CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 71 enrolled
Drug / intervention
Canagliflozin (TA-7284) +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02227849
NCT02227849Phase 4Completed

An Open-Label, Multicenter Study to Evaluate the Long-Term Safety, Tolerability and Efficacy of Canagliflozin (TA-7284) as add-on to GLP-1 Analogue in Subjects With Type 2 Diabetes Mellitus

Tanabe Pharma Corporation·interventional·Posted Aug 28, 2014·Updated Jan 8, 2026

In Brief

A Phase 4 clinical trial evaluating Canagliflozin (TA-7284) and GLP-1 analogue for Type 2 Diabetes Mellitus. Completed, enrolled 71 participants across 4 sites.

Detailed Summary

The purpose of this study is to evaluate the safety and efficacy of Canagliflozin (TA-7284) in combination with GLP-1 analogue in patients with type 2 Diabetes for 52 weeks.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesJapan
Collaborators--

Timeline

Phase 4CompletedFinished
201520162017201820192020202120222023202420252026
First PostedAug 28, 2014
Enrollment StartAug 1, 2014
Primary CompletionMar 1, 2016
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 11.8 years ago

Interventions

Canagliflozin (TA-7284)drug

The patients will receive Canagliflozin orally for 52 weeks

GLP-1 analoguedrug