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Clinical Trial Results, Litigation Outcomes and Marketing Authorizations - Research Report on Pfizer, GlaxoSmithKline, Sanofi, AstraZeneca, and Neurocrine
Date:9/19/2013

e an important alternative to injectable therapies. The approvals of Lemtrada and Aubagio represent a significant step forward in the way we think about treating this disease," added Hans-Peter Hartung M.D., Ph.D., Professor and Chairman of the Department of Neurology at Heinrich-Heine-University in Duesseldorf, Germany. The Full Research Report on Sanofi SA - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at: [http://www.investorsreports.com/report/2013-09-17/SNY]

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AstraZeneca PLC Research Report

On September 13, 2013, AstraZeneca PLC (AstraZeneca) announced that the US Court of Appeals for the Federal Circuit (Federal Circuit) has issued a temporary injunction against the US launch of the 505(b)2 NDA Esomeprazole Strontium product of Hanmi Pharmaceutical (Hanmi). Previously, in June 2013, AstraZeneca had entered into an agreement with Hanmi and Amneal Pharmaceuticals (Amneal) to streamline litigation issues on the proposed Esomeprazole Strontium and, in July 2013, AstraZeneca had filed a Notice of Appeal for the Federal Circuit, with the Company seeking a reversal of claim construction. According to the release, Hanmi received US FDA approval for Esomeprazole Strontium on August 6, 2013. The Full Research Report on AstraZeneca PLC - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at: [http://www.investorsreports.com/report/2013-09-17/AZN]

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Neurocrine Biosciences, Inc. Research Report

On September 9, 2013, Neurocrine Biosciences, Inc. (Neurocrine) announced Phase IIb results for the 50mg dose of NBI-98854, a small molecule VMAT2 inhibitor in development for tardive dyskinesia. According to the results, the 5
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