Safety and Immune Response of BMS-936559 in HIV-Infected People Taking Combination Antiretroviral Therapy

PHASE1CompletedINTERVENTIONAL
Enrollment

8

Participants

Timeline

Start Date

June 30, 2014

Primary Completion Date

November 30, 2015

Study Completion Date

November 30, 2015

Conditions
HIV Infections
Interventions
DRUG

BMS-936559

0.3 mg/kg, 1 mg/kg, 3 mg/kg, or 10 mg/kg of BMS-936559, depending on which cohort participants are enrolled in, administered as an intravenous (IV) infusion

DRUG

Placebo for BMS-936559

Sodium chloride for injection 0.9%, USP, administered as an IV infusion

Trial Locations (5)

27599

Chapel Hill CRS, Chapel Hill

37204

Vanderbilt Therapeutics (VT) CRS, Nashville

45219

Cincinnati Clinical Research Site, Cincinnati

80045

University of Colorado Hospital CRS, Aurora

63110-1010

Washington University Therapeutics (WT) CRS, St Louis

All Listed Sponsors
lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH

NCT02028403 - Safety and Immune Response of BMS-936559 in HIV-Infected People Taking Combination Antiretroviral Therapy | Biotech Hunter | Biotech Hunter