[A17-36] Baricitinib (rheumatoid arthritis) - Addendum to commission A17-14

Last updated 21.09.2017

Project no.:
A17-36

Commission:
Commission awarded on 08.08.2017 by the Federal Joint Committee (G-BA).

Report type:
Addendum

Status:
Commission completed

Department/Division:
Drug Assessment

Application field:
Muscles, bones and joints

Indication:

Moderate to severe rheumatoid arthritis in adult patients who have responded inadequately to pretreatment

Result of dossier assessment:

Neither advantage nor disadvantage proven from the consideration of the total study population of the JADV study for research questions 2 and 3 of dossier assessment A17-14

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)

A G-BA decision was published.

G-BA documents on this decision

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