http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2550035-T3

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-0056
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4178
filingDate 2007-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f268cb6f3982ed7fbb3a33db18503fd8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b6e485ac609cf337bc87d08c47bd76e
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publicationDate 2015-11-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2550035-T3
titleOfInvention Drug delivery systems comprising a weakly basic serotonin 5-HT3 selective blocking agent and organic acids
abstract A multiparticulate pharmaceutical dosage form comprising one or more populations of controlled pulsatile release (LPC) beads of a weakly basic drug; wherein the weakly basic drug comprises a selective serotonin blocking agent 5-HT3 containing nitrogen (N), or a pharmaceutically acceptable salt thereof, having a pKa in the range of about 5 to 14 and a solubility of no greater than about 200 µg / ml at pH 6.8; wherein the LPC beads comprise organic acid core particles comprising at least one pharmaceutically acceptable organic acid, having a barrier coating with an LS (sustained release) polymeric membrane comprising a non-water soluble polymer alone or in combination with a water-soluble polymer or an enteric polymer, in which the weakly basic drug is layered and further coated with a time-delayed membrane, so that both the organic acid and the weakly basic drug have comparable drug release profiles; and wherein the weakly basic drug and organic acid are not in contact with each other in the dosage form.
priorityDate 2006-01-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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