US20120225918A1 - Compositions and Methods for Non-Surgical Treatment of Ptosis - Google Patents

Compositions and Methods for Non-Surgical Treatment of Ptosis Download PDF

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Publication number
US20120225918A1
US20120225918A1 US13/218,584 US201113218584A US2012225918A1 US 20120225918 A1 US20120225918 A1 US 20120225918A1 US 201113218584 A US201113218584 A US 201113218584A US 2012225918 A1 US2012225918 A1 US 2012225918A1
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oxymetazoline
eye
phenylephrine
weight percent
ptosis
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English (en)
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Mark Silverberg
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VOOM LLC
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VOOM LLC
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Priority to US13/218,584 priority Critical patent/US20120225918A1/en
Assigned to VOOM, LLC reassignment VOOM, LLC ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: SILVERBERG, MARK
Priority to US13/270,577 priority patent/US8357714B2/en
Priority to MX2013009597A priority patent/MX345042B/es
Priority to SI201231705T priority patent/SI2680829T1/sl
Priority to PT127094217T priority patent/PT2680829T/pt
Priority to LTEP12709421.7T priority patent/LT2680829T/lt
Priority to RU2013142602/15A priority patent/RU2582392C2/ru
Priority to ES12709421T priority patent/ES2750123T3/es
Priority to BR112013022094A priority patent/BR112013022094A2/pt
Priority to CA2827285A priority patent/CA2827285C/en
Priority to EP12709421.7A priority patent/EP2680829B1/en
Priority to AU2012223615A priority patent/AU2012223615B2/en
Priority to PCT/US2012/026496 priority patent/WO2012118704A1/en
Priority to EP19199263.5A priority patent/EP3653205A3/en
Priority to RS20191580A priority patent/RS59636B1/sr
Priority to NZ614719A priority patent/NZ614719B2/en
Priority to DK12709421T priority patent/DK2680829T3/da
Priority to CN201280011433.6A priority patent/CN103501771B/zh
Priority to SG2013062245A priority patent/SG192801A1/en
Priority to KR1020137026050A priority patent/KR101889392B1/ko
Priority to JP2013556744A priority patent/JP6106100B2/ja
Priority to HUE12709421A priority patent/HUE046740T2/hu
Priority to PL12709421T priority patent/PL2680829T3/pl
Priority to US13/408,364 priority patent/US9018240B2/en
Publication of US20120225918A1 publication Critical patent/US20120225918A1/en
Priority to ZA2013/07262A priority patent/ZA201307262B/en
Priority to US14/625,099 priority patent/US9867808B2/en
Priority to US15/837,325 priority patent/US20180338953A1/en
Priority to US16/577,262 priority patent/US10912765B2/en
Priority to CY20191101170T priority patent/CY1122565T1/el
Priority to HRP20192266TT priority patent/HRP20192266T1/hr
Priority to US16/892,645 priority patent/US20200360345A1/en
Priority to US17/679,278 priority patent/US20220218669A1/en
Abandoned legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/13—Amines
    • A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/13—Amines
    • A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
    • A61K31/137—Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine or methadone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4174—Arylalkylimidazoles, e.g. oxymetazolin, naphazoline, miconazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0048—Eye, e.g. artificial tears
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D47/00—Closures with filling and discharging, or with discharging, devices
    • B65D47/04—Closures with discharging devices other than pumps
    • B65D47/06—Closures with discharging devices other than pumps with pouring spouts or tubes; with discharge nozzles or passages
    • B65D47/18—Closures with discharging devices other than pumps with pouring spouts or tubes; with discharge nozzles or passages for discharging drops; Droppers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis

Definitions

  • Ptosis is abnormal partial or complete drooping of the upper eyelid. Ptosis occurs when the muscles that raise the eyelid (levator palpebrae superioris and Müller's muscles) are not strong enough to do so properly. It can affect one eye or both eyes and is more common in the elderly, as muscles in the eyelids may begin to deteriorate. Fatigue is a common reversible cause of ptosis, giving an affected individual an appearance characterized by “tired eyes.”
  • Non-surgical modalities for the treatment of ptosis include the use of “crutch” glasses or special scleral contact lenses to support the eyelid.
  • compositions and methods useful in the treatment of ptosis include an effective amount of a long-acting alpha adrenergic agonist and, optionally, a short-acting alpha adrenergic agonist.
  • the compositions are formulated for topical administration to the eye.
  • the compositions and methods of the invention can be used to treat ptosis in a non-surgical method. The methods provide long-lasting reversible treatment for ptosis in suitable subjects.
  • oxymetazoline unexpectedly can be administered to an eye to treat ptosis without affecting pupil size. This observation was unexpected because oxymetazoline is an alpha adrenergic agonist, and other alpha adrenergic agonists are known commonly to cause pupillary dilation (mydriasis).
  • compositions and methods of the invention are disclosed to be useful to treat ptosis without causing mydriasis commonly obtained with alpha adrenergic agonists topically administered to the eye.
  • oxymetazoline and phenylephrine unexpectedly can be used in combination to treat ptosis, with a synergistic effect. More particularly, it has been discovered that the effect on lid aperture of a combination of oxymetazoline and phenylephrine is greater than the sum of the effects of oxymetazoline alone and phenylephrine alone. Moreover, such combination can also be used to treat ptosis without causing clinically significant mydriasis.
  • compositions and methods of the invention are disclosed to be useful to treat visual field defects arising from ptosis.
  • An aspect of the invention is a method for treating ptosis in a subject.
  • the method includes the step of administering an effective amount of oxymetazoline to the exterior surface of an eye of a subject in need of such treatment.
  • the administering results in at least a 1 millimeter (mm) increase in the vertical separation of the upper and lower lids of the eye. In one embodiment the administering results in at least a 10 percent increase in the vertical separation of the upper and lower lids of the eye.
  • the oxymetazoline is formulated as a pharmaceutical composition comprising at least 0.05 weight percent oxymetazoline in an ophthalmologically acceptable carrier. In one embodiment the oxymetazoline is provided as a pharmaceutically acceptable salt of oxymetazoline.
  • the administering is administering as a single drop.
  • administering is administering at least once daily. In one embodiment the administering is administering once daily.
  • the subject does not have an allergic ocular condition calling for treatment of the eye with oxymetazoline. In one embodiment the subject does not have eyelid swelling. In one embodiment the subject has not undergone refractive eye surgery.
  • An aspect of the invention is a method for treating ptosis in a subject.
  • the method includes the step of administering an effective amount of a long-acting alpha adrenergic agonist and an effective amount of a short-acting alpha adrenergic agonist to the exterior surface of an eye of a subject in need of such treatment.
  • the long-acting alpha adrenergic agonist is oxymetazoline or a pharmaceutically acceptable salt thereof.
  • the short-acting alpha adrenergic agonist is phenylephrine or a pharmaceutically acceptable salt thereof.
  • the administering results in at least a 1 millimeter (mm) increase in the vertical separation of the upper and lower lids of the eye. In one embodiment the administering results in at least a 10 percent increase in the vertical separation of the upper and lower lids of the eye.
  • the oxymetazoline is formulated as a pharmaceutical composition comprising at least 0.05 weight percent oxymetazoline in art ophthalmologically acceptable carrier.
  • the long-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising at least 0.1 weight percent oxymetazoline and the short-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising at least 0.15 weight percent phenylephrine. In one embodiment the long-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising at least 0.1 weight percent oxymetazoline and the short-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising at least 0.25 weight percent phenylephrine.
  • the long-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising 0.1 weight percent oxymetazoline and the short-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising 0.25 weight percent phenylephrine.
  • the oxymetazoline is formulated together with phenylephrine as a pharmaceutical composition comprising at least 0.1 weight percent oxymetazoline and at least 0.15 weight percent phenylephrine in an ophthalmologically acceptable carrier. In one embodiment the oxymetazoline is formulated together with the phenylephrine as a pharmaceutical composition comprising at least 0.1 weight percent oxymetazoline and at least 0.25 weight percent phenylephrine in an ophthalmologically acceptable carrier. In one embodiment the oxymetazoline is formulated together with the phenylephrine as a pharmaceutical composition comprising 0.1 weight percent oxymetazoline and 0.25 weight percent phenylephrine in an ophthalmologically acceptable carrier.
  • the administering is administering as a single drop.
  • administering is administering at least once daily. In one embodiment the administering is administering once daily.
  • the subject does not have an allergic ocular condition calling for treatment of the eye with oxymetazoline. In one embodiment the subject does not have eyelid swelling. In one embodiment the subject has not undergone refractive eye surgery.
  • An aspect of the invention is a pharmaceutical composition, comprising oxymetazoline, a short-acting alpha adrenergic agonist, and a pharmaceutically acceptable carrier, formulated for topical ophthalmic use.
  • the short-acting alpha adrenergic agonist is phenylephrine.
  • the oxymetazoline is present at a concentration of at least 0.1 weight percent.
  • the phenylephrine is present at a concentration of 0.15 to 1.5 weight percent.
  • the oxymetazoline is present at a concentration of at least 0.1 weight percent and the phenylephrine is present at a concentration of at least 0.25 weight percent.
  • the oxymetazoline is present at a concentration of 0.1 weight percent and the phenylephrine is present at a concentration of 0.25 weight percent.
  • composition further comprises an antioxidant.
  • composition further comprises vitamin A.
  • composition further comprises an astringent.
  • composition further comprises a lubricant.
  • composition further comprises a blue dye.
  • FIG. 1 is a series of three photographic images of the face of a subject before (top), 30 minutes after (middle), and 90 minutes after (bottom) topical administration of a single drop of oxymetazoline 0.1% to each eye.
  • FIG. 2 is a series of three photographic images of the face of a subject before (top), and 25 minutes (middle) and three and one-half hours (bottom) following topical administration of a single drop of oxymetazoline 0.1% to the subject's left eye.
  • FIG. 3A is a baseline visual field map of a ptotic eye in a patient with significant ptosis of one eye. Open ovals represent seen spots. Closed ovals represent not seen spots.
  • FIG. 3B is a visual field map of the same ptotic eye as in FIG. 3A , measured 2 hours and 20 minutes following administration of a single drop of 0.1% oxymetazoline to that eye.
  • FIG. 3C is a visual field map of the same ptotic eye as in FIG. 3A and FIG. 3B , measured 4 hours following administration of a single drop of 0.1% oxymetazoline to that eye.
  • the upper eyelids are normally lifted by contraction of the levator palpebrae superioris (levator) and Müller's (Mueller's) muscles.
  • levator palpebrae superioris
  • Müller's Müller's
  • Ptosis creates a tired-looking appearance that can be cosmetically undesired; in more severe instances ptosis can interfere with vision in the affected eye(s).
  • ptosis may also be due to a myogenic, neurogenic, aponeurotic, mechanical, or traumatic cause; it usually occurs isolated, but it may be associated with various other conditions, like hereditary, immunological, or degenerative disorders, tumors, and infections.
  • Myogenic causes of ptosis can include diseases which may cause weakness in muscles or nerve damage, such as myasthenia gravis and chronic progressive external ophthalmoplegia. Dystrophy or dysgenesis of the levator and/or Müller's muscles are the most common causes of congenital ptosis.
  • Ptosis may be caused by damage to the third cranial nerve (oculomotor nerve) which controls the muscles which raise the upper eyelid.
  • Congenital neurogenic ptosis is believed to be caused by Horner syndrome (also known as Horner's syndrome), in which a mild ptosis due to the paresis of the Müller muscle may be associated with ipsilateral miosis (pupillary constriction) and anhidrosis.
  • Acquired Horner syndrome may result after trauma, neoplastic insult, or even vascular disease.
  • Acquired ptosis is commonly caused by aponeurotic ptosis. This can occur as a result of senescence, dehiscence or disinsertion of the levator aponeurosis. Moreover, chronic inflammation or intraocular surgery can lead to the same effect.
  • Ptosis due to trauma can ensue after an eyelid laceration with transection of the upper eyelid elevator muscles or disruption of the neural input.
  • ptosis causes of ptosis include eyelid neoplasms, neurofibromas, or the cicatrization after inflammation or surgery. Mild ptosis may occur with aging.
  • compositions and methods of the invention may be particularly useful for treating ptosis in subjects with functional, or at least partially functional, levator and/or Müller's muscles and their respective aponeuroses.
  • the present inventor has surprisingly found, through a process of evaluating a number of agents over a range of concentrations of such agents, that certain alpha adrenergic agonists, including in particular oxymetazoline 0.1 percent, provide highly effective treatment of ptosis, lasting for several hours, following topical administration of just a single drop of such agent to an affected eye.
  • An aspect of the invention is a method for treating ptosis in a subject.
  • the method includes the step of administering an effective amount of oxymetazoline to the exterior surface of an eye of a subject in need of such treatment.
  • “treating” means reducing, even if only temporarily, the severity of a condition or disease in a subject having such condition or disease. In one embodiment the reducing is eliminating, even if only temporarily.
  • ptosis in a subject is said to be treated in accordance with the method if the ptosis is reduced or eliminated, even if only temporarily.
  • a “subject” refers to a living mammal. In one embodiment the subject is a human.
  • a “subject in need of such treatment” is a subject having a condition in need of treatment.
  • a subject in need of such treatment is a subject that has ptosis of at least one eyelid.
  • a subject has ptosis when at least the left or the right upper eyelid is subjectively or objectively ptotic compared to historical control and/or the other eye.
  • both the left and the right upper eyelid are ptotic, although not necessarily to the same degree.
  • Historical control can be provided in the form of a photographic image, for example.
  • a subject is said to have ptosis when at least the left or the right upper eyelid is ptotic by at least one millimeter (mm) compared to historical control and/or the other eye.
  • mm millimeter
  • Such measurement involves measuring the widest separation of the upper and lower lids in the sagittal plane, typically but not necessarily across the center of the pupil, with the subject at rest, i.e., without any conscious effort on the part of the subject to widen the lids.
  • the measurement is made on the eye or eyes of a living subject.
  • the measurement is made or based on a photographic image of the subject's eye or eyes.
  • Oxymetazoline is 3-(4,5-dihydro-1H-imidazol-2-ylmethyl)-2,4-dimethyl-6-tert-butyl-phenol, CAS number 1491-59-4. It was developed from xylometazoline at E. Merck Darmstadt by Fruhstorfer in 1961 (German Patent 1,117,588).
  • Oxymetazoline is a well known potent alpha adrenergic agonist that finds use as a vasoconstrictor. It has been used in the form of its hydrochloride salt as the principal active agent in topical nasal decongestants such as Afrin (Schering Plough). Afrin provides 12-hour relief for sinus congestion and was first sold as a prescription medication in 1966. It has been available as an over-the-counter drug since 1975.
  • Oxymetazoline has also been used to treat eye redness due to minor irritation (marketed in the form of eye drops as Visine® L.R.® (Johnson & Johnson) and Ocuclear® (Schering)). Each of these eye drop formulations contains 0.025 percent oxymetazoline hydrochloride (HCl) as the active agent.
  • Indications for Visine® L.R.®, and Ocuclear® are redness due to minor eye irritation, and burning, irritation, and dryness of the eye caused by wind, sun, and other minor irritants.
  • Ocuclear is also marketed for use in the treatment of acute allergic conjunctivitis and non-infectious conjunctivitis.
  • U.S. Pat. No. 6,730,691 to Galin discloses the topical application of ophthalmic solutions containing one or more alpha adrenergic blocking agents to inhibit undesirable visual anomalies, such as photophobia, glare, secondary images, and haloing, in individuals who have undergone refractive eye surgery.
  • the solution includes an anti-irritant agent selected from the group consisting of naphthazoline, oxymetazoline, and tetrahydrozaline.
  • such anti-irritant is disclosed to be included in a concentration of from about 0.025 percent by weight to about 0.1 percent by weight.
  • U.S. Pat. No. 7,022,740 to Mackles discloses lubricious ophthalmic solutions consisting essentially of an aqueous solution of a monographed polyol (e.g., polyvinyl alcohol), borate, a monographed polysorbate (e.g., monolaurate, monopalmitate, monostearate), preservative, and buffer.
  • a monographed polyol e.g., polyvinyl alcohol
  • borate e.g., a monographed polysorbate
  • preservative e.g., monolaurate, monopalmitate, monostearate
  • pharmacologically active substances soluble within such solution can be formulated together with the solution, including ophthalmic vasoconstrictors such as ephedrine HCl, naphazoline HCl, phenylephrine EHCl, tetrahydrozoline HCl, and oxymetazoline HCl, the latter at 0.05 percent.
  • ophthalmic vasoconstrictors such as ephedrine HCl, naphazoline HCl, phenylephrine EHCl, tetrahydrozoline HCl, and oxymetazoline HCl
  • compositions and methods for the treatment and prevention of eyelid swelling are based on osmotically active agent and/or a vasoconstrictor and/or an astringent.
  • the composition is disclosed to include a vasoconstrictor, including nephazoline, oxymetazoline, phenylephrine, or tetrahydrozine. Eyelid swelling was measured using 3D scanning technology.
  • an effective amount of oxymetazoline is administered to the exterior surface of an eye.
  • an “effective amount” is an amount that is sufficient to achieve a desired biological result.
  • an effective amount of oxymetazoline is an amount of oxymetazoline that is sufficient to treat ptosis in a subject having ptosis.
  • the effective amount can vary depending on such factors as the disease or condition being treated, or the severity of the disease or condition. One of skill in the art may empirically determine an effective amount of a particular agent without necessitating undue experimentation.
  • the effective amount is administered to the eye or eyes intended for treatment.
  • the effective amount of oxymetazoline is administered to the left eye.
  • Administering can be accomplished using any suitable method for topical administration of a pharmaceutical agent to the exterior surface of an eye.
  • the administering involves delivering the agent in dropwise fashion to the eye.
  • One or more drops can be administered to the eye.
  • a single drop is administered to the eye.
  • the exterior surface of an eye refers to any portion of the surface of an eye that is normally visible and/or accessible within the palpebral fissure, e.g., the surface of the eye that is normally exposed and/or accessible between the upper and lower eyelids.
  • This surface can include any or all of the following structures: the cornea, the conjunctiva, and the tear sac. In one embodiment this surface is accessible without manual manipulation of the upper or lower eyelids to permit administration. In one embodiment this surface is made accessible by manually opening or widening the palpebral fissure to permit or assist in administration.
  • the method results in at least a 0.5 mm increase in the vertical separation of the upper and lower lids of the eye.
  • the increase is the difference between the separation of the lids before treatment and separation following treatment.
  • the vertical separation can be measured using any suitable method.
  • measuring involves measuring the widest separation of the upper and lower lids in the sagittal plane, typically but not necessarily across the center of the pupil, with the subject at rest, i.e., without any conscious effort on the part of the subject to widen the lids.
  • the measurement may be aided by asking the subject to look at a distant fixation light or point.
  • the measurement is made on the eye or eyes of a living subject, for example using a fine point metric ruler.
  • the measurement is made or based on a photographic image of the subject's eye or eyes, for example using a fine point metric ruler or a magnifier with a metric graticule (Edmund Scentific, Paramus, N.J.).
  • the method results in at least a 1 mm increase in the vertical separation of the upper and lower lids of the eye.
  • the increase is the difference between the separation of the lids before treatment and the separation of the lids following treatment. For example, if the separation is 8 mm before treatment and the separation is 10 mm following treatment, the increase is 2 mm. Since there may be some time lag in reaching the maximum effect, in one embodiment the increase is the maximum increase achieved following administration of the active agent. For example, if the separation is 8 mm before treatment, 9 mm immediately after treatment, 10 mm 30 minutes after treatment, and 8 mm 16 hours after treatment, the increase is 2 mm.
  • the method results in at least a 5 percent increase in the vertical separation of the upper and lower lids of the eye.
  • the method results in at least a 10 percent increase in the vertical separation of the upper and lower lids of the eye. In one embodiment the method results in at least a 20 percent increase in the vertical separation of the upper and lower lids of the eye.
  • the oxymetazoline is formulated as a pharmaceutical composition comprising at least 0.05 weight percent oxymetazoline in an ophthalmologically acceptable carrier. In one embodiment the oxymetazoline is formulated as a pharmaceutical composition comprising at least 0.1 weight percent oxymetazoline in an ophthalmologically acceptable carrier.
  • the invention further embraces embodiments in which a higher weight percentage of oxymetazoline is used, for example, up to and including 1.0 weight percent oxymetazoline. Accordingly, in various embodiments the oxymetazoline may be present at a concentration of 0.05, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, or 1.0 weight percent, or any concentration therebetween. In one embodiment the oxymetazoline is present at a concentration of 0.1 weight percent.
  • an “ophthalmologically acceptable carrier” is any pharmaceutically acceptable carrier that is suitable for topical administration to the eye.
  • the oxymetazoline is provided as a pharmaceutically acceptable salt of oxymetazoline.
  • pharmaceutically acceptable salts is art-recognized, and refers to relatively non-toxic, inorganic and organic acid addition salts of compositions of the present invention or any components thereof, including without limitation, therapeutic agents, excipients, other materials and the like.
  • pharmaceutically acceptable salts include those derived from mineral acids, such as hydrochloric acid and sulfuric acid, and those derived from organic acids, such as ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, and the like.
  • suitable inorganic bases for the formation of salts include but are not limited to the hydroxides, carbonates, and bicarbonates of ammonia, sodium, lithium, potassium, calcium, magnesium, aluminum, zinc and the like. Salts may also be formed with suitable organic bases, including those that are non-toxic and strong enough to form such salts.
  • the class of such organic bases may include mono-, di-, and trialkylamines, such as methylamine, dimethylamine, and triethylamine; mono-, di- or trihydroxyalkylamines such as mono-, di-, and triethanolamine; amino acids, such as arginine and lysine; guanidine; N-methylglucosamine; N-methylglucamine; L-glutamine; N-methylpiperazine; morpholine; ethylenediamine; N-benzylphenethylamine; (trihydroxymethyl)aminoethane; and the like. See, for example, Berge et al. (1977) J. Pharm. Sci. 66:1-19.
  • the pharmaceutically acceptable salt of oxymetazoline is oxymetazoline hydrochloride.
  • the weight percent oxymetazoline can be based on the oxymetazoline component alone.
  • the weight percent oxymetazoline can be based on the oxymetazoline salt.
  • the administering is administering as a single drop.
  • the drop can be dispensed, for example, from a suitably constructed squeeze bottle or from a dropper.
  • a single drop typically has a volume of about 0.1 to 0.35 milliliters (mL).
  • the administering is performed by the subject. In one embodiment the administering is performed by an individual other than the subject, e.g., by a health care provider, a parent, or a spouse.
  • the administering is administering at least once daily.
  • the invention contemplates administration once, twice, three times, and up to four times in any given 24 hour period.
  • the administering can be performed over equal periods, for example every twelve hours, or unequal periods, for example at 7 a.m. and 3 p.m. (rather than 7 a.m. and 7 p.m.).
  • the administering is administering once daily.
  • the subject does not have an allergic ocular condition calling for treatment of the eye with oxymetazoline. In one embodiment the subject does not have eyelid swelling. In one embodiment the subject has not undergone refractive eye surgery. In one embodiment the subject does not have an allergic ocular condition calling for treatment of the eye with oxymetazoline and the subject does not have eyelid swelling. In one embodiment the subject does not have an allergic ocular condition calling for treatment of the eye with oxymetazoline and the subject has not undergone refractive eye surgery. In one embodiment the subject does not have eyelid swelling and the subject has not undergone refractive eye surgery.
  • the subject does not have an allergic ocular condition calling for treatment of the eye with oxymetazoline, does not have eyelid swelling, and has not undergone refractive eye surgery.
  • the subject does not have acute allergic conjunctivitis or non-infectious conjunctivitis.
  • An aspect of the invention is a method for treating ptosis in a subject.
  • the method includes the step of administering an effective amount of a long-acting alpha adrenergic agonist and an effective amount of a short-acting alpha adrenergic agonist to the exterior surface of an eye of a subject in need of such treatment.
  • a “long-acting alpha adrenergic agonist” is an alpha adrenergic agonist with a systemic half-life in normal adult humans of greater than three hours.
  • Long-acting alpha adrenergic agonists include, without limitation, oxymetazoline, methoxamine, naphazoline, tetrahydrozoline, xylometazoline, and apraclonidine (also known as Iopidine®). The longest acting of these agents is oxymetazoline, with a reported half-life of 5 to 6 hours.
  • the long-acting alpha adrenergic agonist is a pharmaceutically acceptable salt of the long-acting alpha adrenergic agonist.
  • the long-acting alpha adrenergic agonist is oxymetazoline or a pharmaceutically acceptable salt thereof, e.g., oxymetazoline hydrochloride.
  • a “short-acting alpha adrenergic agonist” is an alpha adrenergic agonist with a systemic half-life in normal adult humans of less than or equal to three hours.
  • Short-acting alpha adrenergic agonists include, without limitation, phenylephrine and brimonidine.
  • the short-acting alpha adrenergic agonist is a pharmaceutically acceptable salt of the short-acting alpha adrenergic agonist.
  • the short-acting alpha adrenergic agonist is phenylephrine or a pharmaceutically acceptable salt thereof, e.g., phenylephrine hydrochloride.
  • Phenylephrine is frequently used in pre-surgical evaluation of ptosis. Typically, to predict what result might be expected from surgical treatment of ptosis, a single drop of phenylephrine 2.5% is placed in the affected eye. There is a rapid (nearly immediate) response with lifting of the lid. However, this pharmacological response lasts for less than one hour, and it may include dilation of the pupil of the treated eye.
  • Example 8 it was found that a combination of oxymetazoline, e.g., 0.1%, together with phenylephrine, e.g., 0.25%, unexpectedly acts synergistically in the treatment of ptosis.
  • the effect of the combination is dramatically greater than not only the effect of either agent alone but also the sum of the effects of each agent alone. This synergistic effect was found to occur even with a combination including an amount of phenylephrine that induces, at most, only a minimal amount of mydriasis, i.e., clinically insignificant mydriasis.
  • the long-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising at least 0.1 weight percent oxymetazoline and the short-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising at least 0.15 weight percent phenylephrine. In one embodiment the long-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising at least 0.1 weight percent oxymetazoline and the short-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising at least 0.25 weight percent phenylephrine.
  • the long-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising 0.1 weight percent oxymetazoline and the short-acting alpha adrenergic agonist is provided as a pharmaceutical composition comprising 0.25 weight percent phenylephrine.
  • oxymetazoline is formulated together with phenylephrine as a pharmaceutical composition comprising at least 0.05 weight percent oxymetazoline and at least 0.15 weight percent phenylephrine in an ophthalmologically acceptable carrier.
  • oxymetazoline is formulated together with phenylephrine as a pharmaceutical composition comprising at least 0.1 weight percent oxymetazoline and at least 0.15 percent phenylephrine in an ophthalmologically acceptable carrier. In one embodiment the oxymetazoline is formulated together with the phenylephrine as a pharmaceutical composition comprising at least 0.1 weight percent oxymetazoline and at least 0.25 weight percent phenylephrine in an ophthalmologically acceptable carrier. In one embodiment the oxymetazoline is formulated together with the phenylephrine as a pharmaceutical composition comprising 0.1 weight percent oxymetazoline and 0.25 weight percent phenylephrine in an ophthalmologically acceptable carrier.
  • the oxymetazoline is present at a concentration of at least 0.1 weight percent. In various embodiments the oxymetazoline may be present at a concentration of 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, or 1.0 weight percent, or any concentration therebetween. In one embodiment the oxymetazoline is present at a concentration of 0.1 weight percent.
  • the phenylephrine is present at a concentration of 0.15 to 1.5 weight percent. Accordingly, in various embodiments the phenylephrine can be present at a concentration of 0.15, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.1, 1.2, 1.3, 1.4, or 1.5 weight percent, or any concentration therebetween. In one embodiment the phenylephrine is present at a concentration of 0.25 weight percent.
  • An aspect of the invention is a pharmaceutical composition, comprising oxymetazoline, a short-acting alpha adrenergic agonist, and a pharmaceutically acceptable carrier, formulated for topical ophthalmic use.
  • the oxymetazoline is provided as a pharmaceutically acceptable salt, e.g., oxymetazoline hydrochloride.
  • the short-acting alpha adrenergic agonist is phenylephrine or a pharmaceutically acceptable salt thereof, e.g., phenylephrine hydrochloride.
  • the oxymetazoline is present at a concentration of at least 0.1 weight percent. In various embodiments the oxymetazoline may be present at a concentration of 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, or 1.0 weight percent, or any concentration therebetween. In one embodiment the oxymetazoline is present at a concentration of 0.1 weight percent.
  • the phenylephrine is present at a concentration of 0.15 to 1.5 weight percent. Accordingly, in various embodiments the phenylephrine can be present at a concentration of 0.15, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, 0.8, 0.9, 1.0, 1.1, 1.2, 1.3, 1.4, or 1.5 weight percent, or any concentration therebetween. In one embodiment the phenylephrine is present at a concentration of 0.25 weight percent.
  • the oxymetazoline is present at a concentration of at least 0.1 weight percent and the phenylephrine is present at a concentration of at least 0.25 weight percent.
  • the oxymetazoline is present at a concentration of 0.1 weight percent and the phenylephrine is present at a concentration of 0.25 weight percent.
  • the pharmaceutical composition optionally can include at least one additional active agent.
  • the pharmaceutical composition further includes an anti-oxidant.
  • An antioxidant is a molecule capable of inhibiting the oxidation of other molecules. Oxidation is a chemical reaction that transfers electrons from a substance to an oxidizing agent. Oxidation reactions can produce free radicals. In turn, these radicals can start chain reactions that damage cells. Antioxidants terminate these chain reactions by removing free radical intermediates, and inhibit other oxidation reactions. They do this by being oxidized themselves, so antioxidants are often reducing agents such as thiols, ascorbic acid or polyphenols.
  • Antioxidants are classified into two broad divisions, depending on whether they are soluble in water (hydrophilic) or in lipids (hydrophobic). In general, water-soluble antioxidants react with oxidants in the cell cytosol and the blood plasma, while lipid-soluble antioxidants protect cell membranes from lipid peroxidation.
  • Water-soluble antioxidants include, without limitation, ascorbic acid (vitamin C), glutathione, lipoic acid, and uric acid.
  • Lipid-soluble antioxidants include, without limitation, carotenes (e.g., alpha-carotene, beta-carotene), alpha-tocopherol (vitamin E), and ubiquinol (coenzyme Q).
  • the antioxidant is N-acetylcarnosine. In one embodiment the antioxidant is sodium metabisulfite.
  • the pharmaceutical composition further includes vitamin A (retinol).
  • vitamin A When converted to the retinal (retinaldehyde) form, vitamin A is essential for vision, and when converted to retinoic acid, is essential for skin health and bone growth.
  • These chemical compounds are collectively known as retinoids, and possess the structural motif of all-trans retinol as a common feature in their structure.
  • Topical vitamin A for example in the form of eye drops containing retinyl palmitate 0.05 percent, has been reported to be effective treatment for dry eye (also known as keratoconjunctivitis sicca, xerophthalmia, and dry eye syndrome). Kim et al. (2009) Am J Ophthalmol 147:206-13. Vitamin A has also been formulated at a strength of 50,000 units/mL for ophthalmic use.
  • the pharmaceutical composition further includes an astringent.
  • Astringents include, but are not limited to, witch hazel, zinc sulfate, silver sulfate, plant tannins, oak bark extract, bird cherry extract, and natural flavinoids.
  • the astringent is witch hazel, which is an astringent produced from the leaves and bark of the North American Witch Hazel shrub ( Hamamelis virginiana ), which grows naturally from Nova Scotia west to Ontario, Canada, and south to Florida and Texas in the United States.
  • Witch hazel is readily available from a number of commercial suppliers, including Dickinson's and Henry Thayer.
  • the pharmaceutical composition optionally can include at least one additional inert or non-active agent.
  • the pharmaceutical composition further includes a lubricant.
  • Ocular lubricants are solutions, gels, or ointments formulated to moisturize the eyes. Included among ocular lubricants are artificial tears, such as are available from any of a variety of commercial suppliers.
  • such lubricants typically may include an aqueous solution of a polyalcohol (polyol) such as polyvinyl alcohol, borate, and a buffer.
  • ocular lubricants may include white petrolatum and mineral oil.
  • the pharmaceutical composition further includes a blue dye, e.g., methylene blue.
  • a blue dye e.g., methylene blue.
  • the blue dye confers a lightening or whitening effect on the sclera, thereby making “tired eyes” appear less tired.
  • pharmaceutically acceptable carrier refers to, for example, pharmaceutically acceptable materials, compositions or vehicles, such as a liquid or solid filler, diluent, excipient, solvent or encapsulating material, involved in carrying or transporting any supplement or composition, or component thereof, from one organ, or portion of the body, to another organ, or portion of the body.
  • a pharmaceutically acceptable carrier is non-pyrogenic.
  • materials which may serve as pharmaceutically acceptable carriers include: pyrogen-free water; aqueous solutions, suspensions, and ointments; isotonic saline; Ringer's solution; phosphate buffer solutions; borate solutions; sugars, such as lactose, glucose and sucrose; starches, such as corn starch and potato starch; cellulose, and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose and cellulose acetate; powdered tragacanth; malt; gelatin; talc; excipients, such as cocoa butter and suppository waxes; oils, such as peanut oil, cottonseed oil, sunflower oil, sesame oil, olive oil, corn oil and soybean oil; glycols, such as propylene glycol; polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; esters, such as ethyl oleate and ethyl laurate;
  • novel topical pharmaceutical compositions comprising an effective amount of one or more active agents in a pharmaceutically acceptable carrier for the treatment and prevention of ptosis and/or “tired eyes”.
  • Such formulations provide a comfortable formulation when instilled in the eye.
  • the one or more active agents may include, but are not limited to, alpha adrenergic agonists and, optionally, one or more astringent agents, antioxidants, vitamin A, and any combination thereof.
  • the pharmaceutical compositions of the invention comprise one or more active ingredients formulated in an aqueous solution.
  • the pharmaceutical compositions may be formulated for topical administration as solutions, suspensions, oils, viscous or semi-viscous gels, emulsions, liposomes, lotions, ointments, creams, gels, salves, powders, and sustained or slow release, or other types of solid or semi-solid compositions, including formulations described in U.S. Pat. No. 6,806,364.
  • the compositions may also be topically administered in a sprayable form.
  • the pharmaceutical compositions includes a tear substitute.
  • tear substitutes are known in the art, including but not limited to: polyols such as, glycerol, glycerin, polyethylene glycol 300, polyethylene glycol 400, polysorbate 80, propylene glycol, and ethylene glycol, polyvinyl alcohol, povidone, and polyvinylpyrrolidone; cellulose derivatives such hydroxypropyl methylcellulose (also known as hypromellose), carboxy methylcellulose sodium, hydroxypropyl cellulose, hydroxyethyl cellulose, and methylcellulose; dextrans such as dextran 70; water soluble proteins such as gelatin; carbomers such as carbomer 934P, carbomer 941, carbomer 940 and carbomer 974P; and gums such as HP-guar.
  • polyols such as, glycerol, glycerin, polyethylene glycol 300, polyethylene glycol 400, polysorbate 80, propylene glycol, and
  • tear substitutes are commercially available, which include, but are not limited to cellulose esters such as Bion Tears®, Celluvisc®, Genteal®, OccuCoat®, Refresh® Teargen II®, Tears Naturale®, Tears Naturale 118®, Tears Naturale Free®, and TheraTears®; and polyvinyl alcohols such as Akwa Tears®, HypoTears®, Moisture Eyes®, Murine Lubricating®, and Visine Tears®.
  • the tear substitute is that which is described in U.S. Pat. No. 6,806,364, which is expressly incorporated by reference herein in its entirety. The formulation described in U.S. Pat. No.
  • 6,806,364 contains 0.2 to 2.5 (e.g., 0.5 to 0.8) percent by weight of hydroxypropyl methylcellulose, 0.045 to 0.065 (e.g., 0.05 to 0.06) percent by weight a calcium salt, and 0.14 to 1.4 (e.g., 0.3 to 1.2) percent by weight a phosphate salt.
  • the formulation described in U.S. Pat. No. 6,806,364 has a viscosity of 20 to 150 (e.g., 50 to 90) centipoise and is buffered to a pH 5.5 to 8.5 (e.g., 6 to 8) with a phosphate salt or other suitable salts.
  • Tear substitutes may also be comprised of paraffins, such as the commercially available Lacri-Lube® ointments. Other commercially available ointments that are used as tear substitutes include Lubrifresh PM®, Moisture Eyes PM, and Refresh PM.
  • compositions may be formulated for topical administration as solutions, suspensions, oils, viscous or semi-viscous gels, emulsions, liposomes, lotions, ointments, creams, gels, salves, powders, and sustained or slow release, or other types of solid or semi-solid compositions, including formulations described in U.S. Pat. No. 6,806,364.
  • the composition may also be topically administered in a sprayable form.
  • any of a variety of carriers may be used in the formulations of the present invention, including water, mixtures of water and water-miscible solvents, such as, but not limited to, C1- to C7-alkanols, vegetable oils or mineral oils comprising from 0.5 to 5% non-toxic water-soluble polymers, natural products, such as gelatin, alginates, pectins, tragacanth, karaya gum, xanthan gum, carrageenin, agar and acacia, starch derivatives, such as starch acetate and hydroxypropyl starch, and also other synthetic products, such as polyvinyl alcohol, polyvinylpyrrolidone, polyvinyl methyl ether, polyethylene oxide, preferably cross-linked polyacrylic acid, such as neutral Carbopol, or mixtures of those polymers.
  • the concentration of the carrier is, typically, from 1 to 100,000 times the concentration of the active ingredient.
  • Additional ingredients that may be included in the formulation include tonicity enhancers, preservatives, solubilizers, non-toxic excipients, demulcents, sequestering agents, pH adjusting agents, co-solvents and viscosity building agents.
  • buffers may be especially useful.
  • the pH of the present solutions should be maintained within the range of 4.0 to 8.0, more preferably about 4.0 to 6.0, more preferably about 6.5 to 7.8.
  • Suitable buffers may be added, such as, but not limited to, boric acid, sodium borate, potassium citrate, citric acid, sodium bicarbonate, TRIS, and various mixed phosphate buffers (including combinations of Na 2 HPO 1 , NaH 2 PO 4 , and KHPO 4 ) and mixtures thereof.
  • buffers will be used in amounts ranging from about 0.05 to 2.5 percent by weight, and preferably, from 0.1 to 1.5 percent.
  • Tonicity is adjusted, if needed, typically by tonicity enhancing agents.
  • Such agents may, for example, be of ionic and/or non-ionic type.
  • ionic tonicity enhancers include, but are not limited to, alkali metal or alkaline earth metal halides, such as, for example, CaCl 2 , KBr, KCl, LiCl, Na, NaBr, NaCl, Na 2 SO 4 , or boric acid.
  • Non-ionic tonicity enhancing agents are, for example, urea, glycerol, sorbitol, mannitol, propylene glycol, or dextrose. These agents may also serve as the active agents in certain embodiments.
  • aqueous solutions of the present invention are typically adjusted with tonicity agents to approximate the osmotic pressure of normal lachrymal fluids which is equivalent to a 0.9% solution of sodium chloride or a 2.5% solution of glycerol.
  • An osmolality of about 225 to 400 mOsm/kg is preferred, more preferably 280 to 320 mOsm.
  • the topical formulations additionally comprise a preservative.
  • a preservative may typically be selected from a quaternary ammonium compound such as benzalkonium chloride (N-benzyl-N—(C8-C18 alkyl)-N,N-dimethylammonium chloride), benzoxonium chloride, or the like.
  • preservatives different from quaternary ammonium salts are alkyl-mercury salts of thiosalicylic acid, such as, for example, thimerosal (also known as thiomersal), phenylmercuric nitrate, phenylmercuric acetate or phenylmercuric borate, sodium perborate, sodium chlorite, parabens, such as, for example, methylparaben or propylparaben, alcohols, such as, for example, chlorobutanol, benzyl alcohol or phenyl ethanol, guanidine derivatives, such as, for example, chlorohexidine or polyhexamethylene biguanide, sodium perborate, Germal® II or sorbic acid.
  • thiosalicylic acid such as, for example, thimerosal (also known as thiomersal), phenylmercuric nitrate, phenylmercuric acetate or phenyl
  • Preferred preservatives are quaternary ammonium compounds, in particular benzalkonium chloride or its derivative such as Polyquad (see U.S. Pat. No. 4,407,791), alkyl-mercury salts and parabens. Where appropriate, a sufficient amount of preservative is added to the ophthalmic composition to ensure protection against secondary contaminations during use caused by bacteria and fungi.
  • topical formulations of this invention do not include a preservative.
  • Such formulations would be useful for patients who wear contact lenses, or those who use several topical ophthalmic drops and/or those with an already compromised ocular surface (e.g. dry eye) wherein limiting exposure to a preservative may be desirable.
  • the topical formulation may additionally include a solubilizer, in particular if the active or the inactive ingredients tend to form a suspension or an emulsion.
  • a solubilizer suitable for an above-concerned composition is for example selected from the group consisting of tyloxapol, fatty acid glycerol polyethylene glycol esters, fatty acid polyethylene glycol esters, polyethylene glycols, glycerol ethers, a cyclodextrin (for example alpha-, beta- or gamma-cyclodextrin, e.g.
  • solubilizer is a reaction product of castor oil and ethylene oxide, for example the commercial products Cremophor EL®, or Cremophor RH40®.
  • solubilizers that are tolerated extremely well by the eye.
  • Another preferred solubilizer is selected from tyloxapol and from a cyclodextrin.
  • concentration used depends especially on the concentration of the active ingredient.
  • the amount added is typically sufficient to solubilize the active ingredient.
  • the concentration of the solubilizer is from 0.1 to 5000 times the concentration of the active ingredient.
  • the formulations may comprise further non-toxic excipients, such as, for example, emulsifiers, wetting agents or fillers, such as, for example, the polyethylene glycols designated 200, 300, 400 and 600, or Carbowax designated 1000, 1500, 4000, 6000 and 10000.
  • excipients such as, for example, emulsifiers, wetting agents or fillers, such as, for example, the polyethylene glycols designated 200, 300, 400 and 600, or Carbowax designated 1000, 1500, 4000, 6000 and 10000.
  • the amount and type of excipient added is in accordance with the particular requirements and is generally in the range of from approximately 0.0001 to approximately 90% by weight.
  • viscosity enhancing agents include, but are not limited to: polysaccharides, such as hyaluronic acid and its salts, chondroitin sulfate and its salts, dextrans, various polymers of the cellulose family; vinyl polymers; and acrylic acid polymers.
  • any compound of the present invention will vary depending on the symptoms, age, and other physical characteristics of the patient, the nature and severity of the disorder to be treated or prevented, the degree of comfort desired, the route of administration, and the form of the medicament. Any of the subject formulations may be administered in a single dose or in divided doses. Dosages for the formulations of the present invention may be readily determined by techniques known to those of skill in the art or as taught herein.
  • an effective dose or amount, and any possible effects on the timing of administration of the formulation may need to be identified for any particular formulation of the present invention. This may be accomplished by routine experiment as described herein.
  • the effectiveness of any formulation and method of treatment or prevention may be assessed by administering the formulation and assessing the effect of the administration by measuring one or more indices associated with the efficacy of the agent and with the degree of comfort to the patient, as described herein, and comparing the post-treatment values of these indices to the values of the same indices prior to treatment or by comparing the post-treatment values of these indices to the values of the same indices using a different formulation.
  • the precise time of administration and amount of any particular formulation that will yield the most effective treatment in a given patient will depend upon the activity, pharmacokinetics, and bioavailability of a particular compound, physiological condition of the patient (including age, sex, disease type and stage, general physical condition, responsiveness to a given dosage and type of medication), and the like.
  • the guidelines presented herein may be used to optimize the treatment, e.g., determining the optimum time and/or amount of administration, which will require no more than routine experimentation consisting of monitoring the subject and adjusting the dosage and/or timing.
  • compositions of the present invention may reduce the required dosage for any individual component because the onset and duration of effect of the different components may be complimentary or even synergistic.
  • the different agents may be delivered together or separately, and simultaneously or at different times within the day.
  • the formulations of the present invention may be packaged as either a single-dose product or a multi-dose product.
  • the single-dose product is sterile prior to opening of the package and all of the composition in the package is intended to be consumed in a single application to one or both eyes of a patient.
  • the use of an antimicrobial preservative to maintain the sterility of the composition after the package is opened is optional.
  • Multi-dose products are also sterile prior to opening of the package.
  • the container for the composition may be opened many times before all of the composition in the container is consumed, the multi-dose products typically have sufficient antimicrobial activity to ensure that the compositions will not become contaminated by microbes as a result of the repeated opening and handling of the container.
  • the level of antimicrobial activity required for this purpose is well known to those skilled in the art, and is specified in official publications, such as the United States Pharmacopoeia (“USP”), other publications by the Food and Drug Administration, and corresponding publications in other countries. Detailed descriptions of the specifications for preservation of ophthalmic pharmaceutical products against microbial contamination and the procedures for evaluating the preservative efficacy of specific formulations are provided in those publications. In the United States, preservative efficacy standards are generally referred to as the “USP PET” requirements. (The acronym “PET” stands for “preservative efficacy testing”.)
  • a single-dose packaging arrangement eliminates the need for an antimicrobial preservative in the compositions, which is a significant advantage from a medical perspective, because conventional antimicrobial agents utilized to preserve ophthalmic compositions (e.g., benzalkonium chloride) may cause ocular irritation, particularly in patients suffering from dry eye conditions or pre-existing ocular irritation.
  • conventional antimicrobial agents utilized to preserve ophthalmic compositions e.g., benzalkonium chloride
  • the single-dose packaging arrangements currently available such as small volume plastic vials prepared by means of a process known as “form, fill and seal”, have several disadvantages for manufacturers and consumers.
  • the principal disadvantages of the single-dose packaging systems are the much larger quantities of packaging materials required, which is both wasteful and costly, and the inconvenience for the consumer.
  • formulations of this invention are preferably formulated as “ready for use” aqueous solutions
  • alternative formulations are contemplated within the scope of this invention.
  • the active ingredients, surfactants, salts, chelating agents, or other components of the ophthalmic solution, or mixtures thereof can be lyophilized or otherwise provided as a dried powder or tablet ready for dissolution (e.g., in deionized, or distilled) water.
  • kits for the packaging and/or storage and/or use of the formulations described herein, as well as kits for the practice of the methods described herein.
  • kits may comprise one or more containers containing one or more ophthalmic preparations, tablets, or capsules of this invention.
  • the kits can be designed to facilitate one or more aspects of shipping, use, and storage.
  • kits may optionally include instructional materials containing directions (i.e., protocols) disclosing means of use of the formulations provided therein. While the instructional materials typically comprise written or printed materials, they are not limited to such. Any medium capable of storing such instructions and communicating them to an end user is contemplated by this invention. Such media include, but are not limited to electronic storage media (e.g., magnetic discs, tapes, cartridges, chips), optical media (e.g., CD ROM), and the like. Such media may include addresses to internet sites that provide such instructional materials.
  • electronic storage media e.g., magnetic discs, tapes, cartridges, chips
  • optical media e.g., CD ROM
  • a single drop of 0.1% oxymetazoline solution was placed in the affected eye of each of five adult human subjects with unilateral ptosis.
  • Palpebral fissure was measured at baseline (pre-treatment), then at 30 minutes and at 4 hours following treatment. Measurements were taken with a fine point metric ruler, measuring (in mm) the central diameter of the palpebral fissure (i.e., sagitally across the center of the pupil). Results are shown in Table 1. “OD” refers to right eye; “OS” refers to left eye. “Rx” refers to which eye was treated. “% ⁇ (4 hr)” is the percent change 4 hours following treatment. All measurements are reported in mm.
  • a single drop of 0.1% oxymetazoline solution was randomly assigned to be placed in one eye of each of five normal adult human subjects; a single drop of vehicle alone (negative control) was placed in the other eye of each subject.
  • Palpebral fissure was measured at baseline (pre-treatment), then at 1 hour and at 4 hours following treatment. Measurements were taken with a fine point metric ruler, measuring (in mm) the central diameter of the palpebral fissure (i.e., sagitally across the center of the pupil). Results are shown in Table 2. “OD” refers to right eye; “OS” refers to left eye. “Rx” refers to treatment. “Oxy” refers to oxymetazoline; “V” refers to vehicle.
  • % ⁇ (4 hr) is the percent change 4 hours following treatment. All measurements are reported in mm. As shown in Table 2, 0.1% oxymetazoline vertically widened the palpebral fissure in 5/5 (100%) of subjects, and this effect lasted at least 4 hours. The mean increase from baseline, 4 hours following treatment, was 1.4 mm or 15.4%.
  • a single drop of 0.1% oxymetazoline solution was randomly assigned to be placed in one eye of each of ten normal adult human subjects; a single drop of 0.025% oxymetazoline (Visine® L.R.®, positive control) was placed in the other eye of each subject.
  • Palpebral fissure was measured at baseline (pre-treatment), then at minutes and at 3 hours following treatment. Measurements were taken with a fine point metric ruler, measuring (in mm) the central diameter of the palpebral fissure (i.e., sagitally across the center of the pupil). Results are shown in Table 3. “OD” refers to right eye; “OS” refers to left eye. “Rx” refers to treatment.
  • Oxy refers to 0.1% oxymetazoline; “Vis” refers to Visine® L.R.® (0.025% oxymetazoline). “% ⁇ (3 hr)” is the percent change 3 hours following treatment. All measurements are reported in mm. As shown in Table 3, 0.1% oxymetazoline vertically widened the palpebral fissure to a greater extent than did 0.025% oxymetazoline (Visine® L.R.®) in 9/10 (90%) of subjects. The mean change from baseline, 3 hours following treatment with 0.1% oxymetazoline, was 1 mm or 11.2%. The mean change from baseline, 3 hours following treatment with 0.025% oxymetazoline, was ⁇ 0.1 mm or ⁇ 0.8%.
  • the negative mean change for subjects receiving 0.025% oxymetazoline reflects Hering's Law of equal innervation, whereby the upper eyelid with a weaker stimulus (e.g., 0.025% oxymetazoline) will tend to drop, while the eyelid with the stronger stimulus (e.g., 0.1% oxymetazoline) will elevate.
  • a weaker stimulus e.g. 0.025% oxymetazoline
  • the stronger stimulus e.g. 0.1% oxymetazoline
  • Oxymetazoline Single Drop Administration of 0.1% Oxymetazoline v. Repeated Administration of 0.025% Oxymetazoline (Visine®® L.R.®)
  • a subject with pronounced ptosis of both eyelids was treated with a single drop of Visine® L.R.® to each eye, followed 15 minutes later by administration of a second single drop of Visine® L.R.® to each eye. Photographs of the subject's face were taken before the first and second treatments and again 30 minutes after the first dose. There was little or no response to the first or second treatments. Some days later, the same subject was treated with a single drop of oxymetazoline 0.1% to each eye. Photographs of the subject's face were taken before treatment and then minutes following treatment. Results are shown in FIG. 1 . The top panel shows the subject prior to receiving the single drop of 0.1% oxymetazoline to each eye.
  • the middle panel shows the subject 30 minutes after receiving the single drop of 0.1% oxymetazoline to each eye.
  • the bottom is panel shows the subject 90 minutes after receiving the single drop of 0.1% oxymetazoline to each eye. This example shows that treatment with a single drop of 0.1% oxymetazoline is dramatically more effective than repeated administration of 0.025% oxymetazoline.
  • a subject with moderate ptosis of the left eyelid was treated with a single drop of 0.1% oxymetazoline administered topically to the left eye. Photographs of her face were taken before and then 25 minutes and 3.5 hours after treatment. Results are shown in FIG. 2 . As shown in the figure, the ptosis was dramatically improved, in fact essentially resolved during the period of observation, following treatment with the single drop of 0.1% oxymetazoline. Although not shown in FIG. 2 , the effect lasted at least six hours.
  • a normal adult human subject was treated with a single drop of a combination formulation of 0.1% oxymetazoline and 1.25% phenylephrine to both eyes. Photographs of the subject's face were taken before treatment and then 30 minutes and 45 minutes following treatment. Both eyes were wider, and both pupils were mildly dilated, at 30 and 45 minutes after treatment.
  • a second normal adult human subject was treated with a single drop of 0.1% oxymetazoline to the right eye, and a single drop of a combination formulation of 0.1% oxymetazoline and 1.25% phenylephrine to the left eye. Photographs of the subject's face were taken before treatment and then 30 minutes and 45 minutes following treatment. Both eyes were wider, with the left eye visibly wider than the right eye, 30 and 45 minutes after treatment. The pupil of the left eye was mildly dilated following treatment as compared to before treatment and as compared to the pupil of the right following treatment.
  • a single drop of 0.11% oxymetazoline solution was placed in each eye of six normal subjects. Pupils were measured at baseline and 30 minutes following administration of oxymetazoline. Results are shown in Table 4. “OD” refers to right eye; “OS” refers to left eye. “Baseline” refers to before treatment. “30 min” refers to 30 minutes following administration of 0.1% oxymetazoline). All measurements are reported in mm.
  • Results shown in Tables 5 and 6 can be summarized as follows.
  • the combination of oxymetazoline 0.1% and phenylephrine 0.25% (“combo”) caused a 20% increase in lid aperture; in contrast, oxymetazoline 0.1% alone (“oxy”) caused a 7%/increase in lid aperture and phenylephrine 0.25% alone (“phe”) caused only a 2% increase in lid aperture.
  • the combination of oxymetazoline 0.1% and phenylephrine 0.25% caused a 21% increase in lid aperture, whereas oxymetazoline 0.1% alone caused a 3% increase in lid aperture and phenylephrine 0.25% alone caused a 4% increase in lid aperture.
  • mean pupil change with the combination of oxymetazoline 0.1% and phenylephrine 0.25% was 0.4 mm; in contrast, mean pupil change for oxymetazoline 0.1% alone was 0 mm and for phenylephrine 0.25% alone was 0.4 mm.
  • the combination drop exerted a more profound effect on lid separation than either of the two components alone.
  • the combination drop exerted a more profound effect on lid separation than the sum of the effects of the two components alone, i.e., the combination of oxymetazoline 0.1% and phenylephrine 0.25% exerted a synergistic effect.
  • Visual field refers to the area projected onto the retina of and perceived by an eye.
  • a visual field test a patient places his or her face in a little “dome” and stares at a central light. Smaller target lights illuminate in the peripheral parts of the dome, and the patient clicks a button every time he or she sees a target light.
  • a computer records the is number (and location) of spots seen versus not seen.
  • the test can be summarized in terms of the percent of target lights seen by each eye. For example, in a visual field test with 36 target lights, a score of 25% for the left eye would indicate that only one quarter (9) of the target lights were seen with the left eye.
  • a 78-year-old woman with bilateral ptosis and dense inferior visual field defects in both eyes due to glaucoma was administered a single drop of 0.1% oxymetazoline to each eye. She had essentially lost the bottom half of her vision from glaucoma (not reversible), and the top half of her vision from ptosis. Treatment with 0.1% oxymetazoline temporarily restored the top parts of her visual fields by relieving her bilateral ptosis.

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US13/218,584 US20120225918A1 (en) 2011-03-03 2011-08-26 Compositions and Methods for Non-Surgical Treatment of Ptosis
US13/270,577 US8357714B2 (en) 2011-03-03 2011-10-11 Compositions and methods for non-surgical treatment of ptosis
PL12709421T PL2680829T3 (pl) 2011-03-03 2012-02-24 Kompozycje i sposoby niechirurgicznego leczenia ptozy
DK12709421T DK2680829T3 (da) 2011-03-03 2012-02-24 Sammensætninger og metoder til ikke-kirurgisk behandling af ptosis
CN201280011433.6A CN103501771B (zh) 2011-03-03 2012-02-24 用于上睑下垂的非手术治疗的组合物和方法
PT127094217T PT2680829T (pt) 2011-03-03 2012-02-24 Composições e métodos para tratamento não cirúrgico de ptose
LTEP12709421.7T LT2680829T (lt) 2011-03-03 2012-02-24 Kompozicijos ir būdai, skirti nechirurginiam ptozės gydymui
RU2013142602/15A RU2582392C2 (ru) 2011-03-03 2012-02-24 Композиции и способы для нехирургического лечения птоза
ES12709421T ES2750123T3 (es) 2011-03-03 2012-02-24 Composiciones y métodos para tratamiento no quirúrgico de la ptosis
BR112013022094A BR112013022094A2 (pt) 2011-03-03 2012-02-24 composições e métodos para o tratamento não cirúrgico da ptose
CA2827285A CA2827285C (en) 2011-03-03 2012-02-24 Compositions and methods for non-surgical treatment of ptosis
EP12709421.7A EP2680829B1 (en) 2011-03-03 2012-02-24 Compositions and methods for non-surgical treatment of ptosis
AU2012223615A AU2012223615B2 (en) 2011-03-03 2012-02-24 Compositions and methods for non-surgical treatment of ptosis
PCT/US2012/026496 WO2012118704A1 (en) 2011-03-03 2012-02-24 Compositions and methods for non-surgical treatment of ptosis
EP19199263.5A EP3653205A3 (en) 2011-03-03 2012-02-24 Oxymethazoline for topical ophthalmic administration and uses thereof
RS20191580A RS59636B1 (sr) 2011-03-03 2012-02-24 Kompozicije i postupci za nehirurško lečenje ptoze
NZ614719A NZ614719B2 (en) 2011-03-03 2012-02-24 Compositions and methods for non-surgical treatment of ptosis
MX2013009597A MX345042B (es) 2011-03-03 2012-02-24 Composiciones y métodos para tratamiento no quirúrgico de ptosis.
SI201231705T SI2680829T1 (sl) 2011-03-03 2012-02-24 Sestavki in metode za ne-kirurško zdravljenje ptoze
SG2013062245A SG192801A1 (en) 2011-03-03 2012-02-24 Compositions and methods for non-surgical treatment of ptosis
KR1020137026050A KR101889392B1 (ko) 2011-03-03 2012-02-24 안검하수증의 비-외과적 치료를 위한 조성물 및 방법
JP2013556744A JP6106100B2 (ja) 2011-03-03 2012-02-24 眼瞼下垂症の非外科的治療用組成物および方法
HUE12709421A HUE046740T2 (hu) 2011-03-03 2012-02-24 Készítmények és eljárások ptosis (szemhéjcsüngés) nem-mûtéti kezelésére
US13/408,364 US9018240B2 (en) 2011-03-03 2012-02-29 Compositions and methods for non-surgical treatment of ptosis
ZA2013/07262A ZA201307262B (en) 2011-03-03 2013-09-27 Compositions and methods for non-surgical treatment of ptosis
US14/625,099 US9867808B2 (en) 2011-03-03 2015-02-18 Compositions and methods for non-surgical treatment of Ptosis
US15/837,325 US20180338953A1 (en) 2011-03-03 2017-12-11 Compositions and Methods for Non-Surgical Treatment of Ptosis
US16/577,262 US10912765B2 (en) 2011-03-03 2019-09-20 Compositions and methods for non-surgical treatment of ptosis
CY20191101170T CY1122565T1 (el) 2011-03-03 2019-11-07 Συνθεσεις και μεθοδοι μη χειρουργικης θεραπειας βλεφαροπτωσης
HRP20192266TT HRP20192266T1 (hr) 2011-03-03 2019-12-17 Kompozicije i postupci za nekirurško liječenje ptoze
US16/892,645 US20200360345A1 (en) 2011-03-03 2020-06-04 Compositions and methods for non-surgical treatment of ptosis
US17/679,278 US20220218669A1 (en) 2011-03-03 2022-02-24 Compositions and methods for non-surgical treatment of ptosis

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US13/408,364 Active US9018240B2 (en) 2011-03-03 2012-02-29 Compositions and methods for non-surgical treatment of ptosis
US14/625,099 Active US9867808B2 (en) 2011-03-03 2015-02-18 Compositions and methods for non-surgical treatment of Ptosis
US15/837,325 Abandoned US20180338953A1 (en) 2011-03-03 2017-12-11 Compositions and Methods for Non-Surgical Treatment of Ptosis
US16/577,262 Active US10912765B2 (en) 2011-03-03 2019-09-20 Compositions and methods for non-surgical treatment of ptosis
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