Cephalon files fentanyl buccal tablet with EMEA

1 April 2007

USA-based biopharmaceutical company Cephalon has filed a marketing application with the European Medicines Agency (EMEA) for its effervescent fentanyl buccal tablet, intended for the management of breakthrough pain during cancer treatment. The product, which was launched in the USA late last year (Marketletter October 2, 2006) under the trade name Fentora, is intended for patients who are already receiving, and are tolerant to, opioid therapy. The Pennsylvania-headquartered firm added that it was also pursuing a clinical development program which would assess the drug in additional indications.

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