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HCATS and Ori Biotech Announce a Joint Development Agreement

Jan 22, 2020
Hitachi Chemical Advanced Therapeutics Solutions, LLC (HCATS), a US subsidiary of Hitachi Chemical Co., Ltd. that engages in contract manufacturing and manufacturing development of cell…
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Horizon Therapeutics gets FDA approval for thyroid eye disease drug

Jan 22, 2020
Horizon Therapeutics plc announced that the U.S. Food and Drug Administration (FDA) has approved TEPEZZATM (teprotumumab-trbw) for the treatment of Thyroid Eye Disease (TED). TEPEZZA is…
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GSK: FDA grants priority review of belantamab mafodotin for patients with relapsed or refractory…

Jan 22, 2020
GlaxoSmithKline plc announced the US Food and Drug Administration (FDA) granted a priority review for the company’s Biologics License Application (BLA) seeking approval of belantamab…
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FDA approves first treatment for thyroid eye disease

Jan 21, 2020
Today, the U.S. Food and Drug Administration (FDA) approved Tepezza (teprotumumab-trbw) for the treatment of adults with thyroid eye disease, a rare condition where the muscles and…
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Armas Pharmaceuticals Adds Four Generic Injectables As First Launches of 2020

Jan 21, 2020
Armas Pharmaceuticals Inc. (Armas), has begun the new year with launches of four generic injectables: Caffeine Citrate, Docetaxel, Gemcitabine and Verapamil HCI. These products are now…
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SMi’s Pharmaceutical Microbiology in Boston – what to expect over the 2 day conference

Jan 21, 2020
SMi Reports: SMi’s Pharmaceutical Microbiology Conference series will feature an exciting agenda and expert speaker line-up. SMi Group are pleased to host the 3rd Annual…
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Imfinzi and tremelimumab granted Orphan Drug Designation in the US for liver cancer

Jan 21, 2020
AstraZeneca’s Imfinzi (durvalumab) and tremelimumab, an anti-CTLA4 antibody and potential new medicine, have both been granted Orphan Drug Designation (ODD) in the US for the treatment…
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Novartis announces EU approval of Mayzent (siponimod) for adult patients with SPMS with active…

Jan 21, 2020
Novartis announced the European Commission (EC) has approved Mayzent (siponimod) for the treatment of adult patients with secondary progressive multiple sclerosis (SPMS) with active…
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FDF China to be held in June to boost Chinese pharmaceutical enterprises to “go global”…

Jan 21, 2020
FDF China, collocated with CPhI China, will be held from June 22-24, 2020 at Shanghai New International Expo Centre (SNIEC). More and more formulation enterprises need to implement…
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Discover the Latest Information and Seize Market Opportunities in the Annual Event of the CRO &…

Jan 21, 2020
As the pharmaceutical market demands in China continue to grow, China’s pharmaceutical policies become gradually clear, which provides broad space for the development of pharmaceutical…
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