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.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
56
Oral Solution, Oral, 0.3 mg, once daily, 1 day
Oral Solution, Oral, 1.0 mg, once daily, 1 day
Oral Solution, Oral, 3 mg, once daily, 1 day
Profil Institute For Clinical Research, Inc. (Picr)
Chula Vista, California, United States
Clinical Pharmacology Of Miami Inc.
Miami, Florida, United States
Elite Research Institute
Miami, Florida, United States
Safety and Tolerability of the investigational drug, as assessed by adverse event monitoring, physical examinations, clinical laboratory determinations, electrocardiograms (ECG), and vital sign assessments
Time frame: Within 5 days of study drug administration
Exposure to the investigational drug and its metabolites
Time frame: Within 2 days after study drug administration
Pharmacodynamic activity of the investigational drug on biomarkers
Time frame: Within 2 days after study drug administration
Excretion of the investigational drug and metabolites from the body
Time frame: Within 2 days after study drug administration
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Oral Solution, Oral, 10 mg, once daily, 1 day
Oral Solution, Oral, 30 mg, once daily, 1 day
Oral Solution, Oral , 75 mg, once daily, 1 day
Oral Solution, Oral, 150 mg, once daily, 1 day
Oral Solution, Oral, 300 mg, once daily, 1 day
Capsule, Oral, (TBD), once daily, 2 days
Oral Solution, Oral, 0mg, once daily, 1 day
Capsule, Oral, (TBD), once daily, 2 days