drugset / Trial / NCT01152385

Japan Dose Regimen Study of AZD1656 in Japanese Type 2 Diabetes Mellitus Patients

NCT01152385 ↗

Phase 2 Completed 224 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to compare the effect on glucose control of 3 different AZD1656 dosing regimens with placebo in Japanese type 2 diabetes mellitus (T2DM) patients, as evaluated by the change in HbA1c from baseline to the end of treatment at 4 months.

Timeline

Start
2010-05
Primary completion
2011-05
Completion
2011-05

Outcome

Missed primary endpoint

paper The changes from baseline to 4 months in HbA1c were not significant for the AZD1656 40-200 mg group versus placebo [mean (95% CI) placebo-corrected change: -0.22 (-0.65, 0.20)%; p = 0.30]. PMID 23522182 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD1656 Small molecule 80 mg Oral
Subject AZD1656 Small molecule 140 mg Oral
Subject AZD1656 Small molecule 200 mg Oral