US2012122874A1PendingUtilityA1

Combination of a sedative and a neurotransmitter modulator, and methods for treating depression

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Assignee: LALJI KARIMPriority: Dec 11, 2003Filed: Nov 28, 2011Published: May 17, 2012
Est. expiryDec 11, 2023(expired)· nominal 20-yr term from priority
A61P 43/00A61P 25/24A61P 25/20A61K 45/06A61K 31/724A61K 31/137A61K 31/138A61K 31/4985A61K 31/495
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Claims

Abstract

One aspect of the present invention relates to pharmaceutical compositions containing two or more active agents that when taken together can be used to treat, e.g., insomnia and/or depression. The first component of the pharmaceutical composition is a GABA receptor modulating compound. The second component of the pharmaceutical composition is a serotonin reuptake inhibitor, a norepinephrine reuptake inhibitor, a 5-HT 2A modulator, or dopamine reuptake inhibitor. In certain embodiments, the pharmaceutical composition comprises eszopiclone. In a preferred embodiment, the pharmaceutical composition comprises eszopiclone and fluoxetine. The present invention also relates to a method of treating a sleep abnormality, treating insomnia, treating depression, augmenting antidepressant therapy, eliciting a dose-sparing effect, reducing depression relapse, improving the efficacy of antidepressant therapy or improving the tolerability of antidepressant therapy, comprising co-administering to a patient in need thereof a GABA-receptor-modulating compound; and a SRI, NRI, 5-HT 2A modulator or DRI.

Claims

exact text as granted — not AI-modified
1 .- 36 . (canceled) 
     
     
         37 . An improved method of antidepressant therapy utilizing a serotonin reuptake inhibitor, the improvement comprising administering a therapeutically effective amount of eszopiclone, or a pharmaceutically acceptable salt thereof, thereby accomplishing one or more outcomes selected from the group consisting of augmenting antidepressant response, eliciting a dose sparing effect, reducing depression relapse, improving efficacy of the antidepressant therapy, and improving tolerability of the antidepressant therapy. 
     
     
         38 . The method of  claim 37 , wherein the outcome comprises augmenting antidepressant response. 
     
     
         39 . The method of  claim 37 , wherein the outcome comprises eliciting a dose sparing effect. 
     
     
         40 . The method of  claim 37 , wherein the outcome comprises reducing depression relapse. 
     
     
         41 . The method of  claim 37 , wherein the outcome comprises improving efficacy of the antidepressant therapy. 
     
     
         42 . The method of  claim 37 , wherein the outcome comprises improving tolerability of the antidepressant therapy. 
     
     
         43 . The method of  claim 37 , wherein the serotonin reuptake inhibitor is norsertraline.

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