CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 219 enrolled
Drug / intervention
BMS-986036 +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02097277
NCT02097277Phase 2Completed

A Randomized, Double-blind, Placebo-controlled, Parallel-group, Multiple Dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamic Effects of BMS-986036 in Obese Adults With Type-2 Diabetes

Bristol-Myers Squibb·interventional·Posted Mar 27, 2014·Updated Jul 31, 2019

In Brief

A Phase 2 clinical trial evaluating BMS-986036 and Placebo (Matching with BMS-986036) for Diabetes Mellitus Type 2. Completed, enrolled 219 participants across 16 sites in 2 countries.

Detailed Summary

The purpose of this study is to assess the potential of BMS-986036 for treatment obese adults with type-2 diabetes.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, United States
Collaborators--

Timeline

Phase 2CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedMar 27, 2014
Enrollment StartApr 15, 2014
Primary CompletionSep 22, 2015
Study CompletionMay 17, 2016
TodayJul 2, 2026
Enrollment to primary: 1.4 yearsPosted 12.3 years ago

Interventions

BMS-986036biological

Placebo (Matching with BMS-986036)biological