Shire's guanfacine hydrochloride extended release reduces core ADHD symptoms in Phase III trial

10 December 2014
shire-logo-big

Ireland-headquartered drugmaker Shire (LSE: SHP) has achieved positive results in a Phase III trial of guanfacine hydrochloride extended release (GXR) in attention-deficit/hyperactivity disorder in children and adolescents.

The drug shows a significant reduction in ADHD core symptoms and global functioning.

The Phase III study assessed the efficacy and safety of once-daily dose-optimized GXR in children and adolescents aged 6-17 years old with moderate-to-severe ADHD in a placebo-controlled trial.

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





More Features in Pharmaceutical