A Multiple Dose Study To Determine Safety, Tolerability, and Pharmacokinetics Of PF-04634817 In Healthy Adult Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

June 30, 2010

Primary Completion Date

October 31, 2010

Study Completion Date

October 31, 2010

Conditions
Healthy
Interventions
DRUG

PF-04634817

Oral solution of PF-04634817 at 3 mg will be given once daily for 14 days.

DRUG

PF-04634817

Oral solution of PF-04634817 at 3 mg will be given once daily for 14 days.

DRUG

PF-04634817

Oral solution of PF-04634817 at 30 mg will be given once daily for 14 days.

DRUG

PF-04634817

Oral solution of PF-04634817 at 100 mg will be given once daily for 14 days.

DRUG

PF-04634817

Oral solution of PF-04634817 at 300 mg will be given once daily for 14 days.

DRUG

PF-04634817

Cohort will only be dosed if necessary. Dose selected for this cohort may be a repeat of a previous cohort or intermediate dose not to exceed 300 mg.

Trial Locations (1)

06511

Pfizer Investigational Site, New Haven

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY