drugset / Trial / NCT04811040

Study to Evaluate the Safety and Efficacy of Teropavimab and Zinlirvimab in Combination With Lenacapavir in Virologically Suppressed Adults With HIV-1 Infection

NCT04811040

Phase 1 Completed 32 enrolled Gilead Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the safety and tolerability of a combination of the broadly neutralizing antibodies (bNAbs) teropavimab (formerly GS-5423) and zinlirvimab (formerly GS-2872) in combination with the HIV capsid inhibitor lenacapavir (LEN).

Timeline

Start
2021-04-08
Primary completion
2022-06-09
Completion
2023-10-26

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenacapavir Small molecule 600 mg Oral
Subject Lenacapavir Small molecule 927 mg Oral
Subject Teropavimab Monoclonal antibody 30 mg/kg Intravenous
Subject Zinlirvimab Monoclonal antibody 10 mg/kg Intravenous
Subject Zinlirvimab Monoclonal antibody 30 mg/kg Intravenous