Controlled-Release CNS Modulating Compositions and Methods for the Treatment of Otic Disorders

Abstract

Disclosed herein are compositions and methods for the treatment of otic disorders with CNS modulating agent compositions and compositions administered locally to an individual afflicted with an otic disorder, through direct application of these compositions and compositions onto or via perfusion into the targeted auris structure(s).

1 .- 20 . (canceled) 
     
     
         21 . An intratympanic composition for use in the treatment of an otic disease or condition by administration on or near the round window membrane of the ear, the intratympanic composition comprising
 a multiparticulate Central Nervous System (CNS) modulator, or pharmaceutically acceptable salt thereof; and   an auris acceptable gel,   wherein the multiparticulate Central Nervous System (CNS) modulator, or pharmaceutically acceptable salt thereof is not provided as polymer-containing particles, and is suspended in the auris acceptable gel.   
     
     
         22 . The intratympanic composition of  claim 21 , wherein the auris acceptable gel is an auris acceptable hydrogel. 
     
     
         23 . The intratympanic composition of  claim 21 , wherein the auris acceptable gel has a gelation viscosity between about 15,000 cP and about 1,000,000 cP. 
     
     
         24 . The intratympanic composition of  claim 21 , wherein the auris acceptable gel is capable of being injected by a narrow gauge needle or cannula through the tympanic membrane to an area on or near the round window membrane. 
     
     
         25 . The intratympanic composition of  claim 21 , wherein the intratympanic composition has an osmolarity of from about 150 mOsm/L to about 1000 mOsm/L. 
     
     
         26 . The intratympanic composition of  claim 21 , wherein the multiparticulate Central Nervous System (CNS) modulator is micronized Central Nervous System (CNS) modulator. 
     
     
         27 . The intratympanic composition of  claim 21 , wherein the intratympanic composition has a pH between 7.0 and 8.0. 
     
     
         28 . The intratympanic composition of  claim 21 , wherein the CNS modulator is a GABA receptor modulator or an antihistamine. 
     
     
         29 . The intratympanic composition of  claim 28 , wherein the antihistamine is selected from meclizine, diphenhydramine, dimenhydrinate, loratadine, quetiapine, mepyramine, piperoxan, antazoline, carbinoxamine, doxylamine, clemastine, pheniramine, chlorphenamine, chlorpheniramine, dexchlorpheniramine, brompheniramine, triprolidine, cyclizine, chlorcyclizine, hydroxyzine, promethazine, alimemazine, trimeprazine, cyproheptadine, azatadine, ketotifen, oxatomide and betahistine. 
     
     
         30 . The intratympanic composition of  claim 28 , wherein the GABA receptor modulator agonizes the activity of a GABA receptor. 
     
     
         31 . The intratympanic composition of  claim 28 , wherein the GABA receptor modulator partially or fully inhibits the repolarization of a neuron. 
     
     
         32 . The intratympanic composition of  claim 28 , wherein the GABA receptor modulator is selected from a benzodiazepine, a loop diuretic, or a GABA analogue. 
     
     
         33 . The intratympanic composition of  claim 28 , wherein the GABA receptor modulator is selected from alprazolam, bromazepam, brotizolam, chlordiazepoxide, clonazepam, clorazepate, diazepam, estazolam, flunitrazepam, flurazepam, loprazolam, lorazepam, lormetazepam, idazolam, nimetazepam, nitrazepam, oxazepam, prazepam, temazepam, and triazolam or combinations thereof. 
     
     
         34 . The intratympanic composition of  claim 21 , wherein the otic disease or condition is endolymphatic hydrops, kinetosis, labyrinthitis, mal de debarquement, Meniere's disease, Meniere's syndrome, Ramsay Hunt's syndrome (Herpes zoster infection), recurrent vestibulopathy, tinnitus, vertigo, microvascular compression syndrome, utricular dysfunction, vestibular neuronitis, benign paroxysmal positional vertigo, or combinations thereof. 
     
     
         35 . The intratympanic composition of  claim 21 , wherein the otic disease or condition is tinnitus. 
     
     
         36 . The intratympanic composition of  claim 21 , wherein sustained release of the CNS modulator into the cochlea occurs for a period of at least 5 days after a single administration. 
     
     
         37 . The intratympanic composition of  claim 21 , wherein sustained release of the CNS modulator into the cochlea occurs for a period of at least 10 days after a single administration.