[A23-38] Upadacitinib (Crohn disease) - Benefit assessment according to §35a Social Code Book V
Last updated 01.08.2023
Project no.:
A23-38
Commission:
Commission awarded on 28.04.2023 by the Federal Joint Committee (G-BA).
Report type:
Dossier assessment
Status:
Commission completed
Department/Division:
Drug Assessment
Topic:
Digestion, metabolism and hormones
Indication:
Adults with moderately to severely active Crohn’s disease
Result of dossier assessment:
- Adults who have had an inadequate response, lost response or were intolerant to conventional therapy: added benefit not proven
- Adults who have had an inadequate response, lost response or were intolerant to a biologic agent (tumour necrosis factor alpha antagonist or integrin inhibitor or interleukin inhibitor): 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.
| Project no. | Title | Status |
|---|---|---|
| A22-92 | Upadacitinib (axial spondyloarthritis) - Benefit assessment according to §35a Social Code Book V | Commission completed |
| A22-91 | Upadacitinib (ulcerative colitis) - Benefit assessment according to §35a Social Code Book V | Commission completed |
| A21-116 | Upadacitinib (atopic dermatitis) - Benefit assessment according to §35a Social Code Book V | Commission completed |
| A21-15 | Upadacitinib (psoriatic arthritis) - Benefit assessment according to §35a Social Code Book V | Commission completed |
| A21-16 | Upadacitinib (ankylosing spondylitis) - Benefit assessment according to §35a Social Code Book V | Commission completed |
| A20-08 | Upadacitinib (rheumatoid arthritis) - Benefit assessment according to §35a Social Code Book V | Commission completed |