drugset / Trial / NCT02201004

TOFO Insulin Combination Trial

NCT02201004

Phase 4 Completed 211 enrolled Sanofi Kowa Company, Ltd. · collab
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

EvaluationDrugModalityDoseRoute
Subject TOFOGLIFLOZIN ANHYDROUS Other / unclassified 20 mg Oral
Background Insulin Protein / enzyme biologic Subcutaneous