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

Last updated 16.09.2021

Project no.:

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

Report type:

Commission completed

Drug Assessment

Application field:


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.


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)

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

G-BA documents on this decision


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