EU approval for Shire's ADHD drug Intuniv

21 September 2015
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Ireland-based drugmaker Shire (LSE: SHP) saw its shares rise 3.1% to £48.92 in early trading, after the company revealed that the European Commission has granted marketing authorization for its once-daily, non-stimulant Intuniv (guanfacine hydrochloride prolonged release tablets) for the treatment of attention deficit hyperactivity disorder (ADHD) in children and adolescents 6 to 17 years old for whom stimulants are not suitable, not tolerated or have been shown to be ineffective.

The company noted that Intuniv is the first selective alpha-2A adrenergic receptor agonist licensed for the treatment of ADHD in the European Union. Turnover of Intuniv in the second quarter of 2015 plummeted 91% to just $9.5 million because of generic competition in the USA, while sales for ADHD drug Vyvanse (lisdexamfetamine) grew to $424.8 million, up 18% year on year (The Pharma Letter July 23).

Significant advance for patients in Europe

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