Cases / 2022-09-01-D-858
completed2022-09-01D series

Efgartigimod alfa

Myasthenia gravis, AChR-Antikörper+

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Brand
Vyvgart
Manufacturer
Argenx Germany GmbH

G-BA action

final resolution

2023-02-16

Arzneimittel-Richtlinie/Anlage XII: Efgartigimod alfa (Myasthenia gravis, AChR-Antikörper+)

Evidence-checked summary

The G-BA found a hint of considerable added benefit for Erwachsene mit generalisierter Myasthenia gravis, die Anti-Acetylcholin-Rezeptor -Antikörper positiv sind. The G-BA issued a final resolution on 2023-02-16. The official page states that it took effect as follows: aufgehoben. 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.

Final benefit result

G-BA result by patient group

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Patient group

Erwachsene mit generalisierter Myasthenia gravis, die Anti-Acetylcholin-Rezeptor -Antikörper positiv sind

Hint of considerable added benefit

Comparator

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Official case record

What happened, in source order

No inferred stages

Consultation record

Oral hearing and Wortprotokoll

1 hearing

2023-01-09

100 parsed turns

Oral hearing: Efgartigimod alfa (Myasthenia gravis, AChR-Antikörper+)

Official Wortprotokoll · 15 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

2023-02-16

final resolution

Arzneimittel-Richtlinie/Anlage XII: Efgartigimod alfa (Myasthenia gravis, AChR-Antikörper+)

The G-BA found a hint of considerable added benefit for Erwachsene mit generalisierter Myasthenia gravis, die Anti-Acetylcholin-Rezeptor -Antikörper positiv sind. The G-BA issued a final resolution on 2023-02-16. The official page states that it took effect as follows: aufgehoben. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.

3 official documents · 4 cited claims

Official sources

Case document package

8 source
Generic graph relations · 5