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    Home > Medical News > Medical Research Articles > Humanwell medicine class 3.1 antiemetic, fosapritam, dimethylmeglumine, has been accepted for clinical application

    Humanwell medicine class 3.1 antiemetic, fosapritam, dimethylmeglumine, has been accepted for clinical application

    • Last Update: 2020-04-03
    • Source: Internet
    • Author: User
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    According to the website of the State Food and Drug Administration (CFDA) on June 4, Yichang humanwell, a subsidiary of humanwell pharmaceutical Holding Co., Ltd., applied for the clinical application of fosapitam, a class 3.1 chemical drug, and fosapitam, a raw material drug and a preparation for injection, were accepted At present, there is no domestic enterprise to produce the product, and the original research drug has not entered the market of our country Fosapitam for injection is mainly used for the prevention and treatment of acute and delayed nausea and vomiting caused by chemotherapy It was first developed by Merck company and was listed in the United States in January 2008 It has entered Sweden, Czech Republic, Portugal, the United Kingdom and other countries, but has not yet entered China According to the public data, the purchase amount of antiemetics in sample hospitals has been increasing year by year In 2011, the drug purchase amount of sample hospitals exceeded 800 million yuan, and the total market size of the whole country is estimated to be 1.5-2 billion yuan Experts predict that palonosetron, aripitan and fosapitam are the three major antiemetics in the future CFDA shows that, at present, the original research drug of fosapitam for injection has not yet applied for registration in China Apart from Yichang humanwell, only Shandong Luoxin Pharmaceutical Co., Ltd has applied for the product  
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