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Home » Newsletters » BioWorld Science

BioWorld Science

Sep. 13, 2013

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Identification of a plasma biomarker to assess resistant GVHD

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Novel M4 receptor modulators presented by The Vanderbilt University

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Amicus Therapeutics collaborates with Biogen Idec for Parkinson's disease drugs

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Eliglustat noninferior to imiglucerase in phase III ENCORE study

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Phase IIb AllerT birch pollen allergy vaccine study meets primary endpoint

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SMT-19969 shows selective activity against C. difficile infection

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Antisense oligonucleotides synergistically inhibit prostate cancer cell growth in vitro and in vivo

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Amgen presents novel GPR119 agonists at ACS meeting

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Dainippon Sumitomo Pharma reports discovery of glucagon receptor antagonists

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Kakeromycin may represent a new class of antifungals

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Wayne State University discloses new gene constructs for cancer

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First patient treated in Neuralstem's phase II trial in ALS

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Roche acquires license to Inovio's DNA-based prostate cancer and hepatitis B vaccine candidates

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ChemoCentryx reports interim data for CCX-140 in patients with diabetic nephropathy

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Actelion to initiate phase III program of cadazolid for CDAD

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FCGR3A gene and its association with sarcoidosis

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RedHill Biopharma's RHB-104 shows potential for treatment of lupus

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ALS Therapy Development Institute and Anida Pharma form partnership

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Theraclone Sciences begins phase IIa trial of TCN-202 for prevention of CMV

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FDA grants breakthrough therapy designation to entinostat in advanced breast cancer

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Janssen Biotech initiates phase II study of daratumumab in multiple myeloma

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Dosing begins in phase II trial of Conatus' emricasan in severe alcoholic hepatitis

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Verastem commences phase II trial of defactinib in mesothelioma

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Exelixis begins CELESTIAL phase III trial of cabozantinib

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Italian group discloses novel GSK-3 beta inhibitors

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FDA committee recommends accelerated approval of new indication for Genentech's Perjeta

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FDA grants fast track designation to Synta's ganetespib in non-small cell lung adenocarcinoma

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Sanofi withdraws lixisenatide NDA in the U.S.

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