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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-706
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-7068
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-02
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filingDate 2012-04-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2020-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_169835a6d4553c773423eb45c4830f61
publicationDate 2020-02-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2743691-T3
titleOfInvention Dosage regimen for sapacitabine and decitabine in combination to treat acute myeloid leukemia
abstract i) Sapacitabine, or a metabolite thereof which is CNDAC; and (ii) decitabine; for use in the treatment of AML, wherein sapacitabine, or a metabolite thereof, and decitabine are administered according to a dosage regimen comprising at least one first cycle of treatment and at least one second cycle of treatment, in wherein said first course of treatment comprises administering a therapeutically effective amount of decitabine for 5 consecutive days followed by a rest period of from 3 to 5 weeks, or until treatment-related toxicities are resolved, whichever is longer; and wherein said second cycle of treatment comprises administering a therapeutically effective amount of sapacitabine, or metabolite thereof, at a dose of 100 to 400 mg b.i.d., for 3 consecutive days per week, for 2 weeks followed by a rest period 2 to 4 weeks, or until treatment-related toxicities resolve, whichever is longer.
priorityDate 2011-04-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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