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Clinical trial

Safety and Efficacy of Saxagliptin in Triple Therapy to Treat Subjects With Type 2 Diabetes

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Last updated:31st May 2012
Identifier: NCT01619059

The purpose of this study is to learn if BMS-477118 (Saxagliptin) as part of a triple combination therapy can improve (decrease) hemoglobin A1c in patients with type 2 diabetes after 24 weeks of treatment compared to a 2 drug oral antidiabetic therapy. The safety of this treatment will also be studied.


Study Type: Interventional  (Clinical Trial)
Actual Enrollment: 315 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Triple (Participant, Care Provider, Investigator)
Primary Purpose: Treatment
Official Title: A Multicenter, Randomized, Double-Blind, Placebo Controlled, Parallel Group, Phase 3 Trial to Evaluate the Safety and Efficacy of Triple Therapy With Saxagliptin Added to Dapagliflozin in Combination With Metformin Compared to Therapy With Placebo Added to Dapagliflozin in Combination With Metformin in Subjects With Type 2 Diabetes Who Have Inadequate Glycemic Control on Metformin and Dapagliflozin
Study Start Date: June 2012
Actual Primary Completion Date: June 2014
Actual Study Completion Date: January 2015

Arms:
- Experimental:
Arm 1: Saxagliptin+Dapagliflozin+Metformin IR
- Experimental: Arm 2: Placebo+Dapagliflozin+Metformin IR

Category Value
Date last updated at source 2016-04-22
Study type(s) Interventional
Expected enrolment 315
Study start date 2012-06-01
Estimated primary completion date 2014-06-01

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