drugset / Trial / NCT03557658

Safety and Efficacy of Bexagliflozin in Subjects With Moderate Hepatic Impairment

NCT03557658

Phase 1 Completed 16 enrolled Theracos
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to examine the drug exposure and drug effects on subjects with moderate hepatic impairment after a single oral dose of bexagliflozin tablets, 20mg. The study will also evaluate how safe the study drug is and how well the study drug is tolerated in subjects with moderate hepatic impairment.

Timeline

Start
2018-07-26
Primary completion
2018-12-26
Completion
2018-12-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Bexagliflozin Small molecule 20 mg Oral