt. Pierce, Florida, United States
Floridian Clinical ResearchHialeah, Florida, United States
AIDS Healthcare Foundation - South BeachMiami Beach, Florida, United States
Orlando Immunology CenterOrlando, Florida, United States

+ 63 more locations — full list on the registry record.

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