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Acasti Pharma invited to present the CaPre study results at National Lipid Association Scientific…

May 19, 2017
Acasti Pharma announced that it has received an invitation to present the CaPre (omega-3 phospholipid) study results at the National Lipid Association Scientific Sessions in…
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XOMA Earns $10 Million Milestone Payment as Another of its Licensed Assets

May 19, 2017
XOMA Corporation announced it has earned a $10 million milestone payment as one Company asset licensed to one of its pharmaceutical partners advances into clinical development. XOMA…
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FDA approves Jubilant’s Amlodipine and Olmesartan Medoxomil Tablets

May 19, 2017
Jubilant Life Sciences Ltd, announced that Jubilant Pharma Limited, a material wholly owned subsidiary of the Company, has received Abbreviated New Drug Application (ANDA)  final …
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FDA expands approved use of Kalydeco to treat cystic fibrosis

May 18, 2017
The U.S. FDA has expanded approved use of Vertex Pharmaceuticals manufactured Kalydeco (ivacaftor) for treating cystic fibrosis. The approval triples the number of rare gene mutations…
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FDA grants Octapharma orphan drug designation for Octagam 10%

May 18, 2017
The U.S. FDA has granted Octapharma with orphan drug designation for Octagam 10%. Octagam 10% is an immune globulin intravenous (human) liquid for the treatment of…
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Lilly selects Cogstate as preferred provider for Alzheimer Disease Platform

May 18, 2017
Cogstate Ltd announced that Eli Lilly’s has selected Cogstate as preferred provider for Alzheimer’s Disease Platform, to support with solutions to ensure high-quality neuropsychological…
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Concert Pharmaceuticals Announces Clinical Hold on CTP-543

May 18, 2017
Concert Pharmaceuticals received notice from the U.S. FDA that its CTP-543 Phase 2a clinical trial for alopecia areata has been placed on clinical hold. The FDA had previously…
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CytoDyn’s PRO 140 treats patient suffering from GvHD in Phase 2 trial

May 18, 2017
CytoDyn In. announced the treatment of the first patient suffering from GvHD(Graft versus Host Disease) with use of PRO 140 during its clinical trial Phase 2. The multicenter,…
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FDA approves Launch of Doxorubicin Hydrochloride Liposome Injection in the U.S. Market

May 18, 2017
Dr. Reddy’s Laboratories Ltd. announced that USFDA has approved to launch Doxorubicin Hydrochloride Liposome Injection for intravenous use, in the US market. The approval is an outcome…
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Dr. Donna Morgan Murray appointed as Nativis Chief Regulatory Officer

May 18, 2017
Dr. Donna Morgan Murray has been appointed as Nativis Chief Regulatory Officer with immediate effective. Murray is author of more than 60 publications in peer-referenced…
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