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Business Wire 02/20/2019 16:10
FDA approval of pembrolizumab in the adjuvant setting is based on results from the KEYNOTE-054 trial.
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Activist Post 02/20/2019 14:56
Attorney Alan Phillips provided the following charts, which ought to cause “shock and awe” among parents, health departments everywhere, and even at HHS-CDC-FDA if they are open to factual science, not consensus fraudulent science.
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Upadacitinib, an investigational once-daily oral JAK1-selective inhibitor, is being studied for the treatment of adult patients with moderate to severe rheumatoid arthritis[1-8]. The New Drug Application (NDA) is supported by data from the global upadaci...
More from Healthcare Sales & Marketing Network: 02/19/2019 10:07
NORTH CHICAGO, Ill., Feb. 19, 2019/PRNewswire/ -- AbbVie (NYSE: ABBV), a research-based global biopharmaceutical company, has announced that the U.S. Food and Drug Administration (FDA) has accepted for priority review its New Drug Application (NDA) for upadacitinib for the treatment of adult patients with moderate to severe rheumatoid arthritis.
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PR Newswire 02/12/2019 10:12
That means accountability throughout the supply chain, including important oversight by the FDA to ensure every entity within the chain is complying with the law.
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Healio News 02/12/2019 09:43
Among the top stories in infectious disease last week were the FDA’s acceptance of a new drug application for two Merck antibacterial agents meant to treat complicated UTIs and intra-abdominal infections and President Donald J. Trump’s announcement of a goal of ending the HIV epidemic in the US by 2030 ...
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GlobeNewswire 02/12/2019 01:07
Media Release Copenhagen, Denmark, February 12, 2019.
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