Promising results for Cephalon's Provigil

13 June 2001

Two new studies have demonstrated that patients given Cephalon'sProvigil (modafinil) tablets, for the treatment of excessive daytime sleepiness associated with narcolepsy, experienced a sustained response for more than 2.5 years. An additional study, in which patients were given either a 200mg or 400mg dose once per day, or a divided 400mg dose, also showed that the response may be related to the dosage. All doses resulted in the patients experiencing significantly improved wakefulness, but those receiving 400mg of Provigil were significantly more awake than the ones receiving 200mg on both the Maintenance of Wakefulness Test and the Clinical Global Impression of Change scale.

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