drugset / Trial / NCT02642159

Efficacy and Safety of Alirocumab Versus Usual Care on Top of Maximally Tolerated Statin Therapy in Patients With Type 2 Diabetes and Mixed Dyslipidemia (ODYSSEY DM-Dyslipidemia)

NCT02642159 ↗

Phase 4 Completed 413 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

Primary Objective: To demonstrate the superiority of alirocumab in comparison with usual care in the reduction of non-high-density lipoprotein cholesterol (non-HDL-C) in participants with type 2 diabetes and mixed dyslipidemia at high cardiovascular risk with non-HDL-C not adequately controlled with maximally tolerated statin therapy. Secondary Objectives: * To demonstrate whether alirocumab is superior in comparison with usual care in its effects on other lipid parameters (ie, low-density lipoprotein cholesterol (LDL-C), apolipoprotein B (Apo B), total cholesterol (Total -C), lipoprotein a (Lp\[a\]), high-density lipoprotein cholesterol (HDL-C), triglycerides (TGs), triglyceride rich lipoproteins (TGRLs), apolipoprotein A-1 (Apo A-1), apolipoprotein C-III (Apo C-III), lipid subfractions by nuclear magnetic resonance (NMR) spectroscopy (ie, LDL-C particle size and LDL, very low-density lipoprotein \[VLDL\], HDL, and intermediate-density lipoprotein \[IDL\] particle number). * To assess changes in glycemic parameters with alirocumab vs. usual care treatment. * To demonstrate the safety and tolerability of alirocumab. * To evaluate treatment acceptance of alirocumab. * To evaluate proprotein convertase subtilisin kexin type 9 (PCSK9) concentrations and antibody development. * To demonstrate the superiority of alirocumab vs. fenofibrate on non-HDL-C and other lipid parameters (subgroup analysis).

Timeline

Start
2016-03-15
Primary completion
2017-03-22
Completion
2017-05-15

Outcome

Met primary endpoint

registry analysis (superiority test); Alirocumab 75 mg Q2W/Up to 150 mg Q2W vs Usual Care; p <0.0001; LS Mean Difference -32.5 (97.5% CI -38.1 to -27.0) NCT02642159 ↗

registry analysis (superiority test); Alirocumab 75 mg Q2W/Up to 150 mg Q2W vs Usual Care: Intent to Prescribe Fenofibrate; p <0.0001; LS Mean Difference -33.3 (97.5% CI -46.6 to -19.9) NCT02642159 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Alirocumab Monoclonal antibody 75 mg Subcutaneous
Subject Alirocumab Monoclonal antibody 150 mg Subcutaneous
Comparator Ezetimibe Unknown — Oral
Comparator Fenofibrate Small molecule — Oral
Comparator Nicotinic acid Unknown — Oral
Comparator Omega-3 fatty acids Unknown — Oral

Indications