[A21-85] Beclometasone/formoterol/glycopyrronium (asthma) - Addendum to Commission A21-18

Last updated 05.08.2021

Project no.:
A21-85

Commission:
Commission awarded on 22.06.2021 by the Federal Joint Committee (G-BA).

Report type:
Addendum

Status:
Commission completed

Department/Division:
Drug Assessment

Application field:
Airways and respiratory system

Indication:

Adult patients with asthma whose disease is not adequately controlled with a combination of medium- or high-dose ICS and LABA, and who experienced one or more asthma exacerbations in the previous year

Result of dossier assessment:

Unchanged after addendum:

  • Medium-dose ICS/LABA therapy: added benefit not proven.
  • High-dose ICS/LABA therapy: added benefit not proven.
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)

2021-08-05: A G-BA decision was published.

G-BA documents on this decision

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