Clovis Oncology, Inc. is facing a double-hit for its stumbling PARP inhibitor Rubraca (rucaparib), as it has voluntarily withdrawn an indication for third-line ovarian cancer in the US due to safety concerns and is facing a significant delay in the filing timeline for a significant supplemental indication, first-line maintenance therapy in ovarian cancer. The company also appears concerned about ripple effects for the drug’s larger indications.
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Scrip for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?