drugset / Trial / NCT03739996
Long-Acting Cabotegravir Plus VRC-HIVMAB075-00-AB (VRC07-523LS) for Viral Suppression in Adults Living With HIV-1
Phase 2
Completed
75 enrolled
National Institute of Allergy and Infectious Diseases (NIAID)
ViiV Healthcare · collab
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study was to assess the safety, tolerability, antiviral activity, and pharmacokinetics of long-acting cabotegravir (CAB LA) plus the broadly neutralizing monoclonal antibody VRC-HIVMAB075-00-AB (VRC07-523LS), in adults living with HIV-1 with suppressed plasma viremia.
Timeline
- Start
- 2019-12-31
- Primary completion
- 2024-04-29
- Completion
- 2024-04-29
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cabotegravir | Small molecule | 30 mg | Oral |
| Subject | Cabotegravir | Small molecule | 400 mg | Oral |
| Subject | VRC07-523LS | Monoclonal antibody | 40 mg/kg | Intravenous |