US2019192465A1PendingUtilityA1

METHODS OF TREATING CHRONIC DRY EYE DISEASE USING C16:1n7-PALMITOLEATE AND DERIVATIVES THEREOF

Assignee: TERSUS LIFE SCIENCES LLCPriority: Jun 4, 2014Filed: Jul 20, 2018Published: Jun 27, 2019
Est. expiryJun 4, 2034(~7.8 yrs left)· nominal 20-yr term from priority
A61P 27/02A61K 45/06A61K 31/201A61K 31/20A61K 31/231A61K 31/23A61K 38/13A61K 31/717
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Claims

Abstract

The present technology provides methods for preventing or treating dry eyes in a subject in need thereof. The methods include administering to the subject an effective amount of a composition comprising C16:1n7-palmitoleate, its derivatives, pharmaceutically acceptable salts thereof, or a combination thereof.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method for preventing or treating dry eyes in a subject in need thereof comprising administering to the subject an effective amount of a composition comprising one or more of C16:1n7-palmitoleate, a C16:1n7-palmitoleate derivative, a pharmaceutically acceptable salt thereof, or a combination thereof. 
     
     
         2 . The method of  claim 1 , wherein the composition further comprises a C16:0-palmitate, a C16:0-palmitate derivative, or a combination thereof. 
     
     
         3 . The method of  claim 1 , wherein the composition further comprises a C18:1n9-oleate, a C18:1n9-oleate derivative, or a combination thereof. 
     
     
         4 . The method of  claim 1 , wherein the subject has been diagnosed with dry eyes or dry eye syndrome. 
     
     
         5 . The method of  claim 1 , wherein the subject is at risk for dry eyes or dry eye syndrome. 
     
     
         6 . The method of  claim 5 , wherein the subject is human. 
     
     
         7 . The method of  claim 1 , further comprising simultaneously, sequentially, or separately administrating at least one additional therapeutic agent, wherein the at least one additional therapeutic agent, is selected from the group consisting of cyclosporine ophthalmic emulsion, antibiotics, and hydroxypropyl cellulose insert. 
     
     
         8 . The method of  claim 1 , wherein the composition is administered orally, topically, systemically, intravenously, subcutaneously, intraperitoneally, or intramuscularly. 
     
     
         9 . The method of  claim 1 , wherein administration of the composition prevents, treats, or ameliorates one or more signs and/or symptoms of dry eyes. 
     
     
         10 . The method of  claim 9 , wherein the signs and/or symptoms are selected from the group consisting of stinging, burning, or scratchy sensation in the eyes, stringy mucus in or around the eyes, increased eye irritation from smoke or wind, eye fatigue, sensitivity to light, eye redness, sensation of foreign object in eyes, difficulty wearing contact lenses, periods of excessive tearing, swollen eyes, eye discomfort, eye pain, and blurred vision. 
     
     
         11 . The method of  claim 1 , wherein the subject displays tear osmolarity less than 308 mOsms/L. 
     
     
         12 . The method of  claim 1 , wherein the composition is administered daily for 4 weeks or more.

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