Single Ascending Dose Study of BMS-820132 in Patients With Type 2 Diabetes

NCT01105429 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2011-03-09

No results posted yet for this study

Summary

BMS-820132 is an investigational new drug being developed by BMS for treating Type 2 diabetes. The purpose of this study is to test the safety/tolerability (potential side effects) of single doses of the investigational new drug, as well as the amount of study drug in the blood, in subjects with type 2 diabetes.

Conditions

  • Diabetes Mellitus, Non-Insulin-Dependent

Interventions

DRUG

BMS-820132

Oral Solution, Oral, 0.3 mg, once daily, 1 day

DRUG

BMS-820132

Oral Solution, Oral, 1.0 mg, once daily, 1 day

DRUG

BMS-820132

Oral Solution, Oral, 3 mg, once daily, 1 day

DRUG

BMS-820132

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

DRUG

BMS-820132

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

DRUG

BMS-820132

Oral Solution, Oral , 75 mg, once daily, 1 day

DRUG

BMS-820132

Oral Solution, Oral, 150 mg, once daily, 1 day

DRUG

BMS-820132

Oral Solution, Oral, 300 mg, once daily, 1 day

DRUG

BMS-820132

Capsule, Oral, (TBD), once daily, 2 days

DRUG

Placebo

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

DRUG

Placebo

Capsule, Oral, (TBD), once daily, 2 days

Sponsors & Collaborators

Principal Investigators

  • Bristol-Myers Squibb · Bristol-Myers Squibb

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-05-31
Primary Completion
2010-10-31
Completion
2010-10-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01105429 on ClinicalTrials.gov