AMNOGEvidence Graph
Cases / 2024-03-01-D-1043
discontinued2024-03-01D series

Idecabtagen vicleucel

Neubewertung Orphan > 30 Mio: Multiples Myelom, mind. 3 Vortherapien

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

G-BA action

discontinuation

2024-05-02

Arzneimittel-Richtlinie/Anlage XII: Idecabtagen Vicleucel (Neubewertung eines Orphan Drugs nach Überschreitung der 30 Mio. Euro Grenze; multiples Myelom, mind. 3 Vortherapien) – Einstellung eines Verfahrens zur Nutzenbewertung

Evidence-checked summary

The G-BA issued a discontinuation on 2024-05-02. The official page states that it took effect as follows: 02.05.2024. 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.

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Official case record

What happened, in source order

No inferred stages

Consultation record

Oral hearing and Wortprotokoll

0 hearing

No official oral hearing is attached to this case.

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

2024-05-02

discontinuation

Arzneimittel-Richtlinie/Anlage XII: Idecabtagen Vicleucel (Neubewertung eines Orphan Drugs nach Überschreitung der 30 Mio. Euro Grenze; multiples Myelom, mind. 3 Vortherapien) – Einstellung eines Verfahrens zur Nutzenbewertung

The G-BA issued a discontinuation on 2024-05-02. The official page states that it took effect as follows: 02.05.2024. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.

2 official documents · 3 cited claims

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Official sources

Case document package

3 source
official case pageOfficial G-BA case pageOpen ↗decision textBeschlusstextOpen ↗decision rationaleTragende Gründe zum BeschlussOpen ↗
Generic graph relations · 1
HAS ASSOCIATED DECISIONArzneimittel-Richtlinie/Anlage XII: Idecabtagen Vicleucel (Neubewertung eines Orphan Drugs nach Überschreitung der 30 Mio. Euro Grenze; multiples Myelom, mind. 3 Vortherapien) – Einstellung eines Verfahrens zur Nutzenbewertung