NeuroSearch and Abbot intiate Ph II trial of ABT-894

12 March 2007

Scandinavian drugmaker NeuroSearch's development and license partner Abbott has initiated a clinical Phase II study with the drug candidate, ABT-894, for the treatment of attention-deficit hyperactivity disorder in adults. The first patients have been enrolled and dosed in the randomized, double-blind, placebo-controlled, dose-ranging study, which hopes to evaluate the efficacy of ABT-894 for ADHD. The agent is a subtype selective modulator of neuronal nicotinic acetylcholine receptors, which had promising effects in preclinical models for pain and other central and peripheral nervous system diseases, NeuroSearch noted.

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