Shire says ADHD drug meets main goal of study

Published On 2016-07-02 10:25 GMT   |   Update On 2016-07-02 10:25 GMT

Irish drugmaker Shire Plc said a study testing an experimental drug to treat attention-deficit disorder met the main goal, bringing the drug one step closer to approval in the United States.


The company's shares were up 3 percent at 4381 pence at 12.52 GMT on the London Stock Exchange. Shire's U.S. listed shares were up 3 percent at $176.28 in light premarket trading on the Nasdaq.


Shire, which sells Vyvanse and Intuniv to treat Attention-deficit/Hyperactivity Disorder (ADHD), has focused on developing treatments for the condition that affects about 4 percent of the U.S. population.


Data showed both doses of the experimental drug, SHP465, were better than a placebo in treating patients with Attention-deficit/Hyperactivity Disorder, Shire said.


Shire, which sponsored an awareness campaign on ADHD that included Maroon 5 singer Adam Levine in 2011, said if SHP465 was approved by the FDA, the company's ADHD drug franchise would be protected up to 2029.


The company said it was on track to get the drug approved by the U.S. Food and Drug Administration in the second half of 2017.


Shire, which is still integrating its acquisition of Baxalta, had reported in April similar results from a late-stage safety and efficacy study.

Article Source : Reuters

Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2020 Minerva Medical Treatment Pvt Ltd

Our comments section is governed by our Comments Policy . By posting comments at Medical Dialogues you automatically agree with our Comments Policy , Terms And Conditions and Privacy Policy .

Similar News