Long-Term Safety Study of Canagliflozin (TA-7284) in Combination With GLP-1 Analogue in Patients With Type 2 Diabetes Mellitus
- Sponsor
- Tanabe Pharma Corporation
- Study ID
- NCT02227849
- Phase
- PHASE4
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 20 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Canagliflozin (TA-7284) — DRUGThe patients will receive Canagliflozin orally for 52 weeks
- GLP-1 analogue — DRUG
Study Details
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.
Key Dates
- Start date
- Aug 31, 2014
- Status verified
- Dec 2025
- Primary completion
- Mar 31, 2016
- Completion
- Mar 31, 2016
Study Design
- Enrollment
- 71 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Canagliflozin (TA-7284) +GLP-1 analogue
Primary Outcome Measure
Safety and Tolerability Assessed by Adverse Events (Number of Participants Experiencing With Adverse Events) [ Time Frame: 52 Weeks ]
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