Safety and Effectiveness of Evinacumab for the Treatment of Homozygous Familial Hypercholesterolemia
Homozygous Familial Hypercholesterolemia
About this trial
This is an interventional treatment trial for Homozygous Familial Hypercholesterolemia focused on measuring ANGPTL3, Real-life study, Monoclonal antibody
Eligibility Criteria
Inclusion Criteria: HoFH patients having been previously or being currently treated with evinacumab or clinical diagnosis of HoFH requiring additional lipid lowering therapy. Exclusion Criteria: Any new condition or worsening of an existing condition, which in the opinion of the investigator would make the patient unsuitable for enrollment, or could interfere with the patient participating in or completing the study; Pregnant or breastfeeding women; Women of childbearing potential who are unwilling to practice highly effective contraception prior to the initial dose/start of the first treatment, during the study, and for at least 24 weeks after the last dose of study drug.
Sites / Locations
- Ecogene-21
Arms of the Study
Arm 1
Experimental
Evinacumab-treated patients