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Thermo Fisher Scientific Opens U.S. Precision Medicine Science Center

Jun 11, 2018
Thermo Fisher Scientific Inc. officially opened its U.S. Precision Medicine Science Center (PMSC) in Cambridge, Mass. The Center offers access to advanced "omics" technologies and…
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FDA Approves Genentech’s Rituxan (rituximab) For Pemphigus Vulgaris

Jun 8, 2018
Genentech announced that the U.S. Food and Drug Administration (FDA) has approved Rituxan (rituximab) for the treatment of adults with moderate to severe pemphigus vulgaris (PV), a…
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GE Healthcare FlexFactory Helps XPH Scale Up Industrialization of TCR T-Cell Immunotherapy Drugs

Jun 8, 2018
GE Healthcare will provide Xiangxue Pharmaceutical Co., Ltd. (XPH) with a FlexFactory for cell therapy, a semi-automated end-to-end manufacturing platform, to help scale up, digitize…
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Vetter Strikes out on New Pathways to Further Develop the Injection Process

Jun 8, 2018
How can digital trends be used purposefully in regards to the application of injection systems? That is the key question being addressed by Vetter’s Open Innovation Challenge. This new…
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Blueprint Medicines and CStone Pharmaceuticals Announce Exclusive Collaboration and License…

Jun 8, 2018
Blueprint Medicines Corporation and CStone Pharmaceuticals announced an exclusive collaboration and license agreement for the development and commercialization of avapritinib, BLU-554…
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Celltrion Launches Bio CDMO Business for the Development of New Drugs

Jun 8, 2018
Celltrion made an announcement that it will launch Bio CDMO (Contract Development and Manufacturing) business, in a bid to pursue open innovation for development of new drugs, at the…
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Biogen Enters Exclusive Option Agreement to Acquire TMS’ Phase 2 Asset for Acute Stroke

Jun 8, 2018
Biogen announced that it has entered into an exclusive option agreement with TMS Co., Ltd. to acquire TMS-007 and backup compounds. The agreement includes an upfront payment of $4…
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FDA and EMA Accept Regulatory Submissions for Review of Talazoparib

Jun 8, 2018
Pfizer Inc. announced that the U.S. Food and Drug Administration accepted for filing and granted Priority Review designation to the company’s New Drug Application for talazoparib. The…
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Chimerix Receives Orphan Drug Designation from the FDA for Brincidofovir for the Treatment of…

Jun 8, 2018
Chimerix announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation for brincidofovir for the treatment of smallpox. Chimerix has been working…
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Ironwood Pharmaceuticals Announces FDA Orphan Drug Designation for Olinciguat for the Treatment of…

Jun 8, 2018
Ironwood Pharmaceuticals announced that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation to olinciguat (IW-1701) for the treatment of patients with sickle…
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Pharma Journalist is a product of Kellen Media. Pharma Journalist is one of the leading website covering the need of global Pharmaceutical Industry.

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