In a filing with the US Securities and Exchange Commission, Clovis Oncology (Nasdaq: CLVS) has revealed it will voluntarily withdraw part of the label for its PARP blocker Rubraca (rucaparib).
The decision relates to a previously-granted approval in BRCA-mutated ovarian cancer, as a later treatment option, after at least two lines of chemotherapy.
The Colorado, USA-based firm has been in discussion with the US Food and Drug Administration around the ARIEL4 post-marketing trial, a requirement of its Accelerated Approval in this indication.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2024 | Headless Content Management with Blaze