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filingDate 2014-03-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_cb292e7c413a56392f964482ab0978d4
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publicationDate 2019-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EA-032322-B1
titleOfInvention SOLID ORAL DOSED COMPOSITION OF HCV INHIBITOR IN AMORPHOUS CONDITION
abstract This application describes solid oral dosage forms containing compound (1) or its pharmaceutically acceptable salt, where compound (1) is in an amorphous state. Also described are solid oral dosage forms comprising the composition of the compound (1) in an amorphous state and one or more pharmaceutically acceptable excipients. Compound (1) is a specific inhibitor of the hepatitis C virus (HCV) NS3 / 4A serine protease. This application also describes methods for using solid oral dosage forms to treat HCV infection. Processes for the production of solid oral dosage forms are also described.
priorityDate 2013-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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