[A22-45] Mepolizumab (hypereosinophilic syndrome) – Addendum to Commission A21-152

Last updated 20.05.2022

Project no.:
A22-45

Commission:
Commission awarded on 12.04.2022 by the Federal Joint Committee (G-BA).

Report type:
Addendum

Status:
Commission completed

Department/Division:
Drug Assessment

Application field:
Haematology

Indication:

Add-on therapy for adult patients with inadequately controlled hypereosinophilic syndrome (HES) without an identifiable non-haematological secondary cause

Result of dossier assessment:

After addendum: Hint of major added benefit

Note:

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.

Federal Joint Committee (G-BA)

2022-05-20 A G-BA decision was published.

G-BA documents on this decision

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