[A21-15] Upadacitinib (psoriatic arthritis) - Benefit assessment according to §35a Social Code Book V

Last updated 15.07.2021

Project no.:
A21-15

Commission:
Commission awarded on 01.03.2021 by the Federal Joint Committee (G-BA).

Report type:
Dossier assessment

Status:
Commission completed

Department/Division:
Drug Assessment

Topic:
Muscles, bones and joints

Indication:

Adult patients with active psoriatic arthritis

Result of dossier assessment:

Patients who have had an inadequate response or who have been intolerant to a prior disease-modifying antirheumatic drug (DMARD) therapy: hint of minor added benefit. Patients who have had an inadequate response or who have been intolerant to a prior therapy with biologic disease-modifying antirheumatic drugs (bDMARDs): 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.

Federal Joint Committee (G-BA)

2021.07.15 A G-BA decision was published.

G-BA documents on this decision

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