Cases / 2020-07-01-D-556
completed2020-07-01D series

Fostamatinib

Chronische Immunthrombozytopenie

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Brand
Tavlesse®
Manufacturer
Grifols Deutschland GmbH

G-BA action

final resolution

2020-12-17

Arzneimittel-​​​Richtlinie/Anlage XII: Fostamatinib (Chronische Immunthrombozytopenie)

Evidence-checked summary

The G-BA found no proven added benefit for Erwachsene Patienten mit chronischer Immunthrombozytopenie, die refraktär gegenüber anderen Behandlungen sind. The appropriate comparator was Eltrombopag oder Romiplostim. The G-BA issued a final resolution on 2020-12-17. The official page states that it took effect as follows: 17.12.2020. 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 Patienten mit chronischer Immunthrombozytopenie, die refraktär gegenüber anderen Behandlungen sind

Added benefit not proven

Comparator
Eltrombopag oder Romiplostim

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Official case record

What happened, in source order

No inferred stages

Consultation record

Oral hearing and Wortprotokoll

1 hearing

2020-11-09

65 parsed turns

Oral hearing: Fostamatinib (Chronische Immunthrombozytopenie)

Official Wortprotokoll · 13 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.

A20-53

matched

Fostamatinib (chronic immune thrombocytopenia) - Benefit assessment according to §35a Social Code Book V

Official assessment PDF · 31 pages

G-BA decisions

Distinct actions and documents

1 decision

2020-12-17

final resolution

Arzneimittel-​​​Richtlinie/Anlage XII: Fostamatinib (Chronische Immunthrombozytopenie)

The G-BA found no proven added benefit for Erwachsene Patienten mit chronischer Immunthrombozytopenie, die refraktär gegenüber anderen Behandlungen sind. The appropriate comparator was Eltrombopag oder Romiplostim. The G-BA issued a final resolution on 2020-12-17. The official page states that it took effect as follows: 17.12.2020. 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