Cases / 2020-03-01-D-510
completed2020-03-01D series

Tafamidis

Neues Anwendungsgebiet: Amyloidose bei Kardiomyopathie

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Brand
Vyndaqel®
Manufacturer
Pfizer Pharma GmbH

G-BA action

final resolution

2020-08-20

Arzneimittel-​​​Richtlinie/Anlage XII: Tafamidis (neues Anwendungsgebiet: Amyloidose bei Kardiomyopathie)

Evidence-checked summary

The G-BA found a hint of considerable added benefit for Erwachsene Patienten mit Wildtyp- oder hereditärer Transthyretin-Amyloidose mit Kardiomyopathie. The G-BA issued a final resolution on 2020-08-20. 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 4421 →

Patient group

Erwachsene Patienten mit Wildtyp- oder hereditärer Transthyretin-Amyloidose mit Kardiomyopathie

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

2020-07-06

120 parsed turns

Oral hearing: Tafamidis (Neues Anwendungsgebiet: Amyloidose bei Kardiomyopathie)

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

2020-08-20

final resolution

Arzneimittel-​​​Richtlinie/Anlage XII: Tafamidis (neues Anwendungsgebiet: Amyloidose bei Kardiomyopathie)

The G-BA found a hint of considerable added benefit for Erwachsene Patienten mit Wildtyp- oder hereditärer Transthyretin-Amyloidose mit Kardiomyopathie. The G-BA issued a final resolution on 2020-08-20. 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