aleglitazar
Drug150 mcg orally daily
NCT Number: NCT01871428
This multicenter, randomized, double-blind, placebo-controlled study will evaluate the efficacy, safety and tolerability of aleglitazar monotherapy in patients with Type 2 diabetes mellitus who are drug-naïve to anti-hyperglycemic therapy. Patients will be randomized to receive either aleglitazar 150 mcg orally daily or placebo for 26 weeks.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Chongqing, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
150 mcg orally daily
matching aleglitazar placebo orally daily
Time frame: from baseline to Week 26
Time frame: from baseline to Week 26
Time frame: from baseline to Week 26
Time frame: 26 weeks
Time frame: from baseline to Week 26
Time frame: from baseline to Week 26
Time frame: from baseline to Week 26
Time frame: approximately 30 weeks
Hoffmann-La Roche
Industry
A Multicenter, Randomized, Doubleblind, Placebo-Controlled, Phase III Study to Assess the Efficacy, Safety and Tolerability of Aleglitazar Monotherapy Compared With Placebo in Patients With Type 2 Diabetes Mellitus (T2D) Who Are Drug-Naïve to Antihyperglycemic Therapy
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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