http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-200404580-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-0004
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filingDate 2003-07-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ef4e07f89e7a2d67b02fc964bb8f9e63
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b40292ebb77123400500fce86f85e20e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ba3562fbc394c5ffad551cd872c4e016
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b37356171bff72e1dbdb2eba060c6034
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publicationDate 2004-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-200404580-A
titleOfInvention Controlled-release pharmaceutical formulations
abstract The invention provides controlled release pharmaceutical formulations having a coated core with the core comprising a drug-containing composition and a water-swellable composition, each occupying essentially separate regions within the core. The drug-containing composition comprises a PDE4D inhibitor, or a pharmaceutically acceptable salt thereof, preferably (R)-2-[4-({[2- (benzo[1, 3]dioxol-5-yloxy)-pyridine-3-carbonyl]-amino}-methyl)-3-fluoro-phenoxy]-propionic acid, or a pharmaceutically acceptable salt thereof, or 2-(4-fluorophenoxy)-N-[4-(1-hydroxy-1-methyl-ethyl)-benzylJ-nicotinamide, or a pharmaceutically acceptable salt thereof, and a drug-entraining agent. The coating around the core is water-permeable, water-insoluble, and has at least one delivery port therethrough. The invention further provides methods of reducing the nausea and emetic effects of PDE4D inhibitors, and controlled-release formulations having improved PDE4D inhibitor in vivo and in vitro profiles.
priorityDate 2002-07-03-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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