drugset / Trial / NCT02390050

A Dose Range Finding Study to Evaluate the Effect of Bexagliflozin Tablets in Subjects With Type 2 Diabetes Mellitus

NCT02390050

Phase 2 Completed 292 enrolled Theracos
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study was to investigate the effect of bexagliflozin in lowering hemoglobin A1c (HbA1c) levels in patients with type 2 diabetes mellitus (T2DM). Bexagliflozin is an orally administered drug for the treatment of T2DM and is classified as a Sodium Glucose co-Transporter 2 (SGLT2) Inhibitor. This study was to enroll both treatment naive and those subjects previously treated with one oral hypoglycemic agent (OHA). Approximately 320 subjects eligible for randomization was to receive bexagliflozin tablets, 5, 10, 20 mg or placebo, once daily for 12 weeks in an outpatient setting.

Timeline

Start
2015-05-12
Primary completion
2016-06-03
Completion
2016-06-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bexagliflozin Small molecule 5 mg Oral
Comparator Bexagliflozin Small molecule 10 mg Oral
Comparator Bexagliflozin Small molecule 20 mg Oral