Details for Patent: 9,511,020

Title:	Controlled release corticosteroid compositions and methods for the treatment of otic disorders
Abstract:	Disclosed herein are compositions and methods for the treatment of otic disorders with steroid, NSAID, and/or adenosine triphosphatase ("ATPase") modulator agents. In these methods, the steroidal, NSAID, and/or ATPase compositions and formulations are administered locally to an individual afflicted with an otic disorder, through direct application of these compositions and formulations onto or via perfusion into the targeted auris structure(s).
Inventor(s):	Lichter; Jay (Rancho Santa Fe, CA), Trammel; Andrew M. (Olathe, KS), Piu; Fabrice (San Diego, CA), Ye; Qiang (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:	Jul 09, 2015
Application Number:	14/795,819
Claims:	1. A method of ameliorating an inner ear disease or disorder in a patient in need thereof comprising injecting through the tympanic membrane into the middle ear cavity of the patient a controlled release composition comprising dexamethasone and a thermosetting polymer; wherein the dexamethasone is uncoated and is suspended in the composition, and the thermosetting polymer is poloxamer 407 at a concentration of at least 10% w/w and up to 20% w/w, and wherein a single dose of the controlled release composition in the syringe is from 300 .mu.L to 500 .mu.L. 2. The method of claim 1, wherein the controlled release composition provides controlled release of the pharmaceutical agent for an extended period of time of one or more days. 3. The method of claim 1, wherein the controlled release composition is a suspension in which the pharmaceutically active agent is dispersed within the thermosetting polymer. 4. The method of claim 1, wherein the controlled release composition further comprises a phosphate which buffers the pH of the controlled release composition to about 7.4. 5. The method of claim 1, wherein the controlled release composition is contained in a syringe optionally connected to a needle. 6. The method of claim 1, wherein the inner ear disease or disorder is selected from the group consisting of tinnitus, hearing loss, vertigo, Meniere's disease, autoimmune disorders, and inner ear infections and inflammations. 7. The method of claim 1, wherein the inner ear disease or disorder is Meniere's disease. 8. The method of claim 1, wherein the thermosetting polymer has a gelation temperature of between about 12.degree. C. to about 20.degree. C.