Study to Evaluate the Pharmacokinetics, Safety and Tolerability of GSK557296 in Healthy Women Volunteers After Single and Repeat Dosing

PHASE1CompletedINTERVENTIONAL
Enrollment

36

Participants

Timeline

Start Date

August 16, 2012

Primary Completion Date

March 9, 2013

Study Completion Date

March 9, 2013

Conditions
Embryo Transfer
Interventions
DRUG

GSK557296 10 mg

10 mg single oral dose. Each subject will receive 2 tablets of 5 mg GSK557296 four times a day (QID).

DRUG

GSK557296 150 mg

150 mg single oral dose. Each subject will receive multiple tablets of 25 mg GSK557296 either 2, 3 or 4 times a day.

DRUG

GSK557296 dose 3

Dose to be determined as a single dose tablet based on half-life demonstrated in Cohort 1 and Cohort 2.

DRUG

GSK557296 dose 4

Dose to be determined by PK of prior doses, based on half-life demonstrated in prior cohorts.

Trial Locations (1)

21225

GSK Investigational Site, Baltimore

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY

NCT01669083 - Study to Evaluate the Pharmacokinetics, Safety and Tolerability of GSK557296 in Healthy Women Volunteers After Single and Repeat Dosing | Biotech Hunter | Biotech Hunter