Study identifier:CV181-057
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Multicenter, Randomized, Double-Blind, Phase 3 Trial to Evaluate the Efficacy and Safety of Saxagliptin Added to Insulin Monotherapy or to Insulin in Combination With Metformin in Subjects With Type 2 Diabetes Who Have Inadequate Glycemic Control on Insulin Alone or on Insulin in Combination With Metformin
Type 2 Diabetes
Phase 3
No
Saxagliptin, 5 mg + insulin, Placebo + insulin
All
455
Interventional
18 Years - 78 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 May 2015 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
AstraZeneca
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: Saxagliptin, 5 mg + insulin Saxagliptin, 5 mg, plus insulin, administered to participants with Type 2 diabetes inadequately controlled with insulin alone or with insulin plus metformin | Drug: Saxagliptin, 5 mg + insulin Saxagliptin, 5-mg tablets (plus stable insulin dose), given orally once daily (24 weeks short-term, 28 weeks long-term); participants stratified by use of stable metformin dose; flexible insulin dose (as needed for rescue) Other Name: BMS-477118 |
Placebo Comparator: Placebo + insulin Placebo administered to participants with Type 2 diabetes inadequately controlled with insulin alone or with insulin plus metformin | Drug: Placebo + insulin Placebo tablets given orally once daily for 24 weeks (short-term period)+ insulin with metformin |