A Study to Evaluate the Pharmacokinetics of an Oral Contraceptive When Co-administered With GSK2248761 in Healthy Adult Female Subjects.

PHASE1TerminatedINTERVENTIONAL
Enrollment

13

Participants

Timeline

Start Date

September 14, 2010

Primary Completion Date

February 9, 2011

Study Completion Date

February 9, 2011

Conditions
Infection, Human Immunodeficiency VirusHIV Infections
Interventions
DRUG

YASMIN

YASMIN for 21 days

DRUG

GSK2248761

200 mg GSK2248761 taken on Days 1 - 10 or Days 12 - 21

OTHER

Placebo

Placebo taken on Days 1 - 10 or Days 12 - 21

Trial Locations (1)

58104

GSK Investigational Site, Fargo

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

ViiV Healthcare

INDUSTRY