Drug data last refreshed 2h ago · AI intelligence enriched Yesterday
RUBRACA (rucaparib) is an oral small-molecule PARP inhibitor approved in December 2016 for treatment of ovarian cancer, particularly in patients with BRCA mutations or homologous recombination deficiency. It works by inhibiting poly(ADP-ribose) polymerase, leading to DNA damage accumulation and cell death in cancer cells. The drug represents an important precision medicine option in the poly(ADP-ribose) polymerase inhibitor class.
Product is at peak commercial stage with established market presence; team size likely stable with focus on market penetration and indication expansion rather than launch activities.
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
A Clinical Study Evaluating The Benefit of Adding Rucaparib to Enzalutamide for Men With Metastatic Prostate Cancer That Has Become Resistant To Testosterone-Deprivation Therapy
A Study of Rucaparib and Nivolumab in People With Leiomyosarcoma
A Study of Copanlisib Combined With Rucaparib in Patients With Metastatic Castration-resistant Prostate Cancer
Rucaparib Plus Ramucirumab With or Without Nivolumab in Advanced Gastric and Esophageal Adenocarcinoma
Rucaparib Maintenance Therapy in Advanced Cervical Cancer
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moRUBRACA is an established peak-stage oncology product offering stable, focused career opportunities in commercial execution and patient access roles. Working on this product provides deep expertise in precision medicine, PARP inhibitor mechanisms, and ovarian cancer management, with strategic importance as the team navigates the approaching loss of exclusivity window.