Following non-submission
AWMSG advice |
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Status: Not endorsed (Statement of Advice) | ||
In the absence of a submission from the holder of the marketing authorisation, rucaparib (Rubraca®) cannot be endorsed for use within NHS Wales as monotherapy treatment of adult patients with platinum sensitive, relapsed or progressive, BRCA mutated (germline and/or somatic), high-grade epithelial ovarian, fallopian tube, or primary peritoneal cancer, who have been treated with two or more prior lines of platinum based chemotherapy, and who are unable to tolerate further platinum based chemotherapy. |
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Medicine details |
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Medicine name | rucaparib (Rubraca®) | |
Formulation | 250 mg film-coated tablet, 300 mg film-coated tablet | |
Reference number | 2473 | |
Indication | For use as monotherapy treatment of adult patients with platinum sensitive, relapsed or progressive, BRCA mutated (germline and/or somatic), high-grade epithelial ovarian, fallopian tube, or primary peritoneal cancer, who have been treated with two or more prior lines of platinum based chemotherapy, and who are unable to tolerate further platinum based chemotherapy. |
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Company | Clovis Oncology Inc | |
BNF chapter | Malignant disease & immunosuppression | |
Submission type | Non-submission | |
Status | Not endorsed (Statement of Advice) | |
Ratification by Welsh Government | 02/11/2018 | |
Date of issue | 06/11/2018 |