http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2747845-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_506e5cddcc1b2fd25e66858a3bdb8622
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-12
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-522
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-52
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K9-10
filingDate 2006-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_69445ee42ba6298e2c622060dab33e6b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7fc80d99517d77166a17116d2a79f248
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dfa5037c547902cef61b1fd8de9b9574
publicationDate 2007-06-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2747845-A1
titleOfInvention Compositions and methods for dermally treating pain
abstract The present invention is drawn to solidifying formulations for dermal delivery of a drug for treating pain, such as musculoskeletal pain, inflammation, joint pain, or neuropathic pain. The formulation can include a drug selected from certain drug classes, a solvent vehicle, and a solidifying agent. The solvent vehicle can include a volatile solvent system comprising at least one volatile solvent, and a non-volatile solvent system comprising at least one non-volatile solvent, wherein the evaporation of at least some of the volatile solvent converts the formulation on the skin into a solidified layer and the non-volatile solvent system is capable of facilitating the topical delivery of the drug(s) at therapeutically effective rates over a sustained period of time.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111067919-A
priorityDate 2005-12-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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