[G24-07] Dabrafenib (high-grade malignant glioma in paediatric patients aged 1 year and older, in combination with trametinib) – Assessment according to §35a SGB V (1), Sentence 11
Last updated 01.08.2024
Project no.:
G24-07
Commission:
Commission awarded on 30.04.2024 by the Federal Joint Committee (G-BA).
Report type:
Dossier assessment
Status:
Commission completed
Department/Division:
Health Economics
Topic:
Cancer
In accordance with §35a (1) Sentence 11 Social Code Book (SGB) V, the added medical benefit of orphan drugs is deemed as proven by the fact that they have been approved. On behalf of the Federal Joint Committee (G-BA), IQWiG therefore solely assesses the information on patient numbers and costs in the pharmaceutical company's dossier.
After completion of the assessment by IQWiG the Federal Joint Committee (G-BA) conducts a commenting procedure. The resolution on the extent of added benefit is passed by the G-BA after the hearing. Further information and the decision on the early benefit assessment can be found on the relevant page of the G-BA Website.
https://doi.org/10.60584/G24-08
Project no. | Title | Status |
---|---|---|
A18-59 | Dabrafenib (melanoma) - Benefit assessment according to §35a Social Code Book V | Commission completed |
A17-17 | Dabrafenib (non-small cell lung cancer) - Benefit assessment according to §35a Social Code Book V | Commission completed |
A15-39 | Dabrafenib (new therapeutic indication) - Benefit assessment according to §35a Social Code Book V | Commission completed |
A13-35 | Dabrafenib - Benefit assessment according to § 35a Social Code Book V (dossier assessment) | Commission completed |