http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2946154-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9e5e4772677c4b7cd687a496a7b07001
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P29-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-209
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-407
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-407
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P29-00
filingDate 2014-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_29637517e3312202e5b44ae6ac36cda2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_359ac7e775f001477f62f8b4bf099efb
publicationDate 2015-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2946154-A1
titleOfInvention Three-phase system for modified release of a non-steroidal antiinflammatory
abstract The present invention relates to a novel pharmaceutical composition in solid form comprising a non-steroidal antiinflammatory and/or the pharmaceutically acceptable salts thereof, which consists of a tablet comprising a three-phase system for modified release, which phases are: a) a delayed-release core characterized in that it is located at the centre of the composition; b) a lower, immediate-release layer, characterized in that it totally and/or partially covers the core; and c) an upper, extended-release layer, characterized in that it totally and/or partially covers the core. Said composition is administered orally and used in the treatment of slight to moderate pain caused by cephalalgia, myalgia, arthralgia, ocular pain, photophobia, a burning sensation secondary to ocular surgery, post-operative pain, neuropathic pain, inflammation, inter alia.
priorityDate 2013-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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