drugset / Trial / NCT02268214

Dapagliflozin Evaluation in Patients With Inadequately Controlled Type 1 Diabetes

NCT02268214 ↗

Phase 3 Completed 833 enrolled AstraZeneca Bristol-Myers Squibb · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine if adding dapagliflozin to insulin is a safe and effective therapy to improve glycemic control in patients with type 1 diabetes.

Timeline

Start
2014-11-11
Primary completion
2017-01-04
Completion
2017-08-25

Outcome

Met primary endpoint

registry analysis (superiority test); Dapagliflozin 5 mg + Insulin vs Placebo + Insulin; p <0.0001; Mean Difference (Final Values) -0.42 (95% CI -0.56 to -0.28); RMM NCT02268214 ↗

registry analysis (superiority test); Dapagliflozin 10 mg + Insulin vs Placebo + Insulin; p <0.0001; Median Difference (Final Values) -0.45 (95% CI -0.58 to -0.31); RMM NCT02268214 ↗

paper At week 24, both doses of dapagliflozin significantly reduced HbA1c compared with placebo PMID 28919061 ↗

Publications

Drugs

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