[A24-21] Pegunigalsidase alfa (Fabry disease) – Addendum to Project A23-95
Last updated 21.03.2024
Project no.:
A24-21
Commission:
Commission awarded on 06.03.2024 by the Federal Joint Committee (G-BA).
Report type:
Addendum
Status:
Commission completed
Department/Division:
Drug Assessment
Topic:
Digestion, metabolism and hormones
Adult patients with a confirmed diagnosis of Fabry disease (deficiency of alpha-galactosidase)
Unchanged after addendum: added benefit not proven
If the need for additional work on a project commissioned by the G-BA arises during consultations, then IQWiG presents a report in the form of an "addendum". The G-BA subsequently decides on the extent of the added benefit, thus completing the early benefit assessment.
https://dx.doi.org/10.60584/A24-21_en
| Project no. | Title | Status |
|---|---|---|
| A23-95 | Pegunigalsidase alfa (Fabry disease) – Benefit assessment according to §35a Social Code Book V | Commission completed |
Federal Joint Committee (G-BA)
2024-03-21 A G-BA decision was published.