Study to Evaluate the Safety and Efficacy of GS-5423 and GS-2872 in Combination With Lenacapavir (GS-6207) in Virologically Suppressed Adults With HIV-1 Infection
Recruiting
18 years - 65 years
All
Phase
1
50 participants needed
1 Location
Brief description of study
The primary objective of this study is to evaluate the safety and tolerability of a combination of the broadly neutralizing antibodies (bNAbs) GS-5423 and GS-2872 in combination with the HIV capsid inhibitor lenacapavir (LEN).
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: HIV-1
-
Age: 18 years - 65 years
-
Gender: All
Male and Female, Age 18-65, On first-line antiretroviral therapy (ART) for ≥ 2 years
Updated on
04 Aug 2024.
Study ID: 849990