drugset / Trial / NCT04150068

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

NCT04150068

Phase 2/3 Active not recruiting 72 enrolled Gilead Sciences
RandomizedSequentialQuadruple-blindTreatment

Summary

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).

Timeline

Start
2019-11-21
Primary completion
2020-10-05
Completion
2027-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenacapavir Small molecule 927 mg Oral