FERINJECT (ferric carboxymaltose) - Iron deficiency
Opinions on drugs -
Posted on
Mar 08 2024
Reason for request
Indication extension
Key points
Favourable opinion for reimbursement in the treatment of iron deficiency when oral iron preparations are ineffective or cannot be used or there is a clinical need to deliver iron rapidly by the IV route.
Clinical Benefit
Moderate
The Committee deems that the clinical benefit of FERINJECT 50 mg/ml (ferric carboxymaltose) dispersion for injection/infusion is moderate in the treatment of iron deficiency when oral iron preparations are ineffective or cannot be used or there is a clinical need to deliver iron rapidly by the IV route, in patients aged 1 to 13 years.
Clinical Added Value
no clinical added value
Considering:
the results of the randomised, double-blind, phase 3 1VIT17044 study revealing no significant difference compared to oral iron in terms of mean change in Hb levels at D35 compared to baseline (2.22 g/dl versus 1.92 g/dl, p = 0.3108) in children aged 1 to 17 years with iron- deficiency anaemia;
inclusion of a population partially representative of the population targeted by the indication:
only 22% of the patients included in the study were aged 1 to 12 years (25% in the ferric carboxymaltose group) and only 20% of the patients were male;
the study protocol scheduled the inclusion of patients with iron deficiency with anaemia only, whereas the indication also targets patients with iron deficiency without anaemia;
inclusion of patients with a documented history of an episode of inadequate response to all oral iron therapy at least 8 weeks (56 days) prior to randomisation and who responded to oral treatment during the study, raising the hypothesis of poor treatment compliance;
the absence of specific data in children aged 1 to 13 years with haemodialysis-dependent chronic kidney disease;
the absence of data in patients in whom there is a clinical need to deliver iron rapidly;
the lack of long-term efficacy and safety data (follow-up duration of 6 weeks);
the absence of comparative data versus the other injectable iron products;
the Committee deems that FERINJECT 50 mg/ml (ferric carboxymaltose) dispersion for injection/infusion provides no clinical added value (CAV V) in the current care pathway in patients aged 1 to 13 years, which includes the relevant comparators VENOFER (iron hydroxide-sucrose complex) and other injectable iron sucrose products.