Dossier assessment
Ravulizumab (generalized myasthenia gravis) – Benefit assessment according to § 35a SGB V
Report documents
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Extract of dossier assessment
Ravulizumab (generalized myasthenia gravis) – Benefit assessment according to § 35a SGB V
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Dossier assessment
Ravulizumab (generalized myasthenia gravis) – Benefit assessment according to § 35a SGB V
Dossier assessment
Adults with anti-acetylcholine receptor antibody-positive generalized myasthenia gravis
- Adults who are still eligible for standard treatment: added benefit not proven
- Adults with refractory disease: added benefit not proven
Project details
- Project no.
- A22-115
- Commission
- Commission awarded on 21.10.2022 by the Federal Joint Committee (GBA).
- Report type
- Dossier assessment
- Status
- Commission completed
- Department/Division
- Drug Assessment
- Topic
- Immune system and infections
- Note
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After completion of the assessment by IQWiG the Federal Joint Committee (GBA) 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 GBA website.
The current version 1.1 of the dossier assessment replaces version 1.0 published on 2023-02-01.
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