[A17-39] Sarilumab (rheumatoid arthritis) – Benefit assessment according to §35a Social Code Book V

Last updated 15.11.2017

Project no.:
A17-39

Commission:
Commission awarded on 15.08.2017 by the Federal Joint Committee (G-BA).

Report type:
Dossier assessment

Status:
Commission completed

Department/Division:
Drug Assessment

Application field:
Muscles, bones and joints

Indication:

Moderate to severe active rheumatoid arthritis

Result of dossier assessment:

Hint of an added benefit for patients for whom treatment with biologic disease-modifying antirheumatic drugs (bDMARD) is indicated for the first time and who do not tolerate MTX. Other patient groups: added benefit not proven

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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