IP Library Granted Patent US 11,918,573
Granted Patent B2
US 11,918,573 · App. 17/332,814 · Granted Mar 5, 2024

Ophthalmic formulations of cetirizine and methods of use

Inventors: Mark Barry Abelson (Andover, MA); Matthew J. Chapin (Amesbury, MA); Paul Gomes (Andover, MA); George Minno (Windham, NH); Jackie Nice (Medford, MA)
Assignee: NICOX OPHTHALMICS, INC.
A61K31/495A61K9/0048A61K9/08A61K31/4174A61K31/4965A61K31/56A61K31/569A61K47/02A61K47/10A61K47/26A61K47/38
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Quick Facts
Patent No.
US 11,918,573
App. No.
17/332,814
Granted
Mar 5, 2024
Kind
B2
Abstract

The present invention provides stable topical formulations of cetirizine that provide a comfortable formulation when instilled in the eye and is effective in the treatment of allergic conjunctivitis and/or allergic conjunctivitis. The invention further provides methods of treating allergic conjunctivitis and/or allergic rhinoconjunctivitis in a subject in need of such treatment by topical application of the cetirizine formulations of the invention directly to the eye.

Claims (11)

1. A topical ophthalmic formulation comprising cetirizine hydrochloride or dihydrochloride in an amount of 0.05% to 0.5% (w/v) calculated as cetirizine free base, wherein cetirizine is the only active agent in the formulation and the cetirizine is formulated in a vehicle comprising (a) a demulcent and/or viscosity enhancing polymer, (b) a preservative and (c) a surfactant comprising a polysorbate at a concentration of 0.02 to 0.1% (w/v), (d) a carrier comprising polyethylene glycol, and (e) water, wherein the formulation has a pH of about 5.5 to 7.5, a viscosity of from 1-50 centipoise and an osmolality of about 225-400 mOsm/kg, and wherein the formulation does not contain a cyclodextrin.

2. The topical ophthalmic formulation of claim 1 , wherein the cetirizine hydrochloride or dihydrochloride is present in an amount of 0.1% to 0.25% (w/v) calculated as cetirizine free base.

3. The topical ophthalmic formulation of claim 1 , wherein the formulation has an osmolality of 280-320 mOsm/kg.

4. The topical ophthalmic formulation of claim 1 , wherein the formulation has a pH of about 6.0 to 7.0.

5. The topical ophthalmic formulation of claim 1 , wherein the preservative comprises benzalkonium chloride.

6. The topical ophthalmic formulation of claim 1 , wherein the viscosity is from 5-30 centipoise.

7. The topical ophthalmic formulation of claim 1 , wherein the demulcent and/or viscosity enhancing polymer comprises one or more members selected from the group consisting of a cellulose derivative, dextran, gelatin, a polyol and a carbomer.

8. The topical ophthalmic formulation of claim 7 , wherein the cellulose derivative comprises one or more members selected from the group consisting of carboxymethycellulose, hydroxyethylcellulose, hydroxypropyl methylcellulose and methylcellulose.

9. The topical ophthalmic formulation of claim 7 , wherein the polyol comprises one or more members selected from the group consisting of glycerin, propylene glycol, polyvinyl alcohol and povidone.

10. The topical ophthalmic formulation of claim 1 , wherein the formulation further comprises a chelating agent.

11. The topical ophthalmic formulation of claim 10 , wherein the chelating agent comprises edetate disodium.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 29, 2021
From: ABELSON, MARK BARRY; CHAPIN, MATTHEW JONATHAN; GOMES, PAUL; MINNO, GEORGE; NICE, JACKIE
To: ACIEX THERAPEUTICS, INC.
Reel/Frame 058503/0074 →
CHANGE OF NAME Recorded Dec 29, 2021
From: ACIEX THERAPEUTICS, INC.
To: NICOX OPHTHALMICS, INC.
Reel/Frame 058767/0284 →
Continuity (9)
Continuation 17018865 · Sep 11, 2020
Continuation 16839954 · Apr 3, 2020
Division 16001679 · Jun 6, 2018
Continuation 15456249 · Mar 10, 2017
Continuation 14982258 · Dec 29, 2015
Continuation 12724128 · Mar 15, 2010
Provisional Application 61174850 · May 1, 2009
Provisional Application 61161006 · Mar 17, 2009
Related Publication 20210290617A1 · Sep 23, 2021