Long-term Safety and Tolerability of Alirocumab (SAR236553/REGN727) Versus Placebo on Top of Lipid-Modifying Therapy in High Cardiovascular Risk Patients With Hypercholesterolemia (ODYSSEY Long Term)
Hypercholesterolemia
About this trial
This is an interventional treatment trial for Hypercholesterolemia
Eligibility Criteria
Inclusion criteria:
Either A or B below and who were not adequately controlled with their lipid-modifying therapy:
A) Participants with heterozygous familial hypercholesterolemia (heFH) with or without established coronary heart disease (CHD) or CHD risk equivalents
OR
B) Participants with hypercholesterolemia together with established CHD or CHD risk equivalents.
Exclusion criteria:
- Age < 18 years
- LDL-C <70 mg/dL (< 1.81 mmol/L)
- Fasting serum triglycerides > 400 mg/dL (>4.52 mmol/L)
The above information was not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.
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Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Experimental
Placebo
Alirocumab
Placebo (for alirocumab) every 2 weeks (Q2W) added to stable Lipid-Modifying Therapy (LMT) for 78 weeks.
Alirocumab 150 mg Q2W added to stable LMT for 78 weeks.