Evaluating the Safety and Pharmacokinetics of Maraviroc in HIV-1-Exposed Infants at Risk of Acquiring HIV-1 Infection

PHASE1CompletedINTERVENTIONAL
Enrollment

47

Participants

Timeline

Start Date

June 5, 2017

Primary Completion Date

September 6, 2019

Study Completion Date

November 20, 2019

Conditions
HIV Infections
Interventions
DRUG

Maraviroc

8 mg/kg oral solution as a single dose.

DRUG

Maraviroc

8 mg/kg oral solution given twice daily.

Trial Locations (9)

1862

Soweto IMPAACT CRS, Johannesburg

4001

Umlazi CRS, Durban

10700

Siriraj Hospital ,Mahidol University NICHD CRS, Bangkok

20200

Kenya Medical Research Institute / Walter Reed Project Clinical Research Center, Kericho CRS, Kericho

60612

Rush Univ. Cook County Hosp. Chicago NICHD CRS, Chicago

80045

Univ. of Colorado Denver NICHD CRS, Aurora

90089

Usc La Nichd Crs, Los Angeles

60614-3393

Lurie Children's Hospital of Chicago (LCH) CRS, Chicago

38105-3678

St. Jude Children's Research Hospital CRS, Memphis

Sponsors
All Listed Sponsors
collaborator

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

NIH

collaborator

ViiV Healthcare

INDUSTRY

collaborator

GlaxoSmithKline

INDUSTRY

lead

National Institute of Allergy and Infectious Diseases (NIAID)

NIH