Status:

COMPLETED

Efficacy and Safety Study of Canagliflozin (TA-7284) in Combination With Insulin in Patients With Type 2 Diabetes Mellitus

Lead Sponsor:

Tanabe Pharma Corporation

Conditions:

Type 2 Diabetes Mellitus

Eligibility:

All Genders

20+ years

Phase:

PHASE4

Brief Summary

The purpose of this study is to evaluate the efficacy and safety of Canagliflozin (TA-7284) in combination with Insulin in patients with type 2 Diabetes for 16 weeks administration.

Detailed Description

This is a randomized, 2-arm, parallel group, double blind study to evaluate the efficacy and safety of Canagliflozin (TA-7284) in Japanese patients with type 2 diabetes mellitus, who are receiving tre...

Eligibility Criteria

Inclusion

  • Patients who has been receiving a stable dose and regimen of insulin over 12 weeks before administration of investigational dug
  • Patients who are under dietary management and taking therapeutic exercise for diabetes over 12 weeks before administration of investigational drug
  • Patients with HbA1c of ≥7.5% and \<10.5%
  • Patients who were not administered diabetes therapeutic drugs prohibited for concomitant use within 12 weeks before administration of investigational drug

Exclusion

  • Patients with type 1 diabetes mellitus, diabetes mellitus resulting from pancreatic disorder, or secondary diabetes mellitus (Cushing's syndrome, acromegaly, etc.)
  • Patients with severe diabetic complications (proliferative diabetic retinopathy, stage 4 nephropathy, or serious diabetic neuropathy)
  • Patients with hereditary glucose-galactose malabsorption or primary renal glucosuria
  • Patients with systolic blood pressure of ≥160 mmHg or diastolic blood pressure of ≥100 mmHg
  • Patients with serious renal or hepatic disease
  • Patients with eGFR of \<45 mL/min/1.73 m2
  • Patients who are the excessive alcohol addicts
  • Patients who are pregnant, lactating and probably pregnant patients and patients who can not agree to contraception

Key Trial Info

Start Date :

August 1 2014

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 1 2015

Estimated Enrollment :

146 Patients enrolled

Trial Details

Trial ID

NCT02220920

Start Date

August 1 2014

End Date

July 1 2015

Last Update

January 8 2026

Active Locations (7)

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Page 1 of 2 (7 locations)

1

Reserch site

Chugoku, Japan

2

Reserch site

Chūbu, Japan

3

Reserch site

Hokkaido, Japan

4

Reserch site

Kanto, Japan