US2018085349A1PendingUtilityA1

Stable preservative-free mydriatic and anti-inflammatory solutions for injection

Assignee: OMEROS CORPPriority: Oct 24, 2012Filed: Nov 27, 2017Published: Mar 29, 2018
Est. expiryOct 24, 2032(~6.2 yrs left)· nominal 20-yr term from priority
A61P 41/00A61P 27/04A61P 29/00A61P 27/08A61P 27/02A61K 31/407A61K 31/138A61K 9/0048A61K 31/137A61K 47/08A01N 43/48
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Claims

Abstract

The present invention relates to stable, preservative- and antioxidant-free liquid formulations of phenylephrine and ketorolac for injection.

Claims

exact text as granted — not AI-modified
The embodiments of the invention in which an exclusive property or privilete is claimed are defined as follows: 
     
         1 . A liquid pharmaceutical dosage form comprising phenylephrine, ketorolac, a buffer system, an intraocular irrigation carrier and an inter-gas overlay in a single-use container, wherein the phenylephrine is included at a concentration of from 30 to 720 μM and the ketorolac is included at a concentration of from 10 to 270 μM. 
     
     
         2 . The dosage form of  claim 1 , wherein the phenylephrine is included at a concentration of from 90 to 720 μM and the ketorolac is included at a concentration of from 44 to 134 μM. 
     
     
         3 . The dosage form of  claim 1 , wherein dosage form is stable for a period of at least 24 months when stored at a temperature of from 5+/−3° C. to 25+/−2° C. 
     
     
         4 . The dosage form of  claim 1 , wherein the dosage form is preservative-free and antioxidant-free. 
     
     
         5 . The dosage form of  claim 4 , wherein dosage form is stable for a period of at least 24 months when stored at a temperature of from 5+/−3° C. to 25+/−2° C. 
     
     
         6 . The dosage form of  claim 1 , wherein the buffer system is selected from a sodium phosphate buffer system and a sodium citrate buffer system. 
     
     
         7 . The dosage form of  claim 6 , wherein the buffer system comprises a sodium citrate buffer system. 
     
     
         8 . The dosage form of  claim 7 , wherein the buffer system comprises an about 20 mM sodium citrate buffer system. 
     
     
         9 . The dosage form of  claim 1 , wherein the dosage form has a pH of from 5.8 to 6.8.

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