Cases / 2023-10-01-D-975
completed2023-10-01D series

Pegunigalsidase alfa

Morbus Fabry

Open official case page ↗
Brand
Elfabrio
Manufacturer
Chiesi GmbH

G-BA action

final resolution

2024-03-21

Arzneimittel-Richtlinie/Anlage XII: Pegunigalsidase alfa (Morbus Fabry)

Evidence-checked summary

The G-BA found no proven added benefit for Erwachsene mit bestätigter Morbus-Fabry-Diagnose (α Galaktosidase-A-Mangel). The appropriate comparator was Agalsidase alfa oder Agalsidase beta oder Migalastat (nur für Patientinnen und Patienten mit einer auf die Behandlung ansprechenden Mutation). The G-BA issued a final resolution on 2024-03-21. The official page states that it took effect as follows: 21.03.2024. 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.

Final benefit result

G-BA result by patient group

Open decision 6511 →

Patient group

Erwachsene mit bestätigter Morbus-Fabry-Diagnose (α Galaktosidase-A-Mangel)

Added benefit not proven

Comparator
Agalsidase alfa oder Agalsidase beta oder Migalastat (nur für Patientinnen und Patienten mit einer auf die Behandlung ansprechenden Mutation)

Open official result PDF ↗

Official case record

What happened, in source order

No inferred stages

Consultation record

Oral hearing and Wortprotokoll

1 hearing

2024-02-05

94 parsed turns

Oral hearing: Pegunigalsidase alfa (Morbus Fabry)

Official Wortprotokoll · 14 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.

A23-95

matched

Pegunigalsidase alfa (Fabry disease) – Benefit assessment according to §35a Social Code Book V

Official assessment PDF · 76 pages

G-BA decisions

Distinct actions and documents

1 decision

2024-03-21

final resolution

Arzneimittel-Richtlinie/Anlage XII: Pegunigalsidase alfa (Morbus Fabry)

The G-BA found no proven added benefit for Erwachsene mit bestätigter Morbus-Fabry-Diagnose (α Galaktosidase-A-Mangel). The appropriate comparator was Agalsidase alfa oder Agalsidase beta oder Migalastat (nur für Patientinnen und Patienten mit einer auf die Behandlung ansprechenden Mutation). The G-BA issued a final resolution on 2024-03-21. The official page states that it took effect as follows: 21.03.2024. The page lists Arzneimittel-Richtlinie, Anlage XII: Nutzenbewertung nach § 35a SGB V as the normative target.

2 official documents · 4 cited claims

Official sources

Case document package

8 source
Generic graph relations · 6