GSK1349572 Relative Bioavailability Study

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

April 30, 2010

Primary Completion Date

June 30, 2010

Study Completion Date

July 31, 2010

Conditions
Infection, Human Immunodeficiency Virus
Interventions
DRUG

GSK1349572 formulation AP

GSK1349572 50 mg single dose fasted.

DRUG

GSK1349572 formulation AW

GSK1349572 formulation AW 50 mg single dose in Part A and 75 to 200 mg fasted or with moderate or high fat meal in Part B.

DRUG

GSK1349572 formulation AX

GSK1349572 formulation AX 50 mg in Part A and 75-200 mg fasted or with a moderate or high fat meal in Part B

Trial Locations (1)

78744

GSK Investigational Site, Austin

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

ViiV Healthcare

INDUSTRY

NCT01098513 - GSK1349572 Relative Bioavailability Study | Biotech Hunter | Biotech Hunter