http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2343148-C

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filingDate 1999-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2005-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bf42f688a53f71139b655bfd8eeb64f5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6ecf288f52bcab88662e35542b718667
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8bd05f7db83d920901b171f953c5df71
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0bde3c4eb7369de08337c1fad8aca5af
publicationDate 2005-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2343148-C
titleOfInvention Quick release pharmaceutical compositions of drug substances
abstract The present invention relates to an oral modified release pharmaceutical composition for the administration of a therapeutically and/or prophylactically effective amount of an active substance (a drug substance) to obtain a relatively fast or quick onset of the therapeutic and/or prophylactic effect. The drug substances contained in a modified release pharmaceutical composition according to the invention are suitably a drug substance which has a very low solubility under acidic conditions, i.e. under conditions similar to those present in the stomach and/or drug substances which have a pK a value below about 5.5 such as in a range of from about 4 to about 5. The composition is based on a powder comprising a therapeutically and/or prophylactically active substance and has such a particle size that: when the powder is subjected to a sieve analysis, then at least about 90 % w/w of the particles passes through sieves 180 µm and the powder is contacted with an aqueous medium to form a particulate composition, which has such a particle size that when the particulate composition is subjected to a sieve analysis, then at least about 50 % w/w of the particles passes through sieve 180 µm. Furthermore, the composition, when tested in accordance with the dissolution method (I) defined herein employing 0.07 N hydrochloric acid as dissolution medium, releases at least about 50 % w/w of the active substance within the first 20 min of the test.
priorityDate 1998-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 600.