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 — BIOLOGICAL
    Administered as an intravenous (IV) infusion
  • Placebo — BIOLOGICAL
    Diluent 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: Cemiplimab
    Participants 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: Placebo
    Participants 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)

FacilityCityStateZIPSite coordinators
Alabama CRSBirminghamAlabama35294-
UCSD Antiviral Research Center CRSSan DiegoCalifornia92103-
Chapel Hill CRSChapel HillNorth Carolina27599-

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