Supplementary application filed for Cabometyx in first-line renal cell carcinoma

17 August 2017
exelixis-big

The genomics-based drug discovery company Exelixis (Nasdaq: EXEL) has submitted for regulatory approval to market Cabometyx (cabozantinib) in a new indication in the USA.

The Californian firm wants to offer the tyrosine kinase inhibitor to patients with previously untreated advanced renal cell carcinoma (RCC).

It was approved as a second-line therapy for RCC in the USA in April 2016, and in Europe in September of that year, where it is marketed by French drugmaker Ipsen (Euronext: IPN).

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 account

Become a subscriber

 

£820

Or £77 per month

Subscribe Now
  • Unfettered access to industry-leading news, commentary and analysis in pharma and biotech.
  • Updates from clinical trials, conferences, M&A, licensing, financing, regulation, patents & legal, executive appointments, commercial strategy and financial results.
  • Daily roundup of key events in pharma and biotech.
  • Monthly in-depth briefings on Boardroom appointments and M&A news.
  • Choose from a cost-effective annual package or a flexible monthly subscription
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

Company News Directory



Companies featured in this story

More ones to watch >


Today's issue

Company Spotlight





More Features in Pharmaceutical