A Healthy Volunteer Trial to Gain Information About the Blood Concentrations of PF-06412562 After Oral Administration of a Modified Release Formulation in Fasted and Fed Conditions

PHASE1CompletedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

September 30, 2014

Primary Completion Date

October 31, 2014

Study Completion Date

October 31, 2014

Conditions
Healthy
Interventions
DRUG

3 mg PF-06412562 MR tablets_Fasted

A single modified release tablet with 3 mg PF-06412562 administered after an overnight fast

DRUG

2 x 15 mg PF-06412562 MR tablets_Fasted

Two 15 mg PF-06412562 modified release tablets administered after an overnight fast

DRUG

2 x 15 mg PF-06412562 MR tablets_Fed

Two 15 mg PF-06412562 modified release tablets administered after a high fat breakfast

DRUG

10 mg PF-06412562 IR tablets

a single immediate release tablet of 10 mg PF-06412562 after an overnight fast

Trial Locations (1)

B-1070

Pfizer Clinical Research Unit, Brussels

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY