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Acquisitions, Clinical Trial Results, Date Extensions and Financial Results - Research Report on Endo, Astex, Auxilium, Accuray, and BioScrip
Date:9/2/2013

: [http://www.investorsreports.com/report/2013-08-28/ENDP]

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Astex Pharmaceuticals, Inc. Research Report

On August 28, 2013, Astex Pharmaceuticals, Inc. (Astex) reported topline results from the ongoing Phase 2 trial of SGI-110 in patients with AML and MDS. The Company stated that as of the end of the June 2013 data cutoff, 67 AML patients had a minimum follow up of 3 months (50 patients representing the complete cohort of relapsed/refractory AML, and 17 patients in the treatment-naïve elderly AML not suitable for induction chemotherapy cohort). According to Astex, the primary endpoint was overall remission rate (Complete Remission or CR Complete Remission with Incomplete hematologic recovery or CRi/CRp), and there were 8 remissions in relapsed/refractory AML and 9 remissions in treatment-naïve elderly AML for an overall complete remission rate of (CR, CRi/CRP0 of 17/67) or 25%. The Full Research Report on Astex Pharmaceuticals, Inc. - including full detailed breakdown, analyst ratings and price targets - is available to download free of charge at: [http://www.investorsreports.com/report/2013-08-28/ASTX]

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Auxilium Pharmaceuticals, Inc. Research Report

On August 28, 2013, Auxilium Pharmaceuticals, Inc. (Auxilium) announced that the U.S. Food and Drug Administration (FDA) has notified the Company that it is extending the Prescription Drug Fee User Act (PDUFA) goal date for the Company's supplemental biologics license application (sBLA) for XIAFLEX (collagenase clostridium histolyticum) for the treatment of Peyronie's disease (PD) from September 6, 2013 to December 6, 2013. Commenting on the extension, Adrian Adams, CEO and President of Auxilium Pharmaceuticals, said, "While we are disappointed in any delay of approval, we remain confident in the XIAF
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