Safety, Tolerability and Acceptability of Long-Acting Cabotegravir (CAB LA) for the Prevention of HIV Among Adolescent Females

PHASE2CompletedINTERVENTIONAL
Enrollment

55

Participants

Timeline

Start Date

November 4, 2020

Primary Completion Date

January 10, 2023

Study Completion Date

January 10, 2023

Conditions
HIV Infections
Interventions
DRUG

Oral cabotegravir (CAB)

30 mg tablets

DRUG

CAB LA

Administered as one 3 mL (600 mg) IM injection in the gluteal muscle at two time points 4 weeks apart and every 8 weeks thereafter

DRUG

Oral tenofovir disoproxil fumarate/emtricitabine (TDF/FTC)

300 mg/200 mg fixed-dose combination tablets

Trial Locations (3)

2001

Ward 21 CRS, Johannesburg

23491

MU-JHU Research Collaboration (MUJHU CARE LTD) CRS, Kampala

Unknown

Spilhaus CRS, Harare

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

ViiV Healthcare

INDUSTRY

collaborator

Bill and Melinda Gates Foundation

OTHER

lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH