Safety and Tolerability of Ascending Intravenous Doses of PF-05231023 In Adult Subjects With Type 2 Diabetes

PHASE1CompletedINTERVENTIONAL
Enrollment

50

Participants

Timeline

Start Date

July 31, 2011

Primary Completion Date

May 31, 2012

Study Completion Date

May 31, 2012

Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG

PF-05231023

5 mg IV twice a week for 4 weeks

DRUG

PF-05231023

25 mg IV twice a week for 4 weeks

DRUG

PF-05231023

100 mg IV twice a week for 4 weeks

DRUG

PF-05231023

200 mg IV twice a week for 4 weeks

OTHER

Placebo

0.9% w/v sodium chloride injection, United States Pharmacopeia (USP), twice a week IV for 4 weeks

Trial Locations (5)

33143

Pfizer Investigational Site, South Miami

33169

Pfizer Investigational Site, Miami

66212

Pfizer Investigational Site, Overland Park

78229

Pfizer Investigational Site, San Antonio

91911

Pfizer Investigational Site, Chula Vista

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT01396187 - Safety and Tolerability of Ascending Intravenous Doses of PF-05231023 In Adult Subjects With Type 2 Diabetes | Biotech Hunter | Biotech Hunter