US20200237916A1

US20200237916A1 - Ophthalmic formulation and method for ameliorating presbyopia

Info

Publication number: US20200237916A1
Application number: US16/701,602
Authority: US
Inventors: Luis Felipe Vejarano Restrepo
Original assignee: Individual
Current assignee: Individual
Priority date: 2012-07-19
Filing date: 2019-12-03
Publication date: 2020-07-30
Also published as: MX351230B; CO7250451A2; BR112015001158A2; CN113425715A; HRP20190627T1; TR201905683T4; CN104717981A; PT2874660T; AR092860A1; PL2874660T3; ES2719250T3; US10507245B2; DK2874660T3; WO2014015183A1; US20140024642A1; RU2015102531A; RU2657514C2; MX2015000806A; EP2874660B1; EP2874660A1

Abstract

An ophthalmic formulation having an effective amount of a parasympathomimetic agent comprising pilocarpine, or a pharmaceutically acceptable salt thereof, and one or more α1 adrenergic agonists or antagonists is disclosed. The ophthalmic formulation may enable treatment of conditions adversely affecting the visual acuity of a patient, including presbyopia. A method of using the disclosed ophthalmic formulation to treat or ameliorate symptoms of presbyopia is also disclosed.

Description

INCORPORATION BY REFERENCE TO ANY PRIORITY APPLICATIONS

Any and all applications for which a foreign or domestic priority claim is identified in the Application Data Sheet as filed with the present application are hereby incorporated by reference under 37 CFR 1.57.

BACKGROUND

Field

This application relates to a pharmaceutical preparation comprising a parasympathomimetic drug and an α1 (alpha1) adrenergic agonist or antagonist for ameliorating, reducing or treating presbyopia.

Description of the Related Art

Presbyopia is an age-related reduction in visual acuity due to a decline in near focusing ability, commonly associated with blurred appearance of objects at nearby distances. Symptoms of presbyopia often become noticeable by around age 40 to around age 45. Presbyopia is typically associated with the reduced accommodative ability of the eye. For example, flexibility or elasticity of the crystalline lens and strength of the ciliary muscles often decrease with age. A decrease in the flexibility or elasticity of the crystalline lens or the strength of ciliary muscles can be associated with a decrease in the ability of the eye in adjusting the curvature of the crystalline lens to focus on objects at nearby distances, including objects at around a normal reading distance.
Common treatments of presbyopia include use of eye glasses, such as reading glasses typically worn for near distance vision, and bi-focals or multi-focals to provide both improved near and distance vision for patients who already use correction for distance vision. Corrective contact lenses can also be used to treat presbyopia, including bi-focal, multi-focal or monovision contact lenses. Monovision contact lenses typically include a lens for distance vision in one eye, for example a dominant eye, and a lens for near distance vision in the other eye, for example a non-dominant eye. Surgical options are also available for treating presbyopia, including corrective eye surgery. For example, refractive eye surgery generally involves reshaping of the cornea. Refractive surgery can allow reshaping of the cornea in one eye while leaving the other eye untreated, for example correcting vision only in a non-dominant eye for improved near vision while allowing the dominant eye to maintain distance vision. Implantation of intraocular lenses (IOL) can be another surgical option in treating presbyopia, generally involving replacement of the natural lens with a synthetic one. However, eye glasses or corrective lenses may be cumbersome or provide inadequate treatment, while surgical correction can be invasive and are not without risks. Because these techniques merely compensate for the loss of accommodation by changing the way light enters the eye, patients would have to put on the glasses for near vision and remove the glasses for distance vision, or have only one eye corrected for near vision while the other eye remains uncorrected in order to maintain distance vision. Thus, a way to ameliorate or reduce the symptoms of presbyopia while allowing accommodation is needed.

SUMMARY

In some embodiments, an ophthalmic formulation comprises an effective amount of pilocarpine, or a pharmaceutically acceptable salt thereof, and one or more al adrenergic agonists or antagonists. The one or more α1 adrenergic agonists or antagonists may be selected from a group consisting of phenylephrine, phenylpropanolamine, etylefrine, oxymetazoline, xilometazoline, tramazoline, and a pharmaceutically acceptable salt thereof.
In some embodiments, a method of ameliorating, reducing or treating presbyopia comprises administering an effective amount of an ophthalmic formulation to an eye of a patient. The ophthalmic formulation may include an effective amount of pilocarpine, or a pharmaceutically acceptable salt thereof, and one or more α1 adrenergic agonists or antagonists. The α1 adrenergic agonist may comprise phenylephrine, or a pharmaceutically acceptable salt thereof.

DETAILED DESCRIPTION OF SOME EMBODIMENTS

The embodiments described in this application relate to a pharmaceutical preparation comprising a parasympathomimetic drug and one or more α1 (alpha1) adrenergic agonists or antagonists. In some embodiment, the pharmaceutical preparation described herein is useful for ameliorating, reducing and/or treating presbyopia or symptoms thereof. The pharmaceutical preparation may reduce or eliminate the symptoms of presbyopia while maintaining the accommodative function of the eyes, and allow patients suffering from presbyopia the ability to focus both far and near. In some embodiments, the pharmaceutical preparation can improve near vision of a patient suffering from presbyopia without affecting the distance vision. In some embodiments, the pharmaceutical preparation may be formulated into an ophthalmic formulation that can be applied to the eye of a patient suffering from conditions relating to presbyopia.
As used herein, the terms ameliorate, treat or treatment refer to a reduction in the severity of symptoms of an eye condition adversely affecting visual acuity. In some embodiments, an ophthalmic formulation as described herein is suitable for treating, or reducing the severity of the symptoms of, presbyopia. For example, an ophthalmic formulation as described herein may be suitable for the treatment of presbyopia by enabling the patient to visually focus on objects at a nearby distance, including objects at around a normal reading distance.
As used herein, the terms effective amount include quantities of one or more active ingredients described herein sufficient for the treatment of a condition of the eye adversely affecting visual acuity, including achieving temporary improvement in the symptoms of presbyopia. For example, effective amounts of an active ingredient when applied to one or both eyes of a patient may enable the patient to visually focus on objects at a nearby distance, including objects at a distance around a normal reading distance.
Some embodiments describe a pharmaceutical preparation comprising an effective amount of a parasympathomimetic drug and one or more α1 adrenergic agonist or antagonist. In some embodiments, the pharmaceutical preparation is an ophthalmic formulation. In some embodiments, the ophthalmic formulation comprising an effective amount of a parasympathomimetic drug and one or more α1 adrenergic agonist or antagonist may further comprise one or more of ingredients selected from the group consisting of a vasoconstricting agent, an anti-histamine agent, a non-steroid anti-inflammatory drug, and an lubricant.
In some embodiments, the parasympathomimetic drug is pilocarpine or a pharmaceutically acceptable salt thereof. Pilocarpine is a direct acting parasympathomimetic agent that acts on M₃muscarinic receptor. It can cause the ciliary muscle in the eye to contract and provide near focus. However, it may also cause contraction of the pupil or miosis.
In some embodiments, the one or more α1 adrenergic agonists or antagonists may independently be selected from phenylephrine, phenylpropanolamine, etylefrine, oxymetazoline, xilometazoline, or tramazoline, or a pharmaceutically acceptable salt thereof. In some embodiments, the α1 adrenergic agonists or antagonists may be phenylephrine. Phenylephrine may dilate the pupil, and may reduce pupil contraction due to pilocarpine. In some embodiments, phenylephrine may contribute to the normal movement of pupil in any light situation, and/or reduces miosis. With proper concentrations of pilocarpine and phenylephrine, voluntary accommodation of the eyes can be maintained or restored while the presbyopia symptoms are ameliorated or treated.
In some embodiments of the ophthalmic formulation, pilocarpine or a pharmaceutically acceptable salt thereof, may be present in the amount of from about 0.1% to about 2.0%, from about 0.1% to about 1.9%, from about 0.2% to about 1.9%, including from about 0.3% to about 1.9%, from about 0.4% to about 1.9%, from about 0.2% to about 1.8%, from about 0.3% to about 1.7%, from about 0.1% to about 1.8%, from about 0.1% to about 1.5%, from about 0.1% to about 1.3%, from about 0.1% to about 1.2% from about 0.1% to about 0.9%, from about 0.1% to about 0.7%, from about 0.4% to about 1.6%, from about 0.5% to about 1.3%, or at about 0.4%, about 0.5%, about 0.6%, about 0.7%, about 0.8%, about 0.9%, about 1.0%, about 1.1%, about 1.2%, by weight.
In some embodiments of the ophthalmic formulation, the phenylephrine or a pharmaceutically acceptable salt thereof, may be present in the amount of from about 0.1% to about 7%, from about 0.1% to about 6%, from about 0.1% to about 5.5%, from about 0.1% to about 4.5%, from about 0.1% to about 3%, from about 0.2% to about 3.5%, from about 0.2% to about 4.5%, from about 0.2% to about 5.5%, from about 0.2% to about 6%, from about 0.3% to about 5%, from about 0.4% to about 4%, from about 0.5% to about 3%, from about 0.6% to about 3%, from about 0.6% to about 2.5%, from about 0.7% to about 2.5%, from about 0.7% to about 2.0%, or about 0.5%, about 1%, about 1.5%, about 2%, about 2.5%, about 3, about 3.5%, about 4%, about 5% by weight.
In some embodiments, an ophthalmic formulation may further comprise a vasoconstricting agent. In some embodiments, a suitable vasoconstricting agent or drug comprises naphazoline, or a pharmaceutically acceptable salt thereof. An ophthalmic formulation suitable for the treating a condition of the eye adversely affecting the visual acuity of a patient, for example presbyopia, may comprise effective amounts of one or more vasoconstricting agents. Alternatively, an ophthalmic formulation may not comprise e a vasoconstricting agent.
For example, an ophthalmic formulation may include by weight from about 0.001% to about 0.020%, including from about 0.002% to about 0.018%, including from about 0.004% to about 0.016%, including from about 0.006% to about 0.01%2, including from about 0.001% to about 0.015%, including from about 0.001% to about 0.012%, including from about 0.001% to about 0.011%, including from about 0.001% to about 0.010%, including from about 0.001% to about 0.009%, including from about 0.001% to about 0.008%, including from about 0.002% to about 0.008%, including from about 0.003% to about 0.009%, including about 0.002%, about 0.003%, about 0.004%, about 0.005%, about 0.006%, about 0.007%, about 0.008%, about 0.009%, about 0.010%, or about 0.012%, of naphazoline, or a pharmaceutically acceptable salt thereof.
In some embodiments, an ophthalmic formulation also optionally comprises one or more anti-histamine agents. A suitable anti-histamine agent or drug may be independently selected from pheniramine, chlorpheniramine, dexchlorpheniramine, dexbrompheniramine, deschlorpheniramine, triprolidine, brompheniramine, iodopheniramine, fluorpheniramine, or a pharmaceutically acceptable salt thereof. In some embodiments, the anti-histamine agent is pheniramine, or a pharmaceutically acceptable salt thereof. Pheniramine may serve to avoid conjunctival injection or congestion and reduce red eye. It also has a minimal effect on the ciliary muscle, and may improve accommodation. Pheniramine or a pharmaceutically acceptable salt thereof, may be present in an amount of from about 0.01% to about 0.20%, from about 0.05% to about 0.15%, from about 0.02% to about 0.10%, from about 0.03% to about 0.09%, from about 0.04% to about 0.08%, from about 0.02% to about 0.20%, from about 0.04% to about 0.15%, from about 0.04% to about 0.15%, at about 0.01%, about 0.02%, about 0.03%, about 0.04%, about 0.05%, about 0.06%, about 0.07%, about 0.08%, about 0.09%, or about 0.10% by weight in the ophthalmic formulation. Alternatively, an ophthalmic formulation may not comprise an anti-histamine agent.
In some embodiments, an ophthalmic formulation may further comprise a non-steroid anti-inflammatory drugs (NSAID). The NSAID may reduce or eliminate anterior segment inflammation. In some embodiments, a suitable NSAID is independently selected from the group consisting of nepafenac, meloxicam, diclofenac, bendazac, ketorolac, oxyphenbutazone, bromfenac, flurbiprofen, pranoprofen, surprofen, or indomethacin, and a pharmaceutically acceptable salt thereof. In some embodiments, an ophthalmic formulation comprises at least one of nepafenac or meloxicam. Alternatively, an ophthalmic formulation may not comprise a non-steroid anti-inflammatory drug.
In some embodiments, an ophthalmic formulation may be formulated to further comprise an effective amount of a NSAID nepafenac. For example, an ophthalmic formulation formulated to comprise nepafenac may include by weight from about 0.01% to about 0.10%, including from about 0.02% to about 0.09%, including from about 0.03% to about 0.08%, including from about 0.04% to about 0.07%, including from about 0.01% to about 0.09%, including from about 0.01% to about 0.08%, including from about 0.01% to about 0.07%, including from about 0.01% to about 0.06%, including from about 0.01% to about 0.05%, including from about 0.01% to about 0.04%, including from about 0.01% to about 0.03%, including from about 0.02% to about 0.08%, including from about 0.02% to about 0.07%, including from about 0.02% to about 0.06%, including from about 0.02% to about 0.05%, including about 0.02%, about 0.04%, about 0.03%, about 0.04%, or about 0.05% of nepafenac, or a pharmaceutically acceptable salt thereof.
Alternatively, the NSAID may be meloxicam. For example, the ophthalmic formulation may include by weight from about 0.001% to about 0.015%, including from about 0.001% to about 0.014%, including from about 0.001% to about 0.013, including from about 0.001% to about 0.014%, including from about 0.001% to about 0.014%, including from about 0.001% to about 0.012%, including from about 0.01% to about 0.009%, including from about 0.001% to about 0.008%, including from about 0.002% to about 0.007%, including from about 0.002% to about 0.006%, including from about 0.003% to about 0.012%, including from about 0.003% to about 0.01%, including from about 0.003% to about 0.009%, including from about 0.004% to about 0.012%, including about 0.003%, about 0.004%, about 0.005%, about 0.006%, about 0.007%, about 0.008%, about 0.009%, about 0.010%, or about 0.011% of meloxicam, or a pharmaceutically acceptable salt thereof.
An ophthalmic formulation, as described herein, may also further comprise a lubricant or lubricating agent. In some embodiments, the lubricant or lubricating agent may facilitate administration of the ophthalmic formulation. Suitable lubricants can be independently selected from polyethyleneglycol 400 or propyleneglycol. In some embodiments, the ophthalmic formulation comprises one or more suitable lubricants or lubricating agents. Alternatively, an ophthalmic formulation may not comprise a lubricant or lubricating agent.
In some embodiments, where polyethyleneglycol 400 is selected as the lubricant for the ophthalmic formulation, the ophthalmic formulation may comprise by weight of from about 0.01% to about 0.30%, including from about 0.02% to about 0.25%, 0.03% to about 0.20%, 0.04% to about 0.15%, 0.05% to about 0.15%, 0.05% to about 0.10%, 0.10% to about 0.30%, 0.10% to about 0.20%, 0.06% to about 0.20%, 0.05% to about 0.20%, including about 0.05%, about 0.10%, or about 0.15% of polyethyleneglycol 400 or a pharmaceutically acceptable salt thereof.
In some embodiments, the lubricant may be propyleneglycol. For example, an ophthalmic formulation may include by weight of from about 0.01% to about 0.20%, including from about 0.02% to about 0.10%, including from about 0.04% to about 0.09%, including from about 0.04% to about 0.08%, including from about 0.04% to about 0.06%, including from about 0.02% to about 0.10%, including from about 0.02% to about 0.12%, including from about 0.02% to about 0.14%, including from about 0.05% to about 0.20%, including from about 0.05% to about 0.15%, including about 0.01%, about 0.02%, about 0.03%, about 0.04%, about 0.05%, about 0.06%, about 0.07%, about 0.08%, about 0.09%, or about 0.10% of propyleneglycol or a pharmaceutically acceptable salt thereof.
In some embodiments, the ophthalmic formulation comprises one or more components to facilitate application of the ophthalmic formulation. For example, the ophthalmic formulation may also optionally comprise a pharmaceutically acceptable carrier, antibacterial agent, or a preservative. In some embodiments, a pharmaceutically acceptable carrier comprises purified water.
Some embodiments described herein relate to a method of treating a condition of the eye adversely affecting near distance visual acuity of a patient, including ameliorating symptoms of presbyopia. A method of treating the symptoms of presbyopia may include applying to one or both eyes of a patient an ophthalmic formulation as described herein. The ophthalmic formulation may be applied to the eye of a patient as a liquid, a gel, a solution, a suspension, or any combination thereof. In some embodiments, the ophthalmic formulation is administered to the eye via an ocular route, including topical application to the conjunctiva.
An ophthalmic formulation may comprise one or more components, each component may be administered sequentially or simultaneously to the one or both eyes of a patient for improved visual acuity, including for the treatment of the symptoms of presbyopia. For example, application of an ophthalmic formulation comprising an effective amount of a parasympathomimetic agent and an effective amount of an α1 adrenergic agonist or antagonist may ameliorate symptoms of presbyopia while allowing voluntary accommodation.
In some embodiments, an ophthalmic formulation as described herein is applied to one or both eyes of a patient showing symptoms of presbyopia to improve the ability of the patient to focus on objects at a nearby distance, including objects at around a normal reading distance. In some embodiments, application of an ophthalmic formulation as described herein may sufficiently improve the near distance visual acuity of a patient independent of other methods of treatment. For example, administration of an ophthalmic formulation as described herein may enable a patient to focus on objects at a distance around a normal reading distance without use of corrective lenses or corrective eye surgery. Administration of the ophthalmic formulation may relieve symptoms for a patient in the early stages of presbyopia, including enabling near distance visual acuity without use of corrective lenses or glasses.
In some embodiments, an ophthalmic formulation as described herein is administered to a patient having symptoms of presbyopia, in addition to symptoms from myopia or hyperopia to facilitate near distance visual acuity such that the patient may not need to depend on the corrective treatment such as bifocals/multi-focals lenses or monovision contact lenses or to remove the glasses to read in myopes.
In some embodiments, an ophthalmic formulation as described herein is administered to one or both eyes of a patient to provide treatment for presbyopia as an alternative to corrective eye surgery. For example, an ophthalmic formulation as described herein may be administered to a patient having symptoms of presbyopia where the patient either prefers not to or cannot receive corrective eye surgery to treat presbyopia. The ophthalmic formulation as described herein may also be administered to a myopic or hyperopic patient (with or without astigmatism) having symptoms of presbyopia, but prefers to receive treatment only for the far vision defect. Alternatively, an ophthalmic formulation as described herein may be administered to a patient who continues to have symptoms of presbyopia after the patient has undergone corrective eye surgery for presbyopia. The ophthalmic formulation may be used in conjunction with corrective eye surgery for presbyopia to further reduce the symptoms of presbyopia. In some embodiments, the ophthalmic formulation as described herein is applied to one or both eyes of a patient to reduce a decline in near distance visual acuity after undergoing a corrective eye surgery for far vision at a younger age.
In some embodiments, administration of an ophthalmic formulation as described herein facilitates improvement in the symptoms of presbyopia for a patient who has reversed a previously received corrective eye surgery for presbyopia. For example, administration of the ophthalmic formulation may enable reestablishment of binocularity for a patient after a reversal or regression of a previously received monovision laser surgery for treating presbyopia.
In some embodiments, an ophthalmic formulation as described herein is administered to a patient to improve the ability of the patient to focus on nearby objects after the patient has undergone corrective surgery for treatment of ocular conditions other than presbyopia, including for example a corrective eye surgery for the treatment of a cataract.
In some embodiments, an ophthalmic formulation as described herein is used in conjunction with other treatments for eye conditions, including treatments for the symptoms of presbyopia. For example, an ophthalmic formulation as described herein may be administered to a patient in conjunction with use of mono-focal intraocular lenses, multi-focal intraocular lenses, or accommodative intraocular lenses to improve the near focusing ability of the patient.
In some embodiments, application of an ophthalmic formulation as described herein is suitable for reducing the symptoms of ocular hypertension. The ophthalmic formulation may be administered to an eye of a patient to improve symptoms of ocular hypertension through a reduction in intraocular pressure.
Although this invention has been disclosed in the context of certain embodiments and examples, it will be understood by those skilled in the art that the invention extends beyond the specifically disclosed embodiments to other alternative embodiments and/or uses of the invention and obvious modifications and equivalents thereof. In addition, while several variations of the embodiments of the invention have been shown and described in detail, other modifications, which are within the scope of this invention, will be readily apparent to those of skill in the art based upon this disclosure. It is also contemplated that various combinations or sub-combinations of the specific features and aspects of the embodiments may be made and still fall within the scope of the invention. It should be understood that various features and aspects of the disclosed embodiments can be combined with, or substituted for, one another in order to form varying modes of the embodiments of the disclosed invention. Thus, it is intended that the scope of the invention herein disclosed should not be limited by the particular embodiments described above.

Claims

1.-20. (canceled)

21. An ophthalmic formulation comprising an effective amount of about 0.1% to about 0.9% by weight pilocarpine or a pharmaceutically acceptable salt thereof, and about 0.3% to about 3% by weight phenylephrine or a pharmaceutically acceptable salt thereof.

22. The ophthalmic formulation of claim 21, wherein the ophthalmic formulation comprises about 0.2% to about 0.7% by weight pilocarpine or a pharmaceutically acceptable salt thereof.

23. The ophthalmic formulation of claim 21, wherein the ophthalmic formulation comprises about 0.6% to about 0.7% by weight phenylephrine or a pharmaceutically acceptable salt thereof.

24. The ophthalmic formulation of claim 21, further comprising about 0.001% to about 0.020% by weight naphazoline or a pharmaceutically acceptable salt thereof.

25. The ophthalmic formulation of claim 24, wherein the formulation comprises about 0.003% naphazoline or a pharmaceutically acceptable salt thereof.

26. The ophthalmic formulation of claim 21, further comprising an anti-histamine selected from the group consisting of pheniramine, chlorpheniramine, dexchlorpheniramine, dexbrompheniramine, deschlorpheniramine, triprolidine, brompheniramine, iodopheniramine, fluorpheniramine, and a pharmaceutically acceptable salt thereof.

27. The ophthalmic formulation of claim 26, wherein the anti-histamine is pheniramine or a pharmaceutically acceptable salt thereof.

28. The ophthalmic formulation of claim 27, wherein the pheniramine is present in an amount of about 0.02% to about 0.2% by weight.

29. The ophthalmic formulation of claim 21, further comprises a non-steroidal anti-inflammatory drug.

30. The ophthalmic formulation of claim 29, wherein the non-steroidal anti-inflammatory drug is selected from the group consisting of nepafenac, meloxicam, diclofenac, bendazac, ketorolac, oxyphenbutazone, bromfenac, flurbiprofen, pranoprofen, surprofen, indomethacin, and a pharmaceutically acceptable salt thereof.

31. The ophthalmic formulation of claim 29, wherein the non-steroidal anti-inflammatory drug is selected from the group consisting of nepafenac, bromfenac, ketorolac and meloxicam.

32. The ophthalmic formulation of claim 29, wherein the non-steroidal anti-inflammatory drug is ketorolac.

33. A method of ameliorating, reducing or treating presbyopia comprising administering an effective amount of an ophthalmic formulation of claim 21 to an eye of a patient.

34. The method of claim 33, wherein the ophthalmic formulation further comprises an anti-histamine selected from the group consisting of pheniramine, chlorpheniramine, dexchlorpheniramine, dexbrompheniramine, deschlorpheniramine, triprolidine, brompheniramine, iodopheniramine, fluorpheniramine, and a pharmaceutically acceptable salt thereof.

35. The method of claim 34, wherein the ophthalmic formulation further comprises a non-steroidal anti-inflammatory drug selected from the group consisting of nepafenac, meloxicam, diclofenac, bendazac, ketorolac, oxyphenbutazone, bromfenac, flurbiprofen, pranoprofen, surprofen, indomethacin, and a pharmaceutically acceptable salt thereof.