EMEA grants Lilly's enzastaurin OD status

13 February 2006

The European Medicines Agency (EMEA) has designated US drug major Elil Lilly's oral anticancer agent enzastaurin an Orphan Drug for the treatment of glioblastoma multiforme, a form of primary brain tumor.

The EMEA's opinion, which grants the agent marketing exclusivity benefits and patent extensions, is based on its belief that it could significantly improve patient outcomes. According to Phase II data presented at the annual meeting of the American Society of Clinical Oncology in May 2005, enzastaurin patients with recurrent GM, which is among the most angiogenic of all tumors, experienced a significant tumor response rate with minimal side effects.

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