Method of treating pain using nalbuphine and opioid antagonists
AssigneeThe Regents of the University of California
InventorJon D. Levine
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AssigneeThe Regents of the University of California
InventorJon D. Levine
Estimating the term…
Inflammatory or neuropathic pain in both men and women patients is treated by administering, sequentially or simultaneously, (a) nalbuphine and (b) an opioid antagonist selected from naloxone, naltrexone and nalmefene, or a salt or prodrug of nalbuphine and/or the opioid antagonist. Preferably, administration is made of (a) an amount of from about 3 to about 8 mg nalbuphine and (b) from about 0.2 to about 0.8 mg of an opioid antagonist selected from naloxone, naltrexone and nalmefene, or a salt and/or prodrug of either (in an amount that produces in a patient the same blood concentration of the compound in question as would administration of said amount of the nalbuphine or opioid antagonist itself). Treatment of both inflammatory and neuropathic pain can be achieved; side effects common with μ-opioids such as morphine were not observed.
A method of treating pain comprising administering to a human patient in need of such treatment
A method of treating neuropathic pain comprising administering to a human patient in need of such treatment (a) nalbuphine or a pharmaceutically acceptable salt of nalbuphine or a prodrug of nalbuphine, and (b) an opioid antagonist selected from the group consisting of naloxone, naltrexone, nalmefene, pharmaceutically acceptable salts thereof, and prodrugs therefor.
A pharmaceutical composition comprising an amount of nalbuphine or a pharmaceutically effective salt thereof or prodrug therefor, effective to treat neuropathic pain in a human patient, and a pain-relieving enhancing amount of an opioid antagonist selected from the group consisting of naloxone, naltrexone and nalmefene, pharmaceutically acceptable salts thereof and prodrugs therefor.
A pharmaceutical composition comprising (a) from about 3 to about 8 mg of nalbuphine or a pharmaceutically acceptable salt or prodrug of nalbuphine, said nalbuphine salt or prodrug being present in an amount that produces in the human patient the same blood concentration of nalbuphine as would administration of from 3 to 8 mg of nalbuphine;
Dependencies are inferred from the claim text.