EC orphan status for Fovea's RdCVF

14 January 2008

Paris, France-based Fovea Pharmaceuticals SA, which last December raised $44.0 million in a series B financing, has announced that its product, recombinant human rod-derived cone viability factor (rh-RdCVF), has been designated as Orphan Medicinal Product by the European Commission. This follows the positive opinion from the European Medicines Agency's (EMEA) Committee for Orphan Medicinal Products (COMP) for the treatment of retinitis pigmentosa, a genetic disease leading to progressive loss of vision. Fovea is currently conducting preclinical studies of RdCVF and has demonstrated efficacy in an animal model of the disease.

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 Spotlight