To Evaluate Safety, Tolerability, Plasma Drug Levels And Other Biological Effects In Healthy Volunteers

PHASE1TerminatedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

February 28, 2010

Primary Completion Date

June 30, 2010

Study Completion Date

June 30, 2010

Conditions
Healthy
Interventions
DRUG

PF-03382792 Cohort 1

First cohort for: Single oral ascending dose of PF-03382792, formulated in solution.

DRUG

PF-03382792 Cohort 2

Second cohort for: Single oral ascending dose of PF-03382792, formulated in solution.

DRUG

PF-03382792

Optional cohort 3: Single oral ascending dose of PF-03382792, formulated in solution.

DRUG

Food Effect cohort

Single oral dose, cross-over to determine effect of food on PF-03382792 pharmacokinetics. Dose will be decided after reviewing data from the ascending dose portion.

DRUG

CSF cohort

Single oral dose of PF-03382792 formulated in solution. Dose will be decided after reviewing data from the ascending dose portion.

Trial Locations (1)

06511

Pfizer Investigational Site, New Haven

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY