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CHMP of EMA conveyed negative trend vote of Puma’s MA for neratinib for treating HER2-positive…

Jan 24, 2018
Puma Biotechnology asserted that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has conveyed a negative trend vote after discussions…
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Cerus affirms positive results for Phase 3 transfusion study assessing INTERCEPT RBC’s in…

Jan 24, 2018
Cerus Corporation asserted successful achievement of primary efficacy and safety endpoints in the Company's Phase 3 transfusion study of Chronic anaemia assessing INTERCEPT-treated Red…
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Tabuk Pharmaceuticals enters into licensing and supply agreement with red otc development GmbH

Jan 23, 2018
One of the leading pharmaceutical companies in the Middle East and North Africa region, Tabuk Pharmaceuticals enters into licensing and supply agreement with red otc development GmbH on…
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Deborah Dunsire, MD appointed by Alexion to its Board of Directors

Jan 23, 2018
Alexion Pharmaceuticals, confirmed that Deborah Dunsire, MD has been appointed to its Board of Directors as a new independent director. Dr. Dunsire served as President and Chief…
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Celgene and Juno Therapeutics sign definitive merger agreement

Jan 23, 2018
Celgene Corporation and Juno Therapeutics signed a definitive merger agreement in which Celgene has initiated acquisition of Juno Therapeutics. As per the terms of the agreement, …
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Seattle Genetics asserted EC’s extension of marketing authorization for ADCETRIS

Jan 23, 2018
Seattle Genetics confirmed that its collaborator, Takeda Pharmaceutical Company Limited has asserted the fact that European Commission has extended the current conditional marketing…
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Enzo Biochem testifies Cervical Cancer Biomarker detection test

Jan 23, 2018
In order to offer a robust, and economically viable solution for anatomical pathology, Enzo Biochem asserted the authentication of a cervical Cancer biomarker detection test offering a…
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FDA approves Ready-to-Use Cardiovascular Medication Bivalirudin for Baxter

Jan 23, 2018
Baxter asserted the approval of U.S. Food and Drug Administration for Bivalirudin in 0.9 percent Sodium Chloride Injection (bivalirudin). Baxter's premixed medications are manufactured…
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FDA offers supplementary clearances to Bio-Rad’s IH-System Gel Reagents, Blood Typing Products

Jan 23, 2018
U.S FDA has granted 510 (k) clearance to Bio-Rad Laboratories for the IH-Incubator L and IH-Centrifuge L instruments to be used with the full range of Bio-Rad’s IH-System Gel Reagents…
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FDA extends Orphan Drug Designation to Enzychem Lifesciences’s EC-18 for treatment of ARS

Jan 23, 2018
Enzychem Lifesciences Corp asserted that the US Food and Drug Administration has granted Orphan Drug Designation to EC-18 for treating Acute Radiation Syndrome. US FDA Orphan Drug…
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Press Releases

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