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	<title>Pharmaceutical Product Guide &#187; Otsuka Pharmaceutical Co</title>
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		<title>Bristol-Myers&#8217; Abilify To Treat Irritabilty In Pediatric Patients With Autistic Disorder gets FDA Approval</title>
		<link>http://www.pharmaceuticalproductguide.com/blog/2009/12/04/bristol-myers-abilify-to-treat-irritabilty-in-pediatric-patients-with-autistic-disorder-gets-fda-approval/</link>
		<comments>http://www.pharmaceuticalproductguide.com/blog/2009/12/04/bristol-myers-abilify-to-treat-irritabilty-in-pediatric-patients-with-autistic-disorder-gets-fda-approval/#comments</comments>
		<pubDate>Fri, 04 Dec 2009 14:50:51 +0000</pubDate>
		<dc:creator>Kimberly O'Brien</dc:creator>
				<category><![CDATA[Pediatrics]]></category>
		<category><![CDATA[Abilify]]></category>
		<category><![CDATA[Bristol-Myers Squibb Co]]></category>
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		<category><![CDATA[Otsuka Pharmaceutical Co]]></category>
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		<description><![CDATA[Bristol-Myers Squibb Co. and Otsuka Pharmaceutical Co., Ltd. said that FDA has approved the supplemental New Drug Application or sNDA for Abilify for the treatment of irritability associated with autistic disorder in pediatric patients of ages 6 to 17 years. The approval of Abilify for the treatment of irritation in patients with autistic disorder in [...]]]></description>
			<content:encoded><![CDATA[<p><a href="http://www.pharmaceuticalproductguide.com/blog/wp-content/uploads/2009/12/Bristol-Myers-Squibb.png"><img class="alignright size-full wp-image-168" style="margin: 5px" src="http://www.pharmaceuticalproductguide.com/blog/wp-content/uploads/2009/12/Bristol-Myers-Squibb.png" border="0" alt="Bristol Myers Squibb" width="200" height="47" /></a>Bristol-Myers Squibb Co. and Otsuka Pharmaceutical Co., Ltd. said that FDA has approved the supplemental New Drug Application or sNDA for Abilify for the treatment of irritability associated with autistic disorder in pediatric patients of ages 6 to 17 years. The approval of Abilify for the treatment of irritation in patients with autistic disorder in pediatric patients is based on data from two eight-week, randomized, double-blind, placebo-controlled, multi-center, Phase III studies.</p>
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