Study to Evaluate the Safety and How the Body Handles a Single Dose of Subcutaneous (SC) and Intravenous (IV) Budigalimab in Adult Participants Living With Human Immunodeficiency Virus (HIV)

PHASE1CompletedINTERVENTIONAL
Enrollment

33

Participants

Timeline

Start Date

March 15, 2021

Primary Completion Date

October 11, 2022

Study Completion Date

October 11, 2022

Conditions
Human Immunodeficiency Virus (HIV)
Interventions
DRUG

Budigalimab

Subcutaneous (SC)

DRUG

Placebo

Subcutaneous (SC)

DRUG

Budigalimab

Intravenous (IV)

DRUG

Placebo

Intravenous (IV)

Trial Locations (10)

75246

North TX Infectious Diseases /ID# 224494, Dallas

90036

Ruane Clinical Research Group /ID# 224496, Los Angeles

93301

Franco Felizarta, Md /Id# 223931, Bakersfield

94115-3037

Quest Clinical Research /ID# 223925, San Francisco

78705-3326

Central Texas Clinical Research /ID# 223937, Austin

77401-4528

St. Hope Foundation, Inc. /ID# 224492, Bellaire

77098-3900

The Crofoot Research Center, Inc /ID# 224493, Houston

98104-3595

Peter Shalit, M.D. /ID# 224801, Seattle

00716-0377

Ponce Medical School Foundation /ID# 224230, Ponce

00935

Puerto Rico AIDS Clinical Trials Unit CRS /ID# 223936, San Juan

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AbbVie

INDUSTRY