U.S. patents available from 1976 to present.
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Method of treating pain by administering 24 hour oral opioid formulations

Patent 5672360 Issued on September 30, 1997. Estimated Expiration Date: Icon_subject July 22, 2016. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

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Preparation of aqueous alcoholic dispersions of pH sensitive polymers and plasticizing agents and a method of enteric coating dosage forms using same
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Inventors

Assignee

Application

No. 578688 filed on 07/22/1996

US Classes:

424/490, Coated (e.g., microcapsules)424/468, Sustained or differential release type424/480, Cellulose or derivative424/494, Cellulose derivatives424/497Containing solid synthetic polymers

Examiners

Primary: Page, Thurman K.
Assistant: Benston, William E. Jr.

Attorney, Agent or Firm

Foreign Patent References

  • 9047732 AU. 07/13/1990
  • 9341654 AU. 02/13/1995
  • 0097523 EP 01/13/1984
  • 0108218 EP 05/13/1984
  • 0147780 EP 07/13/1985
  • 0235986 EP 09/13/1987
  • 0253104 EP 01/13/1988
  • 0271193 EP 06/13/1988
  • 377518A2 EP. 07/13/1990
  • 0388954 EP 09/13/1990
  • 0415693 EP 03/13/1991
  • 0532348 EP 03/13/1993
  • 0534628 EP 03/13/1993
  • 0535841 EP 04/13/1993
  • 0548448 EP 06/13/1993
  • 0546676 EP 06/13/1993
  • 0580860 EP 02/13/1994
  • 0636370 EP 06/13/1994
  • 0665010 EP 08/13/1995
  • 377518B1 EP. 02/13/1996
  • 2178313 GB 02/13/1987
  • WO9201446 WO 02/13/1992
  • WO9206679 WO 04/13/1992
  • WO9304675 WO 03/13/1993
  • WO9310765 WO 06/13/1993
  • WO9318753 WO 09/13/1993
  • WO9403161 WO 02/13/1994
  • WO9422431 WO 10/13/1994
  • WO9600066 WO 01/13/1996
  • WO9601629 WO 01/13/1996
  • WO9614058 WO 03/13/1996

International Classes

A61K 009/16
A61K 009/50

Abstract

Patients are treated with 24-hour oral sustained release opioid formulations which, upon administration, provide an initially rapid opioid absorption such that the minimum effective analgesic concentration of the opioid is more quickly achieved. These sustained release opioid formulations include an effective amount of at least one retardant material to cause said opioid analgesic to be released at a such a rate as to provide an analgesic effect after oral administration to a human patient for at least about 24 hours, and are characterized by providing an absorption half-life from 1 to about 8 hours. A method of titrating a human patient utilizing these sustained release opioid formulations is also disclosed.

Other References

  • A protocol for a clinical study entitled "A Randomized, Double-Blind, Parallel-Group Study comparing the Efficacy and Safety of Kapanol.RTM. to Ms Contin.RTM. in the Management of Patients with Moderate to Severe Cancer Pain" (the Protocol). The date of the Protocol is indicated as Feb. 10, 1992 and it bears CDD No. 14556. The sponsor of the study is indicated to be Faulding Pharmaceuticals, an Australian company
  • Certain Patient Diary Cards, Drug Disposition Records, Case Report Forms and a listing which apparently correlates patient randomization number with the treatment or dosing regiment assigned to each patient
  • Patient consent forms, apparently for four study participants
  • Certain documents regarding Institutional Review Board Approval for the Faulding-sponsored study
  • Investigator Agreements between the study organizers and certain of the principal investigators
  • Advertisement:Roxanol SR, .COPYRGT.1988 Roxane Laboratories, Inc
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