Safety Study of BMS-903452 in Healthy Subjects (Panel 1-7) & Relative Bioavailability of the Crystalline and Amorphous Forms of BMS-903452 [Panels 4, 6, 11 & 12(Part A)], and Subjects With Type 2 Diabetes Mellitus (Part B)

PHASE1CompletedINTERVENTIONAL
Enrollment

104

Participants

Timeline

Start Date

November 30, 2010

Primary Completion Date

January 31, 2012

Study Completion Date

January 31, 2012

Conditions
Diabetes
Interventions
DRUG

BMS-903452

Solution, Oral, 0.1 mg, once daily, 1 day

DRUG

BMS-903452

Solution, Oral, 0.6 mg, once daily, 1 day

DRUG

BMS-903452

Suspension, Oral, 3.0 mg, once daily, 1 day

DRUG

BMS-903452

Suspension, Oral, 10 mg, once daily, 1 day

DRUG

BMS-903452

Suspension, Oral, 30 mg, once daily, 1 day

DRUG

BMS-903452

Suspension, Oral, 60 mg, once daily, 1 day

DRUG

BMS-903452

Suspension, Oral, 120 mg, once daily, 1 day

DRUG

Placebo

Solution, Oral, 0 mg, once daily, 1 day

DRUG

Placebo

Suspension, Oral, 0 mg, once daily, 1 day

DRUG

BMS-903452

Suspension using crystalline form, Oral, 10 mg, once daily, 1 day

DRUG

BMS-903452

Suspension using crystalline form, Oral, 60 mg, once daily, 1 day

DRUG

Placebo

Suspension using crystalline form, Oral, 0 mg, once daily, 1 day

DRUG

BMS-903452

Solution, Oral, 0.6 mg, once daily, 1 day

DRUG

BMS-903452

Suspension, Oral, 10 mg, once daily, 1 day

DRUG

BMS-903452

Suspension, Oral, 120 mg, once daily, 1 day

Trial Locations (2)

33025

Comprehensive Phase One, Miramar

78744

Ppd Development, Lp, Austin

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY