KOGENATE Bayer (octocog alfa), recombinant human coagulation factor VIII

HAEMATOLOGY - Focus
Opinions on drugs - Posted on Feb 29 2016

Reason for request

Inclusion

In previously untreated patients with a severe haemophilia A, last-line treatment to be used in case of a functional or life-threatening emergency and in the absence of the other available FVIII.

 

  • HELIXATE NexGen and KOGENATE Bayer, identical medicinal products, have Marketing Authorisation in the treatment and prophylaxis of bleeding in patients with haemophilia A (congenital factor VIII deficiency).
  • The efficacy of replacement therapy for haemophilia A using FVIII concentrates may be compromised by the development of inhibitors of FVIII activity, the most serious complication of the treatment.
  • KOGENATE Bayer/HELIXATE NexGen is likely to increase the risk of inhibitors development  compared to other recombinant FVIII in patients with severe, previously untreated, haemophilia A.

Clinical Benefit

Substantial

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Clinical Added Value

no clinical added value

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Therapeutic use

-

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