Cases / 2022-05-01-D-768
completed2022-05-01D series

Tebentafusp

Uveales Melanom, HLA-A*02:01-positiv

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Brand
Kimmtrak
Manufacturer
Immunocore Ireland Ltd.

G-BA action

final resolution

2022-10-20

Arzneimittel-Richtlinie/Anlage XII: Tebentafusp (Uveales Melanom, HLA-A*02:01-positiv)

Evidence-checked summary

The G-BA found a hint of considerable added benefit for Erwachsene mit einem inoperablen oder metastasierten uvealen Melanom und die HLA (humanes Leukozyten-Antigen)-A*02:01-positiv sind. The G-BA issued a final resolution on 2022-10-20. 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 5660 →

Patient group

Erwachsene mit einem inoperablen oder metastasierten uvealen Melanom und die HLA (humanes Leukozyten-Antigen)-A*02:01-positiv sind

Hint of considerable 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

2022-09-05

62 parsed turns

Oral hearing: Tebentafusp (Uveales Melanom, HLA-A*02:01-positiv)

Official Wortprotokoll · 10 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.

G22-15

matched

Tebentafusp (uveal melanoma) - Assessment according to §35a (para. 1., sentence 11) Social Code Book V

Official assessment PDF · 23 pages

G-BA decisions

Distinct actions and documents

1 decision

2022-10-20

final resolution

Arzneimittel-Richtlinie/Anlage XII: Tebentafusp (Uveales Melanom, HLA-A*02:01-positiv)

The G-BA found a hint of considerable added benefit for Erwachsene mit einem inoperablen oder metastasierten uvealen Melanom und die HLA (humanes Leukozyten-Antigen)-A*02:01-positiv sind. The G-BA issued a final resolution on 2022-10-20. 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

7 source
Generic graph relations · 4