IP Library Granted Patent US 9,993,471
Granted Patent B2
US 9,993,471 · App. 15/456,249 · Granted Jun 12, 2018

Ophthalmic formulations of cetirizine and methods of use

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Quick Facts
Patent No.
US 9,993,471
App. No.
15/456,249
Granted
Jun 12, 2018
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 (6)

1. A method for the treatment of the signs and symptoms of allergic conjunctivitis comprising topically administering to an eye of a subject in need thereof a topical ophthalmic formulation comprising 0.1% to 0.25% (w/v) cetirizine hydrochloride or dihydrochloride, wherein cetirizine is the only active agent in the formulation and the formulation is formulated in a vehicle comprising 1% Polyethylene Glycol 400, NF, 0.2% Dibasic Sodium Phosphate, Anhydrous, USP, 0.25% Hypromellose, USP, 0.1% Polysorbate 80, NF, 1.2% to 1.8% Glycerin, USP, 0.025% Edetate disodium, USP; 0.01% Benzalkonium Chloride, NF, and Purified Water, USP, wherein the formulation has a pH 7 and does not contain a cyclodextrin or other solubilizing compound.

2. The method of claim 1 , wherein the signs and symptoms are ocular itching, ocular redness and lid swelling and associated nasal symptoms.

3. A method for the treatment of the signs and symptoms of allergic conjunctivitis comprising topically administering to an eye of a subject in need thereof a topical ophthalmic formulation consisting of 0.1% (w/v) cetirizine, 1% Polyethylene Glycol 400, NF, 0.2% Dibasic Sodium Phosphate, Anhydrous, USP, 0.25% Hypromellose, USP, 0.1% Polysorbate 80, NF, 1.8% Glycerin, USP, 0.025% Edetate disodium, USP; 0.025% Edetate disodium, 0.01% Benzalkonium Chloride, NF, and Purified Water, USP and wherein the formulation has a pH 7 and does not contain a cyclodextrin or other solubilizing compound.

4. The method according to claim 3 wherein the cetirizine is present as cetirizine hydrochloride or dihydrochloride.

5. The method according to claim 3 , wherein the signs and symptoms are ocular itching, ocular redness and lid swelling and associated nasal symptoms.

6. The method according to claim 4 , wherein the signs and symptoms are ocular itching, ocular redness and lid swelling and associated nasal symptoms.

Assignments (4)
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS Recorded Oct 9, 2020
From: HAYFIN SERVICES LLP
To: EYEVANCE PHARMACEUTICALS LLC
Reel/Frame 054172/0632 →
SECURITY INTEREST Recorded Oct 17, 2019
From: EYEVANCE PHARMACEUTICALS LLC, AS GRANTOR
To: HAYFIN SERVICES LLP, AS COLLATERAL AGENT
Reel/Frame 050751/0051 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 14, 2017
From: ABELSON, MARK BARRY; CHAPIN, MATTHEW JONATHAN; GOMES, PAUL; MINNO, GEORGE; NICE, JACKIE
To: ACIEX THERAPEUTICS, INC.
Reel/Frame 043008/0539 →
CHANGE OF NAME Recorded Jul 14, 2017
From: ACIEX THERAPEUTICS, INC.
To: NICOX OPHTHALMICS, INC.
Reel/Frame 043202/0908 →