Cases / 2020-11-01-D-588
completed2020-11-01D series

Burosumab

Neues Anwendungsgebiet: X-chromosomale Hypophosphatämie, ≥ 18 Jahre

Open official case page ↗
Brand
Crysvita
Manufacturer
Kyowa Kirin GmbH

G-BA action

final resolution

2021-04-15

Arzneimittel-Richtlinie/Anlage XII: Burosumab (Neues Anwendungsgebiet: X-chromosomale Hypophosphatämie, ≥ 18 Jahre)

Evidence-checked summary

The G-BA found a hint of minor added benefit for Erwachsene Patienten mit X-chromosomaler Hypophosphatämie (XLH). The G-BA issued a final resolution on 2021-04-15. 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

Open decision 4784 →

Patient group

Erwachsene Patienten mit X-chromosomaler Hypophosphatämie (XLH)

Hint of minor 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

2021-03-09

107 parsed turns

Oral hearing: Burosumab (Neues Anwendungsgebiet: X-chromosomale Hypophosphatämie, ≥ 18 Jahre)

Official Wortprotokoll · 19 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

2021-04-15

final resolution

Arzneimittel-Richtlinie/Anlage XII: Burosumab (Neues Anwendungsgebiet: X-chromosomale Hypophosphatämie, ≥ 18 Jahre)

The G-BA found a hint of minor added benefit for Erwachsene Patienten mit X-chromosomaler Hypophosphatämie (XLH). The G-BA issued a final resolution on 2021-04-15. 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