http://rdf.ncbi.nlm.nih.gov/pubchem/patent/PL-198034-B1

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filingDate 2000-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e9b474deaa17246034975a70e90790c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_57d2a5af0baf45e7f4768143d3429245
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8ef174334524cadcc2010a1c99faa677
publicationDate 2008-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PL-198034-B1
titleOfInvention A non-interacting pharmaceutical combination, including the HMG-CoA reductase inhibitor, which is (E) -7- [4- (4-fluorophenyl) -6-isopropyl-2- [methyl (methylsulfonyl) amino] pyrimidin-5-yl] acid (3R, 5S) -3,5-dihydroxyhept-6-ene or a pharmaceutically acceptable salt thereof and its use
abstract The invention concerns safe non-interacting drug combinations of a 3-hydroxy -3- methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor, which is (E)-7- [4-(4-fluorophenyl) -6- isopropyl -2- [methyl (methylsulfonyl) amino] pyrimidin-5-yl] (3R,5S)-3,5- dihydroxyhept -6-enoic acid or a pharmaceutically acceptable salt thereof (the Agent) and a drug which is either an inducer, inhibitor or a substrate of cytochrome P450, in particular cytochrome P450 isoenzyme 3A4. Particular combinations are useful in treating hyperlipidaemia in humans who are receiving immunosuppressive chemotherapy. A preferred combination is the Agent and a fibrate drug, the use of such a combination in treating hyperlipidaemia in mammals, and medicaments containing such a combination for use in such treatments.
priorityDate 1999-02-06-04:00^^<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: 764.