[A17-43] Tofacitinib (rheumatoid arthritis) - Addendum to Commission A17-18

Last updated 19.10.2017

Project no.:
A17-43

Commission:
Commission awarded on 04.09.2017 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 with insufficient response to prior treatment

Result of dossier assessment:

For patients ≤ 65 years with unfavourable prognosis pretreated once no hint of lesser benefit versus adalimumab. For 4 questions added benefit therefore 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.

Accompanying information

Further information for consumers and patients is provided on IQWiG's health information website www.informedhealth.org.

Federal Joint Committee (G-BA)

2017-10-19 A G-BA decision was published.

G-BA documents on this decision

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