A Trial To Assess The Safety, Tolerability, Pharmacokinetics, And Pharmacodynamics Of Single Doses Of PF-04937319 In Subjects With Type 2 Diabetes Mellitus

PHASE1CompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

February 28, 2010

Primary Completion Date

May 31, 2010

Study Completion Date

May 31, 2010

Conditions
Type 2 Diabetes Mellitus
Interventions
DRUG

Placebo

Placebo to match PF-04937319 will be provided.

DRUG

PF-04937319

The initial planned dosing schedule is: 10, 30, 100, 200, and 400 mg, with one cohort to be determined. Doses shown may be adjusted upwards or downwards and may be adjusted to include intermediate doses. All doses will be administered as a single oral dose as a powder-in-capsule (PIC) formulation. PF-04937319 will be supplied as 10 mg and 80 mg (and potentially 1 mg) PIC.

Trial Locations (3)

33169

Elite Research Institute, Miami

85013

Dedicated Phase 1, Phoenix

90630

West Coast Clinical Trials, LLC, Cypress

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY