drugset / Trial / NCT02201004
TOFO Insulin Combination Trial
RandomizedParallel-groupDouble-blindTreatment
Summary
Primary Objectives: To assess the effects of tofogliflozin on glycemic control in comparison to placebo as an add-on treatment to insulin treatment in terms of glycated hemoglobin (HbA1c) reduction over a period of 16 weeks in patients with type 2 diabetes mellitus. To assess the safety of tofogliflozin in combination with insulin treatment throughout 52 weeks. Secondary Objectives: To assess the effects of tofogliflozin in comparison to placebo on: * Body weight * Fasting plasma glucose (FPG) * Postprandial plasma glucose (PPG) To assess the long term safety and tolerability of tofogliflozin.
Timeline
- Start
- 2014-06
- Primary completion
- 2016-01
- Completion
- 2016-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | TOFOGLIFLOZIN ANHYDROUS | Other / unclassified | 20 mg | Oral |
| Background | Insulin | Protein / enzyme biologic | — | Subcutaneous |