EMA to review Shire application for blood disorder therapy

22 June 2017
2019_biotech_test_vial_discovery_big

The European Medicines Agency has agreed to review London-listed Shire’s (LSE: SHP) application for approval to market Veyvondi (von Willebrand factor) as a treatment for von Willebrand Disease (VWD), the most common inherited bleeding disorder.

The therapy was approved in the USA in December 2015, where it is marketed as Vonvendi.

VWD is the most common inherited bleeding disorder worldwide, affecting up to 1% of the world’s population. It is caused by a deficiency or dysfunction of von Willebrand factor, resulting in impaired blood clotting.

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

Companies featured in this story

More ones to watch >


Today's issue

Company Spotlight





More Features in Biotechnology