drugset / Trial / NCT01152385
Japan Dose Regimen Study of AZD1656 in Japanese Type 2 Diabetes Mellitus Patients
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | AZD1656 | Small molecule | 80 mg | Oral |
| Subject | AZD1656 | Small molecule | 140 mg | Oral |
| Subject | AZD1656 | Small molecule | 200 mg | Oral |