Details for Patent: 9,808,460

Title:	Controlled release auris sensory cell modulator compositions and methods for the treatment of otic disorders
Abstract:	Disclosed herein are auris acceptable gel compositions containing a multiparticulate glutamate receptor antagonist, and methods for the treatment of otic diseases or conditions through intratympanic administration of the composition to an individual afflicted with an otic disease or condition.
Inventor(s):	Lichter; Jay (Rancho Santa Fe, CA), Trammel; Andrew M. (Olathe, KS), Piu; Fabrice (San Diego, CA), Ye; Qiang (San Diego, CA), Vollrath; Benedikt (San Diego, CA), Dellamary; Luis A. (San Marcos, CA), Lebel; Carl (Malibu, CA), Harris; Jeffrey P. (La Jolla, CA)
Assignee:	OTONOMY, INC. (San Diego, CA) THE REGENTS OF THE UNIVERSITY OF CALIFORNIA (Oakland, CA)
Filing Date:	May 15, 2015
Application Number:	14/713,944
Claims:	1. An intratympanic composition for use in the treatment of otic disorders by intratympanic administration on or near the round window membrane of the ear, the pharmaceutical composition comprising an auris acceptable gel and a multiparticulate non-microencapsulated glutamate receptor antagonist, wherein sustained release of the glutamate receptor antagonist into the cochlea occurs for a period of at least 3 days. 2. The composition of claim 1, wherein the auris acceptable gel is an auris acceptable hydrogel. 3. The composition of claim 1, wherein the auris acceptable gel has a gelation viscosity between about 15,000 cP and about 1,000,000 cP. 4. The composition of claim 1, wherein the auris acceptable gel is capable of being injected by an 18-31 gauge needle through the tympanic membrane. 5. The composition of claim 1, wherein the composition has a practical osmolarity of from about 150 mOsm/L to about 1000 mOsm/L. 6. The composition of claim 1, wherein the composition has a pH between 7.0 and 8.0. 7. The composition of claim 1, wherein the glutamate receptor antagonist is essentially in the form of micronized particles. 8. The composition of claim 1, wherein the glutamate receptor antagonist is 1-aminoadamantane; dextromethorphan; dextrorphan; ibogaine; ifenprodil; (S)-ketamine; (R)-ketamine; memantine; dizocilpine (MK-801); gacyclidine; traxoprodil; D-2-amino-5-phosphonopentanoic acid (D-AP5); 3-((.+-.)2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid (CPP); conantokin; 7-chlorokynurenate (7-CK); licostinel; nitrous oxide; phencyclidine; riluzole; tiletamine; aptiganel; remacimide; DCKA (5, 7-dichlorokynurenic acid); kynurenic acid; 1-aminocyclopropanecarboxylic acid (ACPC); AP7 (2-amino-7-phosphonoheptanoic acid); APV (R-2-amino-5-phosphonopentanoate); CPPene (3-[(R)-2-carboxypiperazin-4-yl]-prop-2-enyl-1-phosphonic acid); (+)-(1S,2S)-1-(4-hydroxy-phenyl)-2-(4-hydroxy-4-phenylpiperidino)-1-pro-p- anol; (1S,2S)-1-(4-hydroxy-3-methoxyphenyl)-2-(4-hydroxy-4-phenylpiperidin- o)-1-propanol; (3R,4S)-3-(4-(4-fluorophenyl)-4-hydroxypiperidin-1-yl-)-chroman-4,7-diol; (1R*, 2R*)-1-(4-hydroxy-3-methylphenyl)-2-(4-(4-fluoro-phenyl)-4-hydroxyp- iperidin-1-yl)-propan-1-ol-mesylate; or a salt thereof or combinations thereof. 9. The composition of claim 1, wherein the glutamate receptor antagonist is an NMDA receptor antagonist. 10. The composition of claim 9, wherein the NMDA receptor antagonist is gacyclidine. 11. The composition of claim 9, wherein the NMDA receptor antagonist is an arylcycloalkylamine or a quinazoline. 12. The composition of claim 9, wherein the NMDA receptor antagonist is (S)-ketamine or a salt thereof. 13. The composition of claim 9, wherein the NMDA receptor antagonist is 7-CK or a salt thereof. 14. The composition of claim 1, wherein sustained release of the glutamate receptor antagonist into the cochlea occurs for a period of at least 5 days. 15. The composition of claim 1, wherein sustained release of the glutamate receptor antagonist into the cochlea occurs for a period of at least 10 days. 16. The composition of claim 1, wherein the otic disorder is tinnitus. 17. The composition of claim 1, wherein the composition provides a practical osmolarity from 250 mOsm/L to 320 mOsm/L.