[G15-02] Ramucirumab - Assessment according to §35a (para. 1., sentence 10) Social Code Book V (dossier assessment)
Last updated 04.05.2015
Project no.:
G15-02
Commission:
Commission awarded on 27.01.2015 by the Federal Joint Committee (G-BA).
Report type:
Dossier assessment
Status:
Commission completed
Department/Division:
Health Economics
Application field:
Cancer
In accordance with § 35a (para. 1, sentence 10) Social Code Book V, the added medical benefit of orphan drugs is deemed as proven by the fact that they have been approved. For the Ramucirumab report commissioned by 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. This may provide supplementary information and as a result lead to a modified benefit assessment. Further information and the decision on the early benefit assessment can be found on the relevant page of the G-BA website.
Project no. | Title | Status |
---|---|---|
A20-13 | Ramucirumab (NSCLC, combination with erlotinib) - Benefit assessment according to §35a Social Code Book V | Commission completed |
A19-73 | Ramucirumab (hepatocellular carcinoma) - Benefit assessment according to §35a Social Code Book V | Commission completed |
A16-23 | Ramucirumab - Benefit assessment according to §35a Social Code Book V | Commission completed |
A16-11 | Ramucirumab (new therapeutic indication) - Benefit assessment according to §35a Social Code Book V | Commission completed |
A16-10 | Ramucirumab (new therapeutic indication) - Benefit assessment according to §35a Social Code Book V | Commission completed |
Federal Joint Committee (G-BA)
2015-07-16 A G-BA decision was published.