Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT05719441
PHASE2

A Clinical Trial of Combination HIV-Specific Broadly Neutralizing Monoclonal Antibodies Combined With ART Initiation During Acute HIV Infection to Induce HIV Remission

Sponsor: National Institute of Allergy and Infectious Diseases (NIAID)

View on ClinicalTrials.gov

Summary

A5388 is a phase II, two-arm, randomized, double-blind, placebo-controlled study that will enroll 48 antiretroviral therapy (ART)-naïve adults with acute HIV infection (AHI) in order to determine whether: * Administration of combination HIV-specific broadly neutralizing antibody (bNAb) therapy in addition to ART during acute HIV infection (AHI) will be safe. * Participants who receive combination bNAb therapy in addition to ART during AHI will be more likely to demonstrate a delay in time to HIV-1 RNA ≥1,000 copies/mL for 4 consecutive weeks during an Analytical Treatment Interruption (ATI) compared to participants who receive placebo plus ART. * Participants who receive combination bNAb therapy in addition to ART during AHI will demonstrate lower viral reservoirs and enhanced HIV-specific immunity compared to participants who receive placebo plus ART.

Official title: A Double-Blind, Randomized, Placebo-Controlled Clinical Trial of Combination HIV-Specific Broadly Neutralizing Monoclonal Antibodies Combined With ART Initiation During Acute HIV Infection to Induce HIV Remission

Key Details

Gender

All

Age Range

18 Years - 70 Years

Study Type

INTERVENTIONAL

Enrollment

48

Start Date

2024-08-19

Completion Date

2029-06-18

Last Updated

2026-10-14

Healthy Volunteers

No

Interventions

BIOLOGICAL

VRC07-523LS

10 mg/kg intravenous infusion over approximately 15 to 30 minutes once at entry

BIOLOGICAL

PGT121.414.LS

5 mg/kg intravenous infusion over approximately 30 to 60 minutes once at entry

OTHER

Placebo

Sodium Chloride for Injection USP, 0.9%

DRUG

ART

Bictegravir 50 mg/emtricitabine 200 mg/tenofovir alafenamide 25 mg tablet orally once daily with or without food

Locations (12)

31788, Alabama CRS

Birmingham, Alabama, United States

6101, University of Colorado Hospital CRS

Aurora, Colorado, United States

5802, The Ponce de Leon Center CRS

Atlanta, Georgia, United States

2701, Northwestern University CRS

Chicago, Illinois, United States

31786, New Jersey Medical School Clinical Research Center CRS

Newark, New Jersey, United States

2301, Ohio State University CRS

Columbus, Ohio, United States

6201, Penn Therapeutics CRS

Philadelphia, Pennsylvania, United States

31473, Houston Advancing Research Team CRS

Houston, Texas, United States

1401, University of Washington Positive Research CRS

Seattle, Washington, United States

12201, Instituto de Pesquisas em AIDS do Rio Grande do Sul - IPARGS CRS

Porto Alegre, Brazil

12101, Instituto de Pesquisa Clinica Evandro Chagas (IPEC) CRS

Rio de Janeiro, Brazil

11301, Barranco CRS

Lima, Peru