CA2339192A1 - Treatment of addiction and addiction-related behavior - Google Patents
Treatment of addiction and addiction-related behavior Download PDFInfo
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- CA2339192A1 CA2339192A1 CA002339192A CA2339192A CA2339192A1 CA 2339192 A1 CA2339192 A1 CA 2339192A1 CA 002339192 A CA002339192 A CA 002339192A CA 2339192 A CA2339192 A CA 2339192A CA 2339192 A1 CA2339192 A1 CA 2339192A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/4535—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a heterocyclic ring having sulfur as a ring hetero atom, e.g. pizotifen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A61K31/137—Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine or methadone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/197—Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid, pantothenic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/221—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin with compounds having an amino group, e.g. acetylcholine, acetylcarnitine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/32—Alcohol-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/34—Tobacco-abuse
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/36—Opioid-abuse
Abstract
The present invention provides a method for changing addiction-related behavior of a mammal suffering from addiction to abused drugs. The method includes administering to the manimal an effective amount of gamma vinylGABA (GVG) or a pharmaceutically acceptable salt thereof, or an enantiomer or a racemic mixture thereof, wherein the effective amount is sufficient to diminish, ihhibit or eliminate behavior associated with craving or use of abused drugs.
Claims (79)
- WHAT IS CLAIMED IS:
Use of gamma vinylGABA (GVG) for preparing a medicament useful for changing addiction-related behavior of a primate suffering from addiction to drugs of abuse by administering said medicament to said primate in an amount sufficient to diminish, inhibit or eliminate behavior associated with craving of drugs of abuse. - 2. The use according to Claim 1, wherein said elimination of behavior associated with craving of drugs of abuse occurs in the absence of an aversive response or appetitive response to GVG.
- 3. The use according to Claim 1, wherein said drug of abuse is selected from the group consisting of cocaine, morphine and nicotine.
- 4. The use according to Claim 1, wherein said medicament contains GVG
in an amount of about 100mg/kg to about 300mg/kg. - 5. The use according to Claim 1, wherein said medicament contains GVG
in an amount from about 150mg/kg to about 300mg/kg. - 6. The use according to Claim 1, wherein said addiction related behavior is conditioned place preference.
- 7. Use of gamma vinylGABA (GVG) for preparing a medicament useful for changing addiction-related behavior of a primate suffering from addiction to drugs of abuse by administering said medicament to said primate in an amount sufficient to attenuate the rewarding/incentive effects of drugs of abuse selected from the group consisting of cocaine, morphine and nicotine in the absence of altering rewarding/incentive effects of food in said primate.
- 8. The use according to Claim 7, wherein the rewarding/incentive effects of drugs of abuse is attenuated in the absence of an alteration in the locomotor function of said primate.
- 9. Use of gamma vinylGABA (GVG) for preparing a medicament useful for ameliorating effects of nicotine addiction in a primate by administering said medicament to said primate in an amount sufficient to reduce nicotine dependency characteristics.
- 10. The use according to Claim 9, wherein said medicament contains GVG
in an amount from about 75mg/kg to about 150mg/kg. - 11. The use according to Claim 9, wherein said medicament contains GVG
in an amount from about 18mg/kg to about 20mg/kg. - 12. The use according to Claim 9, wherein said nicotine dependency characteristics are reduced in the absence of an aversive response or appetitive response to GVG.
- 13. The use according to Claim 9, wherein said nicotine dependency characteristics are reduced in the absence of an alteration in the locomotor function of said primate.
- 14. Use of gamma vinylGABA (GVG) for preparing a medicament useful for changing addiction-related behavior of a mammal suffering from addiction to drugs of abuse by administering said medicament to said mammal in an amount sufficient to diminish, inhibit or eliminate behavior associated with craving of drugs of abuse.
- 15. The use according to Claim 14, wherein said elimination of behavior associated with craving of drugs of abuse occurs in the absence of an aversive response or appetitive response to GVG.
- 16. The use according to Claim 14, wherein said drug of abuse is selected from the group consisting of psychostimuiants, narcotic analgesics, alcohols or nicotine and combinations thereof.
- 17. The use according to Claim 14, wherein said drug of abuse is selected from the group consisting of cocaine, nicotine, methamphetamine, ethanol, morphine, heroin and combinations thereof.
- 18. The use according to Claim 14, wherein GVG is administered in an amount of about 15mg/kg to about 600mg/kg.
- 19. The use according to Claim 14, wherein said addiction related behavior is conditioned place preference.
- 20. Use of gamma vinylGABA (GVG) or a pharmaceutically acceptable salt thereof, for preparing a medicament useful for changing addiction-related behavior of a mammal suffering from addiction to drugs of abuse by administering an effective amount of the medicament to the mammal, wherein the effective amount attenuates the rewarding/incentive effects of drugs of abuse selected from the group consisting of psychostimulants, narcotic analgesics, alcohols, nicotine and combinations thereof in the absence of altering rewarding/incentive effects of food in said mammal.
- 21. The use according to Claim 20, wherein the rewarding/incentive effects of drugs of abuse is attenuated in the absence of an alteration in the locomotor function of said mammal.
- 22. Use of gamma vinylGABA (GVG) or a pharmaceutically acceptable salt thereof for preparing a medicament useful for ameliorating effects of psychostimulant, narcotic analgesic, alcohol or nicotine addiction in a mammal by administering an effective amount of the medicament to the mammal, wherein the effective amount is sufficient to reduce psychostimulant, narcotic analgesic, alcohol or nicotine dependency characteristics.
- 23. The use according to Claim 22, wherein GVG is administered in an amount from about 15mg/kg to about 600mg/kg.
- 24. The use according to Claim 22, wherein said psychostimulant, narcotic analgesic, alcohol or nicotine dependency characteristics are reduced in the absence of an aversive response or appetitive response to GVG.
- 25. The use according to Claim 22, wherein said psychostimulant, narcotic analgesic, alcohol or nicotine dependency characteristics are reduced in the absence of an alteration in the locomotor function of said mammal.
- 26. Use of gamma vinylGABA (GVG) or a pharmaceutically acceptable salt thereof, or an enantiomer or a racemic mixture thereof, for preparing a medicament useful for changing addiction-related behavior of a mammal suffering from addiction to drugs of abuse by administering an effective amount of the medicament to the mammal, wherein the effective amount is sufficient to diminish, inhibit or eliminate behavior associated with craving or use of drugs of abuse.
- 27. The use according to Claim 26, wherein said elimination of behavior associated with craving of drugs of abuse occurs in the absence of an aversive response or appetitive response to GVG.
- 28. The use according to Claim 26, wherein said drug of abuse is selected from the group consisting of psychostimulants, narcotic analgesics, alcohols or nicotine and combinations thereof.
- 29. The use according to Claim 26, wherein said drug of abuse is selected from the group consisting of cocaine, nicotine, methamphetamine, ethanol, morphine, heroin and combinations thereof.
- 30. The use according to Claim 26, wherein GVG is administered in an amount of about 15mg/kg to about 600mg/kg.
- 31. The use according to Claim 26, wherein said addiction related behavior is conditioned place preference.
- 32. Use of gamma vinylGABA (GVG) or a pharmaceutically acceptable salt thereof, or an enantiomer or a racemic mixture thereof, for preparing a medicament useful for changing addiction-related behavior of a mammal suffering from addiction to drugs of abuse by administering an effective amount of the medicament to the mammal, wherein the effective amount attenuates the rewarding/incentive effects of drugs of abuse selected from the group consisting of psychostimulants, narcotic analgesics, alcohols, nicotine and combinations thereof in the absence of altering rewarding/incentive effects of food in said mammal.
- 33. The use according to Claim 32, wherein the rewarding/incentive effects of drugs of abuse is attenuated in the absence of an alteration in the locomotor function of said mammal.
- 34. Use of gamma vinylGABA (GVG) or a pharmaceutically acceptable salt thereof, or an enantiomer or a racemic mixture thereof for preparing a medicament useful for ameliorating effects of psychostimulant, narcotic analgesic, alcohol or nicotine addiction in a mammal by administering an effective amount of the medicament to the mammal, wherein the effective amount is sufficient to reduce psychostimulant, narcotic analgesic, alcohol or nicotine dependency characteristics.
- 35. The use according to Claim 34, wherein GVG is administered in an amount from about l5mg/kg to about 600mg/kg.
- 36. The use according to Claim 34, wherein said psychostimulant, narcotic analgesic, alcohol or nicotine dependency characteristics are reduced in the absence of an aversive response or appetitive response to GVG.
- 37. The use according to Claim 34, wherein said psychostimulant, narcotic analgesic, alcohol or nicotine dependency characteristics are reduced in the absence of an alteration in the locomotor function of said mammal.
- 38. Use of a composition that increases central nervous system GABA
levels for preparing a medicament useful for changing addiction-related behavior of a mammal suffering from addiction to drugs of abuse by administering an effective amount of the medicament to the mammal, wherein the effective amount is sufficient to diminish, inhibit or eliminate behavior associated with craving or use of drugs of abuse. - 39. The use according to Claim 38, wherein said medicament comprises GVG, gabapentin, valproic acid, progabide, gamma-hydroxybutyric acid, fengabine, cetylGABA, topiramate, tiagabine, acamprosate or a pharmaceutically acceptable salt thereof, or an enantiomer or a racemic mixture thereof.
- 40. The use according to Claim 38, wherein said elimination of behavior associated with craving of drugs of abuse occurs in the absence of an aversive response or appetitive response to the medicament.
- 41. The use according to Claim 38, wherein said drug of abuse is selected from the group consisting of psychostimulants, narcotic analgesics, alcohols or nicotine and combinations thereof.
- 42. The use according to Claim 38, wherein said drug of abuse is selected from the group consisting of cocaine, nicotine, methamphetamine, ethanol, morphine, heroin and combinations thereof.
- 43. The use according to Claim 38, wherein said addiction related behavior is conditioned place preference.
- 44. The use according to Claim 38, wherein said medicament comprises gabapentin administered in an amount of about 500mg to about 2g/day.
- 45. The use according to Claim 38, wherein said medicament comprises valproic acid administered in an amount of about 5mg/kg to about 100 mg/kg/day.
- 46. The use according to Claim 38, wherein said medicament comprises topiramate administered in an amount of about 50mg to about 1g/day.
- 47. The use according to Claim 38, wherein said medicament comprises progabide administered in an amount of about 250mg to about 2g/day.
- 48. The use according to Claim 38, wherein said medicament comprises fengabine administered in an amount of about 250mg to about 4g/day.
- 49. The use according to Claim 38, wherein said medicament comprises gamma-hydroxybutyric acid administered in an amount of about 5mg/kg to about 100 mg/kg/day.
- 50. Use of a composition that increases central nervous system GABA
levels for preparing a medicament useful for changing addiction-related behavior of a mammal suffering from addiction to drugs of abuse by administering an effective amount of the medicament to the mammal, wherein the effective amount attenuates the rewarding/incentive effects of drugs of abuse selected from the group consisting of psychostimulants, narcotic analgesics, alcohols, nicotine and combinations thereof in the absence of altering rewarding/incentive effects of food in said mammal. - 51. The use according to Claim 50, wherein said medicament comprises GVG, gabapentin, valproic acid, progabide, gamma-hydroxybutyric acid, fengabine, cetylGABA, topiramate, tiagabine, acamprosate or a pharmaceutically acceptable salt thereof, or an enantiomer or a racemic mixture thereof.
- 52. The use according to Claim 50, wherein the rewarding/incentive effects of drugs of abuse is attenuated in the absence of an alteration in the locomotor function of said mammal.
- 53. Use of a composition that increases central nervous system GABA
levels for preparing a medicament useful for ameliorating effects of psychostimulant, narcotic analgesic, alcohol or nicotine addiction in a mammal by administering an effective amount of the medicament to the mammal, wherein the effective amount is sufficient to reduce psychostimulant, narcotic analgesic, alcohol or nicotine dependency characteristics. - 54. The use according to Claim 53, wherein said medicament comprises GVG, gabapentin, valproic acid, progabide, gamma-hydroxybutyric acid, fengabine, cetylGABA, topiramate, tiagabine, acamprosate or a pharmaceutically acceptable salt thereof, or an enantiomer or a racemic mixture thereof.
- 55. The use according to Claim 53, wherein said medicament comprises gabapentin administered in an amount of about 500mg to about 2g/day.
- 56. The use according to Claim 53, wherein said medicament comprises valproic acid administered in an amount of about 5mg/kg to about 100 mg/kg/day.
- 57. The use according to Claim 53, wherein said medicament comprises topiramate administered in an amount of about 50mg to about 1g/day.
- 58. The use according to Claim 53, wherein said medicament comprises progabide administered in an amount of about 250mg to about 2g/day.
- 59. The use according to Claim 53, wherein said medicament comprises fengabine administered in an amount of about 250mg to about 4g/day.
- 60. The use according to Claim 53, wherein said medicament comprises gamma-hydroxybutyric acid administered in an amount of about 5mg/kg to about 100mg/kg/day.
- 61. The use according to Claim 53, wherein said psychostimulant, narcotic analgesic, alcohol or nicotine dependency characteristics are reduced in the absence of an aversive response or appetitive response to said medicament.
- 62. The use according to Claim 53, wherein said psychostimulant, narcotic analgesic, alcohol or nicotine dependency characteristics are reduced in the absence of an alteration in the locomotor function of said mammal.
- 63. Use of gamma vinylGABA (GVG) or a pharmaceutically acceptable salt thereof, or an enantiomer or a racemic mixture thereof, for preparing a medicament useful for changing addiction-related behavior of a mammal suffering from addiction to a combination of abused drugs by administering an effective amount of the medicament to the mammal, wherein the effective amount is sufficient to diminish, inhibit or eliminate behavior associated with craving or use of the combination of abused drugs.
- 64. The use according to Claim 63, wherein said elimination of behavior associated with craving the combination of abused drugs occurs in the absence of an aversive response or appetitive response to GVG.
- 65. The use according to Claim 63, wherein said combination of abused drugs is selected from the group consisting of psychostimulants, narcotic analgesics, alcohols and nicotine.
- 66. The use according to Claim 63, wherein said combination is selected from the group consisting of cocaine, nicotine, methamphetamine, ethanol, morphine and heroin.
- 67. The use according to Claim 63, wherein said combination is cocaine and heroin.
- 68. The use according to Claim 63, wherein GVG is administered in an amount of about 15mg/kg to about 600mg/kg.
- 69. The use according to Claim 63, wherein said addiction related behavior is conditioned place preference.
- 70. Use of gamma vinylGABA (GVG) or a pharmaceutically acceptable salt thereof, or an enantiomer or a racemic mixture thereof, for preparing a medicament useful for changing addiction-related behavior of a mammal suffering from addiction to a combination of abused drugs selected from the group consisting of psychostimulants, narcotic analgesics, alcohols and nicotine by administering an effective amount of the medicament to the mammal, wherein the effective amount attenuates the rewarding/incentive effects of the combination of abused drugs in the absence of altering rewarding/incentive effects of food in said mammal.
- 71. The use according to Claim 70, wherein said combination is selected from the group consisting of cocaine, nicotine, methamphetamine, ethanol, morphine and heroin.
- 72. The use according to Claim 70, wherein said combination is cocaine and heroin.
- 73. The use according to Claim 70, wherein the rewarding/incentive effects of the combination of abused drugs is attenuated in the absence of an alteration in the locomotor function of said mammal.
- 74. Use of gamma vinylGABA (GVG) or a pharmaceutically acceptable salt thereof, or an enantiomer or a racemic mixture thereof for preparing a medicament useful for ameliorating effects of addiction to a combination of abused drugs selected from the group consisting of psychostimulant, narcotic analgesic, alcohol and nicotine in a mammal by administering an effective amount of the medicament to the mammal, wherein the effective amount is sufficient to reduce dependency characteristics of the combination of abused drugs.
- 75. The use according to Claim 74, wherein said combination is selected from the group consisting of cocaine, nicotine, methamphetamine, ethanol, morphine and heroin.
- 76. The use according to Claim 74, wherein said combination is cocaine and heroin.
- 77. The use according to Claim 74, wherein GVG is administered in an amount from about 15mg/kg to about 600mg/kg.
- 78. The use according to Claim 74, wherein said dependency characteristics are reduced in the absence of an aversive response or appetitive response to GVG.
- 79. The use according to Claim 74, wherein said dependency characteristics are reduced in the absence of an alteration in the locomotor function of said mammal.
Applications Claiming Priority (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/129,253 US6057368A (en) | 1998-08-05 | 1998-08-05 | Treatment of addiction and addiction-related behavior |
US09/129,253 | 1998-08-05 | ||
US09/189,166 | 1998-11-09 | ||
US09/189,166 US6828349B1 (en) | 1998-08-05 | 1998-11-09 | Treatment of addiction and addiction-related behavior |
US09/209,952 | 1998-12-11 | ||
US09/209,952 US6541520B1 (en) | 1998-08-05 | 1998-12-11 | Treatment of addiction and addiction-related behavior |
PCT/US1999/017220 WO2000007583A2 (en) | 1998-08-05 | 1999-08-05 | Treatment of addiction and addiction-related behavior |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2339192A1 true CA2339192A1 (en) | 2000-02-17 |
CA2339192C CA2339192C (en) | 2009-12-22 |
Family
ID=27383860
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002339192A Expired - Fee Related CA2339192C (en) | 1998-08-05 | 1999-08-05 | Treatment of addiction and addiction-related behavior |
Country Status (24)
Country | Link |
---|---|
US (4) | US6541520B1 (en) |
EP (1) | EP1102583B1 (en) |
JP (1) | JP2002522383A (en) |
CN (1) | CN1172663C (en) |
AT (1) | ATE328588T1 (en) |
AU (1) | AU772715B2 (en) |
BR (1) | BR9912760A (en) |
CA (1) | CA2339192C (en) |
CY (1) | CY1105214T1 (en) |
CZ (1) | CZ2001394A3 (en) |
DE (1) | DE69931789T2 (en) |
DK (1) | DK1102583T3 (en) |
ES (1) | ES2267287T3 (en) |
HR (1) | HRP20010085A2 (en) |
HU (1) | HUP0103377A3 (en) |
ID (1) | ID28916A (en) |
IL (1) | IL141067A0 (en) |
MX (1) | MXPA01001268A (en) |
NO (1) | NO20010539L (en) |
NZ (1) | NZ509682A (en) |
PL (1) | PL198789B1 (en) |
PT (1) | PT1102583E (en) |
TW (1) | TWI243674B (en) |
WO (1) | WO2000007583A2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101203460B (en) * | 2005-05-17 | 2012-05-23 | Wm国际有限公司 | Apparatus and method for the non-chemical stabilization of bio-solids |
Families Citing this family (73)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6890951B2 (en) * | 1998-08-05 | 2005-05-10 | Brookhaven Science Associates Llc | Treatment of addiction and addiction-related behavior |
CA2341400A1 (en) * | 1998-08-25 | 2000-03-02 | Sepracor, Inc. | Methods and compositions employing optically pure s(+) vigabatrin |
JP2002527470A (en) * | 1998-10-20 | 2002-08-27 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | Anticonvulsant derivatives useful in the treatment of alcoholism, addiction and abuse |
BR0008477A (en) * | 1999-02-24 | 2002-01-22 | Univ Cincinnati | Method to treat an impulse control disorder |
MXPA01011014A (en) * | 1999-04-30 | 2003-06-30 | Johnson & Johnson | Anticonvulsant derivatives useful in treating cocaine dependency. |
IT1313585B1 (en) * | 1999-07-30 | 2002-09-09 | Neuroscienze S C A R L | USE OF GABAB RECEPTOR AGONISTS FOR THE MAINTENANCE THERAPY OF NICOTINE ABSTINENCE IN NICOTINO-EMPLOYEES. |
US6395783B1 (en) * | 2000-10-23 | 2002-05-28 | Brookhaven Science Associates, Llc | Treatment of PCP addiction and PCP addiction-related behavior |
US20050192271A1 (en) * | 2003-07-15 | 2005-09-01 | Hythiam, Inc. | Use of selective chloride channel modulators to treat alcohol and/or stimulant substance abuse |
US20020187996A1 (en) * | 2001-05-14 | 2002-12-12 | Dewey Stephen L. | Prevention of addiction in pain management |
US6462084B1 (en) * | 2001-05-14 | 2002-10-08 | Brookhaven Science Associates, Llc | Treatment for obsessive-compulsive disorder (OCD) and OCD-related disorders using GVG |
UA78211C2 (en) | 2001-07-09 | 2007-03-15 | Ortho Mcneil Pharm Inc | Salts of fructopyranose derivatives as anticonvulsant |
US7041650B2 (en) | 2001-07-09 | 2006-05-09 | Ortho-Mcneil Pharmaceutical, Inc. | Anticonvulsant derivative salts |
US20030068375A1 (en) | 2001-08-06 | 2003-04-10 | Curtis Wright | Pharmaceutical formulation containing gelling agent |
US7822470B2 (en) * | 2001-10-11 | 2010-10-26 | Osypka Medical Gmbh | Method for determining the left-ventricular ejection time TLVE of a heart of a subject |
US6559293B1 (en) | 2002-02-15 | 2003-05-06 | Transform Pharmaceuticals, Inc. | Topiramate sodium trihydrate |
US20100311701A1 (en) * | 2002-02-15 | 2010-12-09 | Transform Pharmaceuticals, Inc | Pharmaceutical Co-Crystal Compositions |
US7927613B2 (en) | 2002-02-15 | 2011-04-19 | University Of South Florida | Pharmaceutical co-crystal compositions |
US20090088443A1 (en) * | 2002-02-15 | 2009-04-02 | Julius Remenar | Novel crystalline forms of conazoles and methods of making and using the same |
US7790905B2 (en) | 2002-02-15 | 2010-09-07 | Mcneil-Ppc, Inc. | Pharmaceutical propylene glycol solvate compositions |
AU2003213719A1 (en) * | 2002-03-01 | 2003-09-16 | Regents Of The University Of Michigan | Multiple-component solid phases containing at least one active pharmaceutical ingredient |
US6797707B2 (en) * | 2002-03-29 | 2004-09-28 | University Of Florida | Antagonists of RF-amide neuropeptides |
US20070059356A1 (en) * | 2002-05-31 | 2007-03-15 | Almarsson Oern | Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothiazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen |
MXPA05000232A (en) | 2002-06-21 | 2005-06-17 | Transform Pharmaceuticals Inc | Pharmaceutical compositions with improved dissolution. |
US8183290B2 (en) | 2002-12-30 | 2012-05-22 | Mcneil-Ppc, Inc. | Pharmaceutically acceptable propylene glycol solvate of naproxen |
US20050043407A1 (en) * | 2003-08-22 | 2005-02-24 | Pfizer Inc | Pharmaceutical composition for the prevention and treatment of addiction in a mammal |
US7201920B2 (en) | 2003-11-26 | 2007-04-10 | Acura Pharmaceuticals, Inc. | Methods and compositions for deterring abuse of opioid containing dosage forms |
EP3326617A1 (en) | 2004-06-12 | 2018-05-30 | Collegium Pharmaceutical, Inc. | Abuse-deterrent drug formulations |
MY147767A (en) | 2004-06-16 | 2013-01-31 | Janssen Pharmaceutica Nv | Novel sulfamate and sulfamide derivatives useful for the treatment of epilepsy and related disorders |
US20070231268A1 (en) * | 2004-11-24 | 2007-10-04 | Acura Pharmaceuticals, Inc. | Methods and compositions for deterring abuse of orally administered pharmaceutical products |
US20060177380A1 (en) * | 2004-11-24 | 2006-08-10 | Acura Pharmaceuticals, Inc. | Methods and compositions for deterring abuse of orally administered pharmaceutical products |
US20080152595A1 (en) * | 2004-11-24 | 2008-06-26 | Acura Pharmaceuticals, Inc. | Methods and compositions for deterring abuse of orally administered pharmaceutical products |
US20060110327A1 (en) * | 2004-11-24 | 2006-05-25 | Acura Pharmaceuticals, Inc. | Methods and compositions for deterring abuse of orally administered pharmaceutical products |
US8283478B2 (en) | 2005-05-20 | 2012-10-09 | Janssen Pharmaceutica Nv | Process for preparation of sulfamide derivatives |
JP2009507081A (en) * | 2005-09-07 | 2009-02-19 | ブレインセルス,インコーポレイティド | Regulation of neurogenesis by HDac inhibition |
US20070134169A1 (en) * | 2005-12-11 | 2007-06-14 | Rabinoff Michael D | Methods for smoking cessation or alcohol cessation or other addiction cessation |
US8937096B2 (en) | 2005-12-19 | 2015-01-20 | Janssen Pharmaceutica Nv | Use of benzo-fused heterocyle sulfamide derivatives for the treatment of mania and bipolar disorder |
US8691867B2 (en) | 2005-12-19 | 2014-04-08 | Janssen Pharmaceutica Nv | Use of benzo-fused heterocycle sulfamide derivatives for the treatment of substance abuse and addiction |
US8492431B2 (en) | 2005-12-19 | 2013-07-23 | Janssen Pharmaceutica, N.V. | Use of benzo-fused heterocycle sulfamide derivatives for the treatment of obesity |
US8716231B2 (en) | 2005-12-19 | 2014-05-06 | Janssen Pharmaceutica Nv | Use of benzo-fused heterocycle sulfamide derivatives for the treatment of pain |
US8497298B2 (en) | 2005-12-19 | 2013-07-30 | Janssen Pharmaceutica Nv | Use of benzo-fused heterocycle sulfamide derivatives for lowering lipids and lowering blood glucose levels |
DE102006016990A1 (en) * | 2006-04-11 | 2007-10-18 | Hermann, Holger Lars, Dr. | Use of baclofen compounds to treat dependence on gamma-hydroxybutyrate or its analogs |
EA200870556A1 (en) | 2006-05-19 | 2009-06-30 | Янссен Фармацевтика Н.В. | COMBINED THERAPY IN THE TREATMENT OF EPILEPSY AND RELATED DISORDERS |
US20080103111A1 (en) * | 2006-06-21 | 2008-05-01 | Harlan Clayton Bieley | Smoking Cessation Treatment with Appetite Suppression |
US20100021570A1 (en) * | 2006-06-21 | 2010-01-28 | Harlan Clayton Bieley | Smoking Cessation Treatment By Reducing Nicotine Cravings, Apetite Suppression, And Altering The Perceived Taste Of Tobacco Smoke |
US20090239942A1 (en) * | 2006-09-15 | 2009-09-24 | Cloyd James C | Topiramate Compositions and Methods of Making and Using the Same |
PT2061458E (en) * | 2006-09-15 | 2015-03-11 | Univ Minnesota | Topiramate compositions and methods for their use |
US20090270438A1 (en) * | 2006-10-18 | 2009-10-29 | Clive Booles | Novel compositions and formulations |
JPWO2008090736A1 (en) * | 2007-01-23 | 2010-05-20 | 公立大学法人名古屋市立大学 | Medicament for the prevention and treatment of Alzheimer type dementia |
CN106983747A (en) | 2007-08-06 | 2017-07-28 | 生物系治疗公司 | The method for treating dependence |
US8883817B2 (en) * | 2007-10-18 | 2014-11-11 | Aiko Biotechnology | Combination analgesic employing opioid and neutral antagonist |
US8748448B2 (en) | 2007-10-18 | 2014-06-10 | Aiko Biotechnology | Combination analgesic employing opioid agonist and neutral antagonist |
PE20110060A1 (en) | 2008-06-23 | 2011-01-31 | Janssen Pharmaceutica Nv | CRYSTALLINE FORM OF (2S) - (-) - N- (6-CHLORO-2,3-DIHYDRO-BENZO [1,4] DIOXIN-2-ILMETHYL) -SULFAMIDE |
US8815939B2 (en) | 2008-07-22 | 2014-08-26 | Janssen Pharmaceutica Nv | Substituted sulfamide derivatives |
EP3064064A1 (en) * | 2009-09-30 | 2016-09-07 | Acura Pharmaceuticals, Inc. | Methods and compositions for deterring abuse |
CN102573821A (en) * | 2009-09-30 | 2012-07-11 | 哈兰·克莱顿·比利 | Smoking cessation with body weight maintenance and nutritional supplement |
US10668060B2 (en) | 2009-12-10 | 2020-06-02 | Collegium Pharmaceutical, Inc. | Tamper-resistant pharmaceutical compositions of opioids and other drugs |
WO2011106692A2 (en) * | 2010-02-25 | 2011-09-01 | Northwestern University | Methods of using (1s, 3s) -3-amino-4-difluoromethylenyl-1-cyclopentanoic acid |
US20120046232A1 (en) * | 2010-06-22 | 2012-02-23 | Medical University Of South Carolina | Compositions and methods for reducing relapse of addictive behavior |
EP2826468A1 (en) | 2010-12-22 | 2015-01-21 | Purdue Pharma L.P. | Encased tamper resistant controlled release dosage forms |
CN103327969A (en) | 2010-12-23 | 2013-09-25 | 普渡制药公司 | Tamper resistant solid oral dosage forms |
US20140072936A1 (en) * | 2012-09-07 | 2014-03-13 | Patrick D. Herron | Method of Tracking Consumption and Associated Effects |
EP3446685A1 (en) | 2012-11-30 | 2019-02-27 | Acura Pharmaceuticals, Inc. | Self-regulated release of active pharmaceutical ingredient |
KR101840526B1 (en) | 2013-02-05 | 2018-03-20 | 퍼듀 퍼머 엘피 | Tamper resistant pharmaceutical formulations |
US8652527B1 (en) | 2013-03-13 | 2014-02-18 | Upsher-Smith Laboratories, Inc | Extended-release topiramate capsules |
US9101545B2 (en) | 2013-03-15 | 2015-08-11 | Upsher-Smith Laboratories, Inc. | Extended-release topiramate capsules |
US10751287B2 (en) | 2013-03-15 | 2020-08-25 | Purdue Pharma L.P. | Tamper resistant pharmaceutical formulations |
CA2943728C (en) | 2014-03-26 | 2020-03-24 | Sun Pharma Advanced Research Company Ltd. | Abuse deterrent immediate release biphasic matrix solid dosage form |
EP3643355A1 (en) * | 2014-06-03 | 2020-04-29 | Pop Test Abuse Deterrent Technology LLC | Drug device configured for wireless communication |
US11103581B2 (en) | 2015-08-31 | 2021-08-31 | Acura Pharmaceuticals, Inc. | Methods and compositions for self-regulated release of active pharmaceutical ingredient |
WO2017222575A1 (en) | 2016-06-23 | 2017-12-28 | Collegium Pharmaceutical, Inc. | Process of making more stable abuse-deterrent oral formulations |
CN114903006A (en) * | 2021-02-09 | 2022-08-16 | 中国科学院脑科学与智能技术卓越创新中心 | Construction method and application of non-human primate substance addiction model |
CN117295710A (en) * | 2021-05-05 | 2023-12-26 | 思维医学股份有限公司 | MDMA enantiomer |
CN115386421A (en) * | 2022-06-23 | 2022-11-25 | 江苏华熙益能生物科技有限公司 | Tobacco essence, preparation method and application thereof |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3639607A (en) | 1970-11-02 | 1972-02-01 | Jack E Phillips | Method for treating the tobacco smoking habit |
US3960927A (en) | 1975-03-18 | 1976-06-01 | Richardson-Merrell Inc. | Olefinic derivatives of amino acids |
NZ194348A (en) * | 1979-07-26 | 1982-09-14 | Merrell Toraude & Co | Fluorinated methyl-beta-alanine derivatives and pharmaceutical compositions |
GB2133002B (en) | 1982-12-30 | 1986-01-29 | Merrell Toraude & Co | Process for preparing 4-amino-5-hexenoic acid |
GB8311804D0 (en) | 1983-04-29 | 1983-06-02 | Merrell Toraude & Co | Treatment of seizure disorders and pharmaceutical compositions |
US4595697A (en) | 1984-03-28 | 1986-06-17 | Merrell Dow Pharmaceuticals Inc. | Treatment of seizure disorders and pharmaceutical compositions useful therein |
US5189064A (en) * | 1985-07-22 | 1993-02-23 | Matrix Technologies, Inc. | Treatment of cocaine addiction |
DE3882712D1 (en) | 1987-10-07 | 1993-09-02 | Matrix Technologies Inc | PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OF COCOA ADDICTION. |
EP0509180A1 (en) * | 1991-04-18 | 1992-10-21 | Merrell Dow Pharmaceuticals Inc. | Use of GABA-T inhibitors for the treatment of schizophrenia and phencyclidine intoxication |
US5189026A (en) * | 1991-06-07 | 1993-02-23 | Fractal Laboratories, Inc. | Treatment of human diseases involving dysregulation or dysfunction of the nervous system |
GB9125615D0 (en) * | 1991-12-02 | 1992-01-29 | Wyeth John & Brother Ltd | Amines |
US5332736A (en) * | 1993-11-01 | 1994-07-26 | Ortho Pharmaceutical Corporation | Anti-convulsant aroyl aminoacylpyrroles |
US5824684A (en) * | 1997-02-21 | 1998-10-20 | Synapse Pharmaceuticals International, Inc. | Method for treating drug and alcohol addiction |
US5760049A (en) * | 1997-02-21 | 1998-06-02 | Synapse Pharmaceuticals International, Inc. | Method for controlling tobacco use and alleviating withdrawal symptoms due to cessation of tobacco use |
KR20010031470A (en) | 1997-10-28 | 2001-04-16 | 둘락 노먼 씨. | Method of reducing craving in mammals |
JP2002527470A (en) | 1998-10-20 | 2002-08-27 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | Anticonvulsant derivatives useful in the treatment of alcoholism, addiction and abuse |
BR0008477A (en) | 1999-02-24 | 2002-01-22 | Univ Cincinnati | Method to treat an impulse control disorder |
MXPA01011014A (en) | 1999-04-30 | 2003-06-30 | Johnson & Johnson | Anticonvulsant derivatives useful in treating cocaine dependency. |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
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CN101203460B (en) * | 2005-05-17 | 2012-05-23 | Wm国际有限公司 | Apparatus and method for the non-chemical stabilization of bio-solids |
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