Page contentsKey factsDecisionRelated contentTopicsKey facts Invented name Rubraca Active Substance Rucaparib camsylate Therapeutic area Oncology Decision number P/0242/2020 PIP number EMEA-002760-PIP01-19 Pharmaceutical form(s) Film-coated tablet Condition(s) / indication(s) Treatment of fallopian tube cancerTreatment of ovarian cancerTreatment of primary peritoneal cancerTreatment of prostate malignant neoplasms Route(s) of administration Oral use Contact for public enquiries Clovis Oncology Ireland LtdE-mail: regulatoryUK@clovisoncology.comTel. +44(0) 1223 645500 Decision type W: decision granting a waiver in all age groups for all conditions or indications Decision date 22/06/2020DecisionP/0242/2020: EMA decision of 22 June 2020 on the granting of a product specific waiver for rucaparib (camsylate), (EMEA-002760-PIP01-19)AdoptedReference Number: EMA/324759/2020 English (EN) (220.47 KB - PDF)First published: 09/03/2021ViewRelated contentRubracaTopicsPaediatricsShare this page