US2001025038A1PendingUtilityA1
Method of reducing craving in mammals
Priority: Oct 28, 1997Filed: May 1, 2001Published: Sep 27, 2001
Est. expiryOct 28, 2017(expired)· nominal 20-yr term from priority
A61K 31/47A61K 31/55
49
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Claims
Abstract
A method of reducing cravings in a mammal to food or an addictive substance is disclosed. The method comprises administering to the mammal an effective amount of a D 1 /D 5 antagonist or a D 1 /D 5 partial agonist alone or in combination with other specified CNS compounds.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for reducing cravings to food or an addictive substance in a mammal comprising administering to the mammal an anti-craving effective amount of a D 1 /D 5 antagonist, a D 1 /D 5 partial agonist or mixtures thereof.
2 . The method of claim 1 wherein the D 1 /D 5 antagonist or D 1 /D 5 partial agonist is administered at a daily dosage range of about 0.01 to about 500 mg/kg.
3 . The method of claim 2 wherein the D1/D5 antagonist is administered at a daily dosage range of about 1 to about 150 mg/kg.
4 . The method of claim 2 wherein the addictive substance is cocaine, amphetamine, nicotine, opiates, tobacco or alcohol.
5 . The method of claim 4 wherein the D 1 /D 5 antagonist is selected from the class consisting of SCH39166, SCH23390, BTS-73-947, NNC-22-0010, JHS-271, JHS-198, JHS-136 and A69024, and the D 1 /D 5 partial agonist is SKF 38393.
6 . The method of claim 5 wherein the D 1 /D 5 antagonist is SCH 39166.
7 . The method of claim 6 wherein the substance craved is food.
8 . The method of claim 7 further comprising the administration of a compound selected from the class consisting of sibutramine, fluoxitine, fenfluramine and analogs, amphetamine and analogs, phenteramine, diethylproprion and mazindol.
9 . The method of claim 6 wherein the substance craved is nicotine.
10 . The method of claim 9 further comprising the administration of a compound selected from the class consisting of buspirone and buproprion.
11 . The method of claim 6 wherein the substance craved is alcohol.
12 . The method of claim 11 further comprising the administration of a compound selected from the class consisting of disulfiram, acamprosate and naltrexone.
13 . A method for reducing cravings to food or an addictive substance in a mammal comprising administering to the mammal an anti-craving effective amount of a compound selected from a D 1 /D 5 antagonist, a D 1 /D 5 partial agonist and mixtures thereof, and a compound selected from the class consisting of:
A. anti-obesity compounds; B. serotonin receptor agonists and antagonists; C. antipsychotics/anxiolytics; D. antidepressants; E. dopaminergic agonists; F. anticonvulsants/mood stimulants; G. cocaine-like agonists; H. cocaine catalytic antibodies; and I. alcohol antagonist drugs.
14 . The method of claim 13 wherein the D 1 /D 5 antagonist is selected from the class consisting of SCH39166, SCH23390, BTS-73-947, NNC-22-0010, JHS-271, JHS-198, JHS-136 and A-69024.
15 . The method of claim 14 wherein the D 1 /D 5 antagonist is SCH39166.
16 . A method for reducing food cravings in a mammal comprising administering to the mammal an anti-craving effective amount of SCH 39166.
17 . A method for reducing nicotine cravings in a mammal comprising administering to the mammal an anti-craving effective amount of SCH 39166.
18 . A method for reducing alcohol cravings in a mammal comprising administering to the mammal an anti-craving effective amount of SCH 39166
19 . A kit to reduce cravings to food or an addictive substance comprising a compound selected from the class consisting of a D 1 /D 5 antagonist, a D 1 /D 5 partial agonist and mixtures thereof in combination with one or more compounds selected from the class consisting of:
A. anti-obesity compounds; B. serotonin receptor agonists and antagonists; C. antipsychotics/anxiolytics; D. antidepressants; E. dopaminergic agonists; F. anticonvulsants/mood stimulants; G. cocaine-like agonists; H. cocaine catalytic antibodies; and I. alcohol antagonist drugs.
20 . The kit of claim 19 wherein the D 1 /D 5 antagonist is SCH39166.Join the waitlist — get patent alerts
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