Analgesic compositions containing buprenorphine

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C514S811000, C514S812000

Reexamination Certificate

active

06995169

ABSTRACT:
An analgesic composition in parenteral unit dosage form or in a unit dosage form suitable for delivery via the mucosa comprising an amount of buprenorphine which is less than the clinical dose required to achieve pain relief and an amount of naloxone such that the ratio by weight of buprenorphine to naloxone is in the range of from 12.5:1 to 27.5:1, or an amount of naltrexone or nalmefene such that the ratio by weight of buprenorphine to naltrexone or nalmefene is in the range of from 12.5:1 to 22.5:1. The analgesic action of the buprenorphine is potentiated by the low dose of naloxone, naltrexone or nalmefene.

REFERENCES:
patent: 5512578 (1996-04-01), Crain et al.
patent: 2 150 832 (1985-07-01), None
patent: 2 167 832 (1986-06-01), None
patent: 2167663 (1986-06-01), None
patent: WO 96/02251 (1996-02-01), None
XP-001010201, Thomas Eissenberg et al., “Buprenorphine's Physical Dependence Potential: Antagonist-Precepitated Withdrawal in Humans 1”, The Journal of Pharmacology and Experimental Therapeutics, The American Society for Pharmacology and Experimental Therapeutics, JPET vol. 276: pp. 449-459, 1996.

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