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rucaparib (Rubraca®)

 

Following non-submission

AWMSG advice

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.

 Statement of Advice (SOA): rucaparib (Rubraca) 2473 (PDF, 98Kb)

Medicine details

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.

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
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