Study to Evaluate the Efficacy and Safety of Saxagliptin Co-administered With Dapagliflozin in Combination With Metformin Compared to Sitagliptin in Combination With Metformin in Adult Patients With Type 2 Diabetes Who Have Inadequate Glycemic Control on Metformin Therapy Alone

Completed · Phase 3 · Has a placebo group

Conditions studied: Type 2 Diabetes

In brief

Study will evaluate if a combination of saxagliptin and dapagliflozin added concurrently to metformin in combination with diet and exercise is superior to sitagliptin added to metformin in combination with diet and exercise in reducing mean HbA1c over a treatment period of 26 weeks.

Key facts

Study ID

NCT02284893

Run by

AstraZeneca

People needed

461

Starts

2014-09-09

Expected to finish

2016-09-20

Last updated by the study team

2018-06-01

Who can join

Age: 18 and older, up to 120. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with Type 2 diabetes mellitus (T2DM) with inadequate glycemic control, defined as a central laboratory glycosylated hemoglobin (HbA1c) ≥8.0% and ≤ 10.5 % obtained at the screening visit
• Subjects should have been taking the same daily dose of metformin ≥ 1500 mg for at least 8 weeks prior to the enrollment visit and with no intake of other antihyperglycemic therapy for more than 14 days (consecutive or not) during 12 weeks prior to screening
• BMI > 20.0 kg/m2 at the enrollment visit
• Males and Females, age ≥18 years old at time of screening visit
• Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of HCG) within 24 hours prior to the start of study drug
• Women must not be breastfeeding

You may not qualify if…

• Clinically diagnosed with Type I diabetes, known diagnosis of Maturity Onset Diabetes of Young (MODY), secondary diabetes mellitus or diabetes insipidus
• History of diabetic ketoacidosis
• Any of the following cardiovascular (CV)/Vascular Diseases within 3 months of the enrollment visit
• Myocardial infarction
• Cardiac surgery or revascularization (coronary artery bypass surgery Coronary Artery Bypass Graft [(CABG)]/percutaneous transluminal coronary angioplasty percutaneous transluminal coronary angioplasty [(PTCA)])
• Unstable angina
• Unstable congestive heart failure (CHF)
• Transient ischemic attack (TIA) or significant cerebrovascular disease
• Unstable or previously undiagnosed arrhythmia
• Congestive heart failure, defined as New York Heart Association (NYHA) Class III and IV, unstable or acute congestive heart failure and/or known left ventricular ejection fraction of ≤ 40%
• Renal Disease
• Hepatic Diseases
• Hematological and Oncological Disease/Conditions
• Hemoglobin ≤ 11.0 g/dL (110 g/L) for men; hemoglobin ≤ 10.0 g/dL (100 g/L) for women
• Abnormal Free T4

Where it is running

• Research Site — Mesa, Arizona, United States
• Research Site — Phoenix, Arizona, United States
• Research Site — Little Rock, Arkansas, United States
• Research Site — Huntington Beach, California, United States
• Research Site — Huntington Park, California, United States
• Research Site — Lomita, California, United States
• Research Site — Los Angeles, California, United States
• Research Site — Northridge, California, United States
• Research Site — Norwalk, California, United States
• Research Site — Paramount, California, United States
• Research Site — Sacramento, California, United States
• Research Site — Tarzana, California, United States
• Research Site — Tustin, California, United States
• Research Site — Golden, Colorado, United States
• Research Site — Coral Gables, Florida, United States
• Research Site — Kissimmee, Florida, United States
• Research Site — Miami, Florida, United States
• Research Site — Miami, Florida, United States
• Research Site — Miami, Florida, United States
• Research Site — Miami Beach, Florida, United States
• Research Site — Palm Harbor, Florida, United States
• Research Site — Pembroke Pines, Florida, United States
• Research Site — Chicago, Illinois, United States
• Research Site — Council Bluffs, Iowa, United States
• Research Site — Mesa, Arizona, United States

Full record on ClinicalTrials.gov

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