drugset / Trial / NCT00781391

Global Study to Assess the Safety and Effectiveness of Edoxaban (DU-176b) vs Standard Practice of Dosing With Warfarin in Patients With Atrial Fibrillation

NCT00781391 ↗

Phase 3 Completed 21105 enrolled Daiichi Sankyo The TIMI Study Group · collab
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This study is to demonstrate the safety and efficacy profile, in two different dose regimens of Edoxaban (DU-176b), (an investigational new drug being tested for the prevention of stroke/systemic embolic events (SEE)), in individuals with atrial fibrillation. Patients will be randomized to one of three treatment groups: High Dose Regimen, Low Dose Regimen, \& Warfarin. The expected duration of the study is 24 months.

Timeline

Start
2008-11
Primary completion
2013-04
Completion
2013-05

Outcome

Sources disagree · no verdict is set; each source's reading is shown below

registry High Dose Edoxaban/Placebo Warfarin vs Warfarin/Placebo Edoxaban; p <.0001; Hazard Ratio (HR) 0.79 (97.5% CI .632 to .985) reads as mixed primary results NCT00781391 ↗

registry If upper limit of CI of HR was below 1.38, then non-inferiority to warfarin was established for group. reads as mixed primary results NCT00781391 ↗

registry High Dose Edoxaban/Placebo Warfarin vs Warfarin/Placebo Edoxaban; p = .081; Hazard Ratio (HR) 0.87 (99% CI .709 to 1.068); Log Rank reads as mixed primary results NCT00781391 ↗

release “edoxaban met the primary efficacy endpoint of non-inferiority compared to warfarin for the prevention of stroke or systemic embolic events (SEE)” reads as met primary endpoint daiichisankyo.com ↗

release “In ENGAGE AF-TIMI 48, SAVAYSA was non-inferior to warfarin in the overall study population for the primary efficacy endpoint of stroke or SE.” reads as met primary endpoint daiichisankyo.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Edoxaban Small molecule 30 mg Oral
Subject Edoxaban Small molecule 60 mg Oral
Comparator Warfarin Small molecule — Oral