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Agenda released for SMi Group’s Adaptive Designs in Clinical Trials 2018

Nov 23, 2017
Now running for 10 years, SMi Group’s annual conference on Adaptive Designs in Clinical Trials returns to London in Spring 2018, gathering a senior audience of experts to discuss and…
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Superbugs: Exclusive Interviews Released with ABAC Therapeutics, Alchemy Biomedical and Oppilotech

Nov 22, 2017
SMI REPORTS: Expert insight into tackling the scientific, regulatory and economic challenges to combat antimicrobial resistance. It is imperative for medical experts and drug…
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Zubsolv receives authorization for Treatment of Opioid Dependence in Europe

Nov 21, 2017
Orexo AB (publ.) announce that the European Medicines Agency (EMA) has granted a Marketing Authorization (MA) for Zubsolv (buprenorphine and naloxone), a novel rapidly-disintegrating…
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Novartis, ASCP and ACS join forces to fight cancer in Ethiopia, Uganda and Tanzania

Nov 21, 2017
Novartis, the American Society for Clinical Pathology (ASCP) and the American Cancer Society (ACS) announced that they will work together to devise a common approach to improve access…
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Ionis Pharmaceuticals Licenses Second Orally Delivered Antisense Drug to Janssen

Nov 21, 2017
Ionis Pharmaceuticals announced that it has licensed a second orally delivered Generation 2.5 antisense drug to Janssen Biotech, Inc. (Janssen) for which Ionis earned $5 million.…
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Cerecor acquires TRx Pharmaceuticals

Nov 21, 2017
Cerecor Inc. and TRx Pharmaceuticals, LLC (TRx) announced that the companies have entered into a purchase agreement in which Cerecor will acquire TRx, including subsidiary Zylera…
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Samsung Bioepis receives regulatory approval for Trastuzumab Biosimilar, ONTRUZANT

Nov 21, 2017
Samsung Bioepis Co., Ltd. announced the European Commission’s (EC) marketing authorization of ONTRUZANT, a biosimilar referencing Herceptin (trastuzumab), for the treatment of early…
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AVEO Oncology appoints Nikil Mehta as SVP of Regulatory and Quality Assurance

Nov 21, 2017
AVEO Oncology announced the appointment of Nikhil Mehta, Ph.D., as Senior Vice President of Regulatory and Quality Assurance, effective November 20, 2017. In this role, Dr. Mehta will…
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Revance announces Orphan Drug Designation of RT002 for the Treatment of Cervical Dystonia

Nov 21, 2017
Revance Therapeutics announced that the U.S. Food and Drug Administration (FDA) granted orphan drug designation for the Company’s product candidate, DaxibotulinumtoxinA for Injection…
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Faslodex receives FDA approval for the treatment of advanced breast cancer in combination with…

Nov 21, 2017
AstraZeneca announced that the US Food and Drug Administration (FDA) has approved a new indication for Faslodex(fulvestrant), expanding the indication to include use with abemaciclib, a…
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