Cases / 2024-01-15-D-1022
completed2024-01-15D series

Pegzilarginase

Hyperargininämie (ARG1-D), ≥ 2 Jahren

Open official case page ↗
Brand
Loargys
Manufacturer
Immedica Pharma Germany GmbH

G-BA action

final resolution

2024-07-04

Arzneimittel-Richtlinie/Anlage XII: Pegzilarginase (Hyperargininämie (ARG1-D), ≥ 2 Jahren)

Evidence-checked summary

The G-BA found a hint of non-quantifiable added benefit for Erwachsene, Jugendliche und Kinder ab 2 Jahren mit Arginase-1-Mangel (Hyperargininämie). The G-BA issued a final resolution on 2024-07-04. The official page states that it took effect as follows: 04.07.2024. 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 6701 →

Patient group

Erwachsene, Jugendliche und Kinder ab 2 Jahren mit Arginase-1-Mangel (Hyperargininämie)

Hint of non quantifiable added benefit

Comparator

Open official result PDF ↗

Official case record

What happened, in source order

No inferred stages

Consultation record

Oral hearing and Wortprotokoll

1 hearing

2024-05-27

112 parsed turns

Oral hearing: Pegzilarginase (Hyperargininämie (ARG1-D), ≥ 2 Jahren)

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

2024-07-04

final resolution

Arzneimittel-Richtlinie/Anlage XII: Pegzilarginase (Hyperargininämie (ARG1-D), ≥ 2 Jahren)

The G-BA found a hint of non-quantifiable added benefit for Erwachsene, Jugendliche und Kinder ab 2 Jahren mit Arginase-1-Mangel (Hyperargininämie). The G-BA issued a final resolution on 2024-07-04. The official page states that it took effect as follows: 04.07.2024. 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

9 source
Generic graph relations · 6