http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-3065718-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_32bfa35cf6237278dc0e6c46927fbe2e
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-20
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K9-2031
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-64
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-26
filingDate 2013-12-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c0dedf27aa02fdc3b76bed56f47f5cf8
publicationDate 2016-09-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-3065718-A1
titleOfInvention Controlled-release formulations comprising torsemide
abstract Disclosed herein are controlled-release (GR, e.g., extended-release (ER) or prolonged- release (PR)) oral dosage formulation comprising an effective amount of Torsemide or a pharmaceutically acceptable salt thereof and at least one sustained release excipient comprising a polymer, wherein the at least one matrix component is selected from the group consisting of: hydroxy propyl cellulose (HPC), hydroxpropyl methyl cellulose (HPMC), glyceryl behenate, and a polyethylene glycol glyceride. Torsemide may be present in the formulation in a range of about 1 wt% to about 20 wt%, or about 5 wt% to about 10 wt% and the matrix component is present in the formulation in a range of about 5 wt% to about 50 wt%, or about 15 wt% to about 35 wt%. The formulation may further comprise at least one binder, lactose, talc and magnesium stearate. Methods of making and using the controlled-release oral dosage Torsemide formulation are also disclosed. A novel mechanism for Torsemide action in diuresis is further disclosed.
priorityDate 2013-10-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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