drugset / Trial / NCT03417076

Absolute Bioavailability Study With Bexagliflozin

NCT03417076 ↗

Phase 1 Withdrawn Theracos
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the absolute bioavailability of bexagliflozin following a single oral dose co-administered with an intravenous dose.

Timeline

Start
2018-08-01
Primary completion
2018-09-16
Completion
2018-09-16

Outcome

Outcome not reported

Stopped (Business): “Sponsor decision to not initiate study due to sufficient bioavailability information”

Drugs

EvaluationDrugModalityDoseRoute
Subject Bexagliflozin Small molecule 30 ug Oral
Subject Bexagliflozin Small molecule 20 mg Oral