EVKEEZA (evinacumab) - Paediatric patients aged 6 months to 4 years with homozygous familial hypercholesterolaemia (HoFH)

Opinions on drugs - Posted on Sep 10 2025

Reason for request

Modification of the listing conditions

Summary of opinion

Favourable opinion for reimbursement of EVKEEZA (evinacumab) as an adjunct to diet and other low-density lipoprotein-cholesterol (LDL-C) lowering therapies for the treatment of paediatric patients aged 6 months to 4 years with homozygous familial hypercholesterolaemia (HoFH).


Clinical Benefit

Moderate

The clinical benefit of EVKEEZA (evinacumab) 150 mg/ml concentrate for solution for infusion is substantial in the MA indication.


Clinical Added Value

minor

Considering:

  • the absence of clinical study data for the paediatric population under 5 years of age;
  • the data previously submitted and analysed concerning the other populations for which evinacumab is indicated (children aged 5 to 11 years [non-comparative CL-17100 study and extrapolation data] and adults and adolescents [comparative ELIPSE-HoFH study]);
  • reassuring use data from compassionate access programmes in children under 5 years of age and an extrapolation analysis of the efficacy of evinacumab in this population based on a pharmacokinetics (PK) and PK/PD (pharmacodynamics) simulation model;
  • the absence of any new safety signals and the relatively favourable safety profile of evinacumab;

the Committee deems that EVKEEZA (evinacumab) 150 mg/ml concentrate for solution for infusion provides a minor clinical added value (CAV IV) in the current care pathway for the treatment of children aged 6 months to 4 years with homozygous familial hyper-cholesterolaemia.


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