Ophthalmic Composition For The Treatment Of Ocular Infection

US2017196805A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2017196805-A1
Application numberUS-201515314137-A
CountryUS
Kind codeA1
Filing dateJun 18, 2015
Priority dateJun 20, 2014
Publication dateJul 13, 2017
Grant date

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

An ophthalmic composition for administration to an eye of a patient for the treatment of an ocular infection. The ophthalmic composition contains an ε-polylysine (εPL) in an amount effective to treat or control or prevent the ocular infection.

First claim

Opening claim text (preview).

1 . An ophthalmic composition for use in the treatment of an ocular infection when the ophthalmic composition is administered to an eye of a patient, or the prophylaxis of an ocular infection when the ophthalmic composition is administered to an eye of a patient before or after the introduction of an inoculum of an ocular pathogen, said composition comprising an amount of ε-polylysine (εPL) effective for said treatment. 2 . The composition for use of claim 1 , wherein the ocular infection is bacterial conjunctivitis. 3 . The composition for use of claim 1 , wherein the ocular infection is bacterial keratitis. 4 . (canceled) 5 . The composition for use of claim 1 , wherein the ocular infection is bacterial endophthalmitis. 6 . The composition for use of claim 1 , wherein the ocular infection is caused by a methicillin-resistant Staphylococus aureus (MRSA). 7 . The composition for use of any preceding claim 1 , wherein the amount of εPL is between 0.001 and 2.0 percent by weight. 8 . The composition for use of claim 1 further comprising a viscosity-increasing agent. 9 . The composition for use of claim 1 further comprising a mucoadhesive agent. 10 . The composition for use of claim 1 further comprising an excipient that is a polyvinyl alcohol, polypropylene glycol, a carbomer, polycarbophil, a polyoxyethlene-polyoxypropylene block copolymer, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, carboxymethyl cellulose, hydroxyethyl cellulose, hyaluronic acid, dextran, chondroitin sulfate, gellan gum, xanthan gum, guar gum, trehalose, tamarind seed polysaccharide, or a cyclodextrin, or any combinations of any two or more of the foregoing excipients. 11 . The composition for use of claim 1 , wherein the composition comprises no preservative agent in addition to the ε-polylysine (εPL). 12 . The composition for use of claim 1 , wherein the composition is formulated as a liquid for administering by one or more drops to the eye. 13 . The composition for use of claim 1 , wherein the composition is formulated as a unit dose ocular insert for placement in the eye's cul de sac. 14 . An eye drop dispensing bottle comprising in liquid form, the ophthalmic composition for use in the treatment of prophylaxis of an ocular infection of claim 1 . 15 . A method for the treatment of an ocular infection of a patient, said method comprising topically administering of an ophthalmic composition comprising an effective amount of ε-polylysine (εPL) to the patient's eye, or a method for the prophylaxis of an ocular infection of a patient, said method comprising topically administering of an ophthalmic composition comprising an effective amount of ε-polylysine (εPL) to the patient's eye before or after the introduction of an inoculum of an ocular pathogen. 16 . The method of claim 15 , wherein the patient is a human or a veterinary patient. 17 . The method of claim 15 , wherein the method is for the treatment of bacterial conjunctivitis. 18 . The method of claim 15 , wherein the method is for the treatment of bacterial keratitis. 19 . The method of claim 15 , wherein the ocular infection is caused by MRSA. 20 . The method of claim 15 , wherein the ophthalmic composition is administered to the patient prior to cataract surgery for prophylaxis against bacterial endophthalmitis. 21 . Use of an ophthalmic composition comprising a pharmaceutically acceptable carrier and an effective amount of ε-polylysine (εPL) for the preparation of a medicament for topical administration to an eye of a patient for the treatment of an ocular infection or for the prophylaxis of an ocular infection when the ophthalmic composition is administered to an eye of a patient before or after the introduction of an inoculum of an ocular pathogen. 22 . The use of claim 21 , wherein the ocular infection is caused by MRSA.

Assignees

Inventors

Classifications

  • A61K38/16Primary

    Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof {(enzyme inhibitors A61K38/005)} · CPC title

  • Antibacterial agents · CPC title

  • A61K9/0048Primary

    Eye, e.g. artificial tears · CPC title

  • Ophthalmic agents · CPC title

  • Ocular inserts or implants · CPC title

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Frequently asked questions

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What does patent US2017196805A1 cover?
An ophthalmic composition for administration to an eye of a patient for the treatment of an ocular infection. The ophthalmic composition contains an ε-polylysine (εPL) in an amount effective to treat or control or prevent the ocular infection.
Who is the assignee on this patent?
Coopervision Int Holding Co Lp
What technology area does this patent fall under?
Primary CPC classification A61K38/16. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Jul 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).