Compositions for affecting weight loss
Abstract
Disclosed are compositions for affecting weight loss comprising a first compound and a second compound, where the first compound is an opioid antagonist and the second compound causes increased agonism of a melanocortin 3 receptor (MC3-R) or a melanocortin 4 receptor (MC4-R) compared to normal physiological conditions. Also disclosed are methods of affecting weight loss, increasing energy expenditure, increasing satiety in an individual, or suppressing the appetite of an individual, comprising identifying an individual in need thereof and treating that individual to antagonize opioid receptor activity and to enhance α-MSH activity.
Claims
exact text as granted — not AI-modified1 . A composition for affecting weight loss comprising a first compound and a second compound, wherein said first compound is a μ-opioid antagonist and said second compound is selected from the group consisting of a dopamine reuptake inhibitor, a norepinephrine reuptake inhibitor, a mixed dopamine/norepinephrine reuptake inhibitor, a dopamine agonist, a norepinephrine agonist, and a norepinephrine releaser.
2 . The composition of claim 1 , wherein said μ-opioid antagonist is selected from the group consisting of alvimopan, nalmefene, naloxone, naltrexone, methylnaltrexone, nalorphine, and pharmaceutically acceptable salts thereof.
3 . The composition of claim 2 , wherein said first compound is naltrexone or pharmaceutically acceptable salt thereof.
4 . The composition of claim 3 , wherein said second compound is a norepinephrine reuptake inhibitor.
5 . The composition of claim 4 , wherein said second compound is selected from the group consisting of bupropion, thionisoxetine, reboxetine, and pharmaceutically acceptable salts thereof.
6 . The composition of claim 1 , wherein said second compound is a norepinephrine reuptake inhibitor.
7 . The composition of claim 6 , wherein said second compound is selected from the group consisting of bupropion, thionisoxetine, reboxetine, and pharmaceutically acceptable salts thereof.
8 . The composition of claim 2 , wherein said second compound is selected from the group consisting of bupropion, thionisoxetine, reboxetine, and pharmaceutically acceptable salts thereof.
9 . The composition of claim 1 , wherein said first compound is naltrexone or pharmaceutically acceptable salt thereof, and said second compound is bupropion or pharmaceutically acceptable salt thereof.
10 . The composition of claim 9 , wherein said composition is a sustained release composition.
11 . The composition of claim 9 , wherein said second compound is sustained release bupropion.
12 . A pharmaceutical composition for affecting weight loss comprising a first compound, a second compound, and a carrier or excipient, wherein said first compound is a μ-opioid antagonist and said second compound is selected from the group consisting of a dopamine reuptake inhibitor, a norepinephrine reuptake inhibitor, a mixed dopamine/norepinephrine reuptake inhibitor, a dopamine agonist, a norepinephrine agonist, and a norepinephrine releaser.
13 . The pharmaceutical composition of claim 12 , wherein said μ-opioid antagonist is selected from the group consisting of alvimopan, nalmefene, naloxone, naltrexone, methylnaltrexone, nalorphine, and pharmaceutically acceptable salts thereof.
14 . The pharmaceutical composition of claim 13 , wherein said first compound is naltrexone or pharmaceutically acceptable salt thereof.
15 . The pharmaceutical composition of claim 14 , wherein said second compound is a norepinephrine reuptake inhibitor.
16 . The pharmaceutical composition of claim 15 , wherein said second compound is selected from the group consisting of bupropion, thionisoxetine, reboxetine, and pharmaceutically acceptable salts thereof.
17 . The pharmaceutical composition of claim 12 , wherein said second compound is a norepinephrine reuptake inhibitor.
18 . The pharmaceutical composition of claim 17 , wherein said second compound is selected from the group consisting of bupropion, thionisoxetine, reboxetine, and pharmaceutically acceptable salts thereof.
19 . The pharmaceutical composition of claim 13 , wherein said second compound is selected from the group consisting of bupropion, thionisoxetine, reboxetine, and pharmaceutically acceptable salts thereof.
20 . The pharmaceutical composition of claim 12 , wherein said first compound is naltrexone or pharmaceutically acceptable salt thereof, and said second compound is bupropion or pharmaceutically acceptable salt thereof.Join the waitlist — get patent alerts
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