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Glenmark Pharmaceuticals and Harbour BioMed Sign Agreement for Greater China to Develop GBR 1302

Aug 7, 2018
Glenmark Pharmaceuticals S.A. and Harbour BioMed announced that they have entered into an exclusive license agreement for the Greater China territory to develop, manufacture and…
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Abzena Signs Protein Engineering Agreement with NYU Langone Health

Aug 6, 2018
Abzena plc has entered into a master service agreement with one of America’s leading academic medical centres, NYU Langone Health (New York, US). The agreement, for protein engineering…
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Selumetinib granted orphan designation in Europe for neurofibromatosis type 1

Aug 6, 2018
AstraZeneca and Merck & Co., Inc., Kenilworth, NJ, US (known as MSD outside the US and Canada) announced that the European Medicines Agency (EMA) has granted orphan designation to…
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Amgen Breaks Ground On Next-Generation Biomanufacturing Plant In Rhode Island

Aug 3, 2018
Amgen announced the groundbreaking of its new next-generation biomanufacturing plant that will be constructed at its West Greenwich, R.I. campus. The new plant is the first-of-its-kind…
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Akcea and PTC Collaborate to Commercialize Two Rare Disease Drugs in Latin America

Aug 3, 2018
PTC Therapeutics and Akcea Therapeutic an affiliate of Ionis Pharmaceuticals announced a collaboration under which PTC will commercialize two of Akcea's rare disease drugs in Latin…
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PRIME designation granted by EMA for RG6042 for treatment of Huntington’s disease

Aug 3, 2018
Roche announced that the European Medicines Agency (EMA) has granted PRIME (PRIority MEdicines) designation for the company’s investigational medicine RG6042 (formerly known as…
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Novartis marks a new era for migraine patients with the EU approval of Aimovig

Aug 3, 2018
Novartis announced that the European Commission (EC) approved Aimovig (erenumab) for the prevention of migraine in adults experiencing four or more migraine days per month. Aimovig is…
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Selumetinib granted orphan designation in Europe for neurofibromatosis type 1

Aug 3, 2018
AstraZeneca and Merck & Co., Inc., Kenilworth, NJ, US (known as MSD outside the US and Canada) announced that the European Medicines Agency (EMA) has granted orphan designation to…
Read More...

Takeda to Produce Innovative Drug for Multiple Myeloma Patients in Yaroslavl, Russia

Aug 3, 2018
Takeda Pharmaceutical Company Limited announced the opening of a production site for NINLARO (ixazomib), an innovative drug for patients with multiple myeloma, at its Yaroslavl plant.…
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Pfizer Receives European Approval for Oncology Biosimilar, TRAZIMERA (trastuzumab)

Aug 3, 2018
Pfizer Inc. announced the European Commission (EC) has approved TRAZIMERA, a biosimilar to Herceptin (trastuzumab), for the treatment of human epidermal growth factor (HER2)…
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