drugset / Trial / NCT02460978

Dapagliflozin Evaluation in Patients With Inadequately Controlled Type 1 Diabetes

NCT02460978 ↗

Phase 3 Completed 815 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
2015-07-08
Primary completion
2017-09-02
Completion
2018-04-18

Outcome

Met primary endpoint

paper At week 24, dapagliflozin significantly decreased HbA1c (primary outcome; difference vs. placebo: dapagliflozin 5 mg -0.37% [95% CI -0.49, -0.26], PMID 30026335 ↗

registry analysis (superiority test); DAPA 5 MG + INS vs PLA + INS; p <0.0001; Mean Difference (Final Values) -0.37 (95% CI -0.49 to -0.26); Mixed Models Analysis NCT02460978 ↗

Publications

Drugs

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