Phase IV study with a 36-week extension period to evaluate the efficacy and safety of dapagliflozin therapy when added to the therapy of Japanese patients with type 2 diabetes with inadequate glycemic control on insulin.

Study identifier:D1692C00013

ClinicalTrials.gov identifier:NCT02157298

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

A 16-week multicenter, randomized, parallel-group, double-blind, placebo-controlled Phase IV study with a 36-week extension period to evaluate the efficacy and safety of dapagliflozin therapy when added to the therapy of Japanese patients with type 2 diabetes with inadequate glycemic control on insulin

Medical condition

Type 2 Diabetes Mellitus

Phase

Phase 4

Healthy volunteers

No

Study drug

Dapagliflozin 5 mg, Placebo tablet

Sex

All

Actual Enrollment

266

Study type

Interventional

Age

20 Years - 130 Years

Date

Study Start Date: 01 Jun 2014
Primary Completion Date: 01 Feb 2015
Study Completion Date: 01 Nov 2015

Study design

Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment

Verification:

Verified 01 Mar 2016 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria