drugset / Trial / NCT01525238

PK Study of Dapagliflozin in Pediatric Subjects With T2DM

NCT01525238

Phase 1 Completed 53 enrolled AstraZeneca Bristol-Myers Squibb · collab
RandomizedParallel-groupOpen-labelOther

Summary

The primary purpose of this study is to evaluate the pharmacokinetics (PK) of Dapagliflozin in pediatric subjects with type 2 diabetes mellitus (T2DM)

Timeline

Start
2012-07-01
Primary completion
2014-09-01
Completion
2014-09-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Dapagliflozin Small molecule 2.5 mg Oral
Subject Dapagliflozin Small molecule 5 mg Oral
Subject Dapagliflozin Small molecule 10 mg Oral