http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2527856-A1

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filingDate 2004-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_71ea97029e5292e3a31678648b0964bd
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7220e6be8c29c020fed0711921c25c91
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_54740c1625bbda33ec1c1f046e9d8fc3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b6c3d4be824ba736e5607ec32f4f12e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_26ed63498df2f132abcd2844e74e774d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_df89ad17efbbbb2caf93ae1dd5fca42a
publicationDate 2004-12-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2527856-A1
titleOfInvention Substituted 1, 4-di-piperidin-4-yl-piperazine derivative combined with an opioid analgesic and their use for the treatment of pain and side-effects associated with opioid-based treatments
abstract This invention concerns novel formulations for opioid-based treatments of pain and/or nociception comprising opioid analgesics and 1,4-di-piperidin-4-yl-piperazine derivatives having neurokinin antagonistic activity, in particular NK1 antagonistic activity, the use of said formulation for the manufacture of a medicament for the prevention and/or treatment of emesis, pain and/or nociception, in particular in opioidbased acute and chronic pain treatments, more in particular in inflammatory, postoperative, emergency room (ER), breakthrough, neuropathic and cancer pain treatments and the use of an NK1-receptor antagonist for the manufacture of a medicament for the prevention and/or treatment of respiratory depression in opioid-based treatments of pain. The pharmaceutical formulations according to the invention comprise a pharmaceutically acceptable carrier and, as active ingredients, a therapeutically effective amount of an opioid analgesic and NKI -antagonists according to the general Formula (I) the pharmaceutically acceptable acid or base addition salts thereof, the stereochernically isomeric forms thereof, the N-oxide form thereof and prodrugs thereof, wherein all substituents are defined as in Claim 1. The pharmaceutical composition according to the invention reduces to a large extent a number of unwanted side~effects associated with opioid analgesics, in particular emesis, respiratory depression and tolerance, thereby increasing the total tolerability of said opioids in pain treatment.
priorityDate 2003-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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