Sciele Pharma and Addrenex Pharmaceuticals have initiated patient enrollment for Phase III clinical trials of Clonicel in the US for the treatment of attention deficit and hyperactivity disorder in children.
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In July 2007, Sciele signed an exclusive licensing agreement with Addrenex to market a sustained-release formulation of clonidine hydrochloride for the treatment of attention deficit and hyperactivity disorder (ADHD) and hypertension.
Moise Khayrallah, CEO of Addrenex, said: “We are excited about the benefits Clonicel may provide children between the ages of 6 and 17 who have ADHD. This is the first Phase III clinical trial that is being conducted using a new formulation of clonidine for the treatment of ADHD. Clonicel is a 12-hour, sustained-release formulation, which is designed to reduce the side effects of clonidine.”
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