[A21-106] Nivolumab (melanoma, adjuvant) - Addendum to Commission A21-39

Last updated 16.09.2021

Project no.:
A21-106

Commission:
Commission awarded on 10.08.2021 by the Federal Joint Committee (G-BA).

Report type:
Addendum

Status:
Commission completed

Department/Division:
Drug Assessment

Application field:
Cancer

Indication:

Adjuvant treatment of adults with melanoma with involvement of lymph nodes or metastatic disease who have undergone complete resection

Result of dossier assessment:

Unchanged after addendum:

  • Stage IIIB/C and IV disease: hint of non-quantifiable added benefit.
  • Stage IIIA disease: 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)

2021-09-16 A G-BA decision was published.

G-BA documents on this decision

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