Safety and Immunotherapeutic Activity of an Anti-PD-1 Antibody (Cemiplimab) in Participants With HIV-1 on Suppressive cART
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
- Study ID
- NCT03787095
- Phase
- PHASE1/PHASE2
- Status
- Terminated
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 64 Years
- Healthy Volunteers
- Not accepted
Interventions
- Cemiplimab — BIOLOGICALAdministered as an intravenous (IV) infusion
- Placebo — BIOLOGICALDiluent for REGN2810, administered as an IV infusion
Study Details
The purpose of this study was to evaluate the safety and immunotherapeutic activity of an anti-PD-1 antibody (cemiplimab) in participants with HIV-1 on suppressive combination antiretroviral therapy (cART).
Key Dates
- Start date
- Aug 13, 2019
- Status verified
- Feb 2022
- Primary completion
- Aug 18, 2020
- Completion
- Aug 18, 2020
Study Design
- Enrollment
- 5 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Cohort 1: CemiplimabParticipants received 0.3 mg/kg of cemiplimab, administered at Day 0 and Week 6 for a total of two infusions. Participants continued their current non-study provided ART regimen.
- Placebo Comparator: Cohort 1: PlaceboParticipants received placebo, administered at Day 0 and Week 6 for a total of two infusions. Participants continued their current non-study provided ART regimen.
Primary Outcome Measure
Count of Participants With a Grade >=3 Adverse Event (AE) or Grade >=1 Immune-related AE (irAE) Related to Study Treatment [ Time Frame: Study Entry through Week 48 or premature discontinuation ]
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Alabama CRS | Birmingham | Alabama | 35294 | - |
| UCSD Antiviral Research Center CRS | San Diego | California | 92103 | - |
| Chapel Hill CRS | Chapel Hill | North Carolina | 27599 | - |
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