Teetering on the brink, Clovis abandons an early approval for Rubraca
A long suffering Clovis Oncology $CLVS has returned with another setback to report.
The Boulder-based Clovis is using the SEC once again to communicate with shareholders, saying that after a review of their overall survival data from ARIEL4 they’ll be withdrawing an FDA approval from 2016 to market Rubraca as a treatment for third-line BRCA-mutated ovarian cancer. The European approval is also being discarded. The EMA launched its review of that indication in April.
Unlock this article instantly by becoming a free subscriber.
You’ll get access to free articles each month, plus you can customize what newsletters get delivered to your inbox each week, including breaking news.