A Study of Aleglitazar in Combination With Metformin in Patients With Type 2 Diabetes Mellitus Who Are Inadequately Controlled With Metformin Alone
Completed · Phase 3 · Has a placebo group
Conditions studied: Diabetes Mellitus Type 2
In brief
This multicenter, randomized, double-blind, placebo-controlled study will assess the efficacy, safety and tolerability of aleglitazar plus metformin combination therapy compared with placebo plus metformin in patients with type 2 diabetes mellitus who are inadequately controlled with metformin monotherapy. Patients will be randomized to receive oral doses of 150 mcg aleglitazar once daily or placebo. The anticipated time on study treatment is 26 weeks.
Key facts
- Study ID
- NCT01691846
- Run by
- Hoffmann-La Roche
- People needed
- 200
- Starts
- 2012-10-01
- Expected to finish
- 2013-09-01
- Last updated by the study team
- 2017-02-23
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult patients, >/=18 years of age
- Diagnosis of diabetes mellitus type 2
- Patients treated with stable metformin monotherapy for at least 12 weeks prior to screening
- HbA1c >/=7% and </=9.5% at screening or within 4 weeks prior to screening and at pre-randomization visit
- Fasting plasma glucose </=240 mg/dL at pre-randomization visit
- Agreement to maintain diet and exercise habits during the study
You may not qualify if…
- Patients with Type 1 diabetes mellitus, secondary diabetes, diabetes resulting from pancreatic injury, or acute metabolic diabetic complications within the past 6 months
- Any previous treatment with thiazolidinedione or a dual PPAR agonist
- Any body weight lowering or lipoprotein-modifying therapy within 12 weeks prior to screening (except stable dose of statin)
- Symptomatic congestive heart failure classified as New York Heart Association class II-IV at screening
Where it is running
- Study site — Chino, California, United States
- Study site — Hawaiian Gardens, California, United States
- Study site — Los Angeles, California, United States
- Study site — Santa Ana, California, United States
- Study site — Thousand Oaks, California, United States
- Study site — West Hills, California, United States
- Study site — Kissimmee, Florida, United States
- Study site — Atlanta, Georgia, United States
- Study site — Chicago, Illinois, United States
- Study site — Avon, Indiana, United States
- Study site — Bethesda, Maryland, United States
- Study site — Springfield, Missouri, United States
- Study site — Toms River, New Jersey, United States
- Study site — Altoona, Pennsylvania, United States
- Study site — Beaver, Pennsylvania, United States
- Study site — Morrisville, Pennsylvania, United States
- Study site — Scranton, Pennsylvania, United States
- Study site — Tipton, Pennsylvania, United States
- Study site — Knoxville, Tennessee, United States
- Study site — Dallas, Texas, United States
- Study site — Richmond, Virginia, United States
- Study site — Spokane, Washington, United States
- Study site — Buenos Aires, Argentina
- Study site — Caba, Argentina
- Study site — Rosario, Argentina
Full record on ClinicalTrials.gov
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