Cases / 2025-12-15-D-1280
completed2025-12-15D series

Nivolumab

Neubewertung nach Fristablauf: Urothelkarzinom, PD-L1-Expression ≥ 1 %, adjuvante Therapie

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Brand
Opdivo
Manufacturer
Bristol-Myers Squibb GmbH & Co. KGaA

G-BA action

final resolution

2026-06-04

Arzneimittel-​​​Richtlinie/Anlage XII: Nivolumab (Neubewertung nach Fristablauf: Urothelkarzinom, PD-L1-Expression ≥ 1 %, adjuvante Therapie)

Evidence-checked summary

The G-BA issued a final resolution on 2026-06-04. The official page states that it took effect as follows: 04.06.2026. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.

This is the latest validated public action attached to this case. It is separate from the IQWiG assessment result.

Official case record

What happened, in source order

No inferred stages

Consultation record

Oral hearing and Wortprotokoll

1 hearing

2026-04-27

53 parsed turns

Oral hearing: Nivolumab (Neubewertung nach Fristablauf: Urothelkarzinom, PD-L1-Expression ≥ 1 %, adjuvante Therapie)

Official Wortprotokoll · 11 pages

IQWiG comparison

Assessment record versus G-BA action

1 reference

IQWiG assessment findings and the later G-BA action are separate records. Open both to compare them.

A25-154

matched

Nivolumab (urothelial carcinoma, adjuvant) – Benefit assessment according to §35a Social Code Book V (expiry of the decision)

Official assessment PDF · 138 pages

G-BA decisions

Distinct actions and documents

1 decision

2026-06-04

final resolution

Arzneimittel-​​​Richtlinie/Anlage XII: Nivolumab (Neubewertung nach Fristablauf: Urothelkarzinom, PD-L1-Expression ≥ 1 %, adjuvante Therapie)

The G-BA issued a final resolution on 2026-06-04. The official page states that it took effect as follows: 04.06.2026. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.

2 official documents · 3 cited claims

Official sources

Case document package

7 source
Generic graph relations · 5