A Phase 3 interventional study of aleglitazar and metformin in Diabetes Mellitus Type 2, sponsored by Hoffmann-La Roche. Completed at 7 sites in 2 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-11-02.
Sponsored by Hoffmann-La Roche · Phase 3, Interventional, and Treatment
This multicenter, randomized, double-blind, placebo-controlled study will evaluate the efficacy, safety and tolerability of aleglitazar in combination with metformin in patients with Type 2 diabetes mellitus who are inadequately controlled with metformin monotherapy. Patients will be randomized to receive either aleglitazar 150 mcg orally daily or placebo for 26 weeks in combination with their pre-existing metformin regimen and dose.
9,589 studies on the registry are indexed under Diabetes Mellitus, Type 2; 1,332 are open to participants now.
This study's enrollment of 7 is below the median of 81 across 7,713 interventional studies indexed under Diabetes Mellitus, Type 2.
Browse Diabetes Mellitus, Type 2 studies →Hoffmann-La Roche is the lead sponsor of 2,099 studies on the registry; 88 are open to participants now.
Of its 324 completed or terminated interventional studies of FDA-regulated products, 245 (76%) have results posted.
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Exclusion Criteria:
Diagnosis or history of:
Drug: aleglitazar · Drug: metformin
Drug: metformin · Drug: placebo
150 mcg orally daily
pre-existing background regimen and dose
matching aleglitazar placebo orally daily
Change in HbA1c
Time frame: from baseline to Week 26
Change in lipids
Time frame: from baseline to Week 26
Change in fasting plasma glucose (FPG)
Time frame: from baseline to Week 26
Responder rates, defined as target HbA1c: < 7.0%, < 6.5% at Week 26
Time frame: 26 weeks
Change in homeostatic index of insulin sensitivity (by HOMA-IS)
Time frame: from baseline to Week 26
Change in homeostatic index of beta cell function (by HOMA-BFC)
Time frame: from baseline to Week 26
Change in markers of insulin sensitivity/cardiovascular risk
Time frame: from baseline to Week 26
Safety: Incidence of adverse events
Time frame: approximately 30 weeks
This study is completed, as verified in Nov 2016. You cannot join it, but the record below documents what was studied.
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Studies of the drug tested here: Aleglitazar