After 15 years of failure, what can pharma offer Alzheimer's patients?

brain_big

The most recent new treatment for Alzheimer’s disease was approved by European regulators in May 2002, with the US Food and Drug Administration following suit the next year.

Namenda (memantine) represented a novel type of therapy, which offered hope for improved mental function through the regulation of glutamate, a chemical involved in information processing, storage and retrieval.

But as this milestone fast recedes into memory, medical science appears no closer to reaching further breakthroughs, with researchers continuing to disagree over the fundamental causes of the disease, and the most appropriate therapeutic targets.

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

Today's issue

Company Spotlight





More Features in Pharmaceutical