[A18-32] Rurioctocog alfa pegol (haemophilia A) - Benefit assessment according to §35a Social Code Book V

Last updated 15.08.2018

Project no.:
A18-32

Commission:
Commission awarded on 16.05.2018 by the Federal Joint Committee (G-BA).

Report type:
Dossier assessment

Status:
Commission completed

Department/Division:
Drug Assessment

Application field:
Haematology

Indication/Intervention:

Treatment and prophylaxis of bleeding in patients with haemophilia A (congenital factor VIII deficiency) aged 12 years or older

Result of dossier assessment:

No study data; added benefit not proven in comparison with the appropriate comparator therapy

Note:

After completion of the assessment by IQWiG the Federal Joint Committee (G-BA) conducts a commenting procedure. This may provide supplementary information and as a result lead to a modified benefit assessment. Further information and the decision on the early benefit assessment can be found on the relevant page of the G-BA website.

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Further information for consumers and patients is provided on IQWiG's health information website www.informedhealth.org.

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