CV Therapeutics' Ranexa get FDA OK

6 February 2006

California, USA-based CV Therapeutics says that the Food and Drug Administration has approved Ranexa (ranolazine extended-release tablets) for the treatment of chronic angina. The FDA approval document contains the caveat the drug be reserved for patients who have not achieved an adequate response to other compounds during the course of their treatment.

The regulatory clearance marks the first new pharmaceutical approach to treat angina in more than 20 years, notes the firm, adding that it intends to make the product available across the USA in late March.

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





Today's issue

Company Spotlight