Cases / 2025-03-01-D-1168
completed2025-03-01D series

Fedratinib

Neubewertung nach Fristablauf: Myelofibrose

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

G-BA action

final resolution

2025-08-21

Arzneimittel-Richtlinie/Anlage XII: Fedratinib (Neubewertung nach Fristablauf: Myelofibrose)

Evidence-checked summary

The G-BA issued a final resolution on 2025-08-21. The official page states that it took effect as follows: 21.08.2025. 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

2025-07-07

48 parsed turns

Oral hearing: Fedratinib (Neubewertung nach Fristablauf: Myelofibrose)

Official Wortprotokoll · 10 pages

IQWiG comparison

Assessment record versus G-BA action

0 reference

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

No IQWiG assessment reference is present on the validated official case page. This is an explicit absence, not a broken graph link.

G-BA decisions

Distinct actions and documents

1 decision

2025-08-21

final resolution

Arzneimittel-Richtlinie/Anlage XII: Fedratinib (Neubewertung nach Fristablauf: Myelofibrose)

The G-BA issued a final resolution on 2025-08-21. The official page states that it took effect as follows: 21.08.2025. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.

4 official documents · 3 cited claims

Official sources

Case document package

9 source
Generic graph relations · 6