AU2002316133A1 - Method of treating dry eye disorders - Google Patents

Description

Method of Treating Dry Eye Disorders

The present invention is directed to the treatment of dry eye disorders. In particular, the present invention is directed toward the use of 22,29-epoxy- 3,4,6,7,29-pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)-stigmastan-15-one in the treatment of dry eye and other disorders requiring the wetting of the eye in mammals.

Background of the Invention

Dry eye, also known generically as keratoconjunctivitis sicca, is a common ophthalmological disorder affecting millions of Americans each year. The condition is particularly widespread among post-menopausal women due to hormonal changes following the cessation of fertility. Dry eye may afflict an individual with varying severity. In mild cases, a patient may experience burning, a feeling of dryness, and persistent irritation such as is often caused by small bodies lodging between the eye lid and the eye surface. In severe cases, vision may be substantially impaired. Other diseases, such as Sjogren's disease and cicatricial pemphigoid manifest dry eye complications.

Although it appears that dry eye may result from a number of unrelated pathogenic causes, all presentations of the complication share a common effect, that is the breakdown of the pre-ocular tear film, which results in dehydration of the exposed outer surface and many of the symptoms outlined above (Lemp, Report of the National Eye Institute/Industry Workshop on Clinical Trials in Dry Eyes, The CLAO Journal, volume 21 , number 4, pages 221-231 (1995)).

Practitioners have taken several approaches to the treatment of dry eye. One common approach has been to supplement and stabilize the ocular tear film using so-called artificial tears instilled throughout the day. Other approaches include the use of ocular inserts that provide a tear substitute or stimulation of endogenous tear production.

Examples of the tear substitution approach include the use of buffered, isotonic saline solutions, aqueous solutions containing water soluble polymers that render the solutions more viscous and thus less easily shed by the eye. Tear reconstitution is also attempted by providing one or more components of the tear film such as phospholipids and oils. Phospholipid compositions have been shown to be useful in treating dry eye; see, e.g., McCulley and Shine, Tear film structure and dry eye, Contactologia, volume 20(4), pages 145-49 (1998); and Shine and McCulley, Keratoconjunctivitis sicca associated with meibomian secretion polar lipid abnormality, Archives of Ophthalmology, volume 116(7), pages 849-52 (1998). Examples of phospholipid compositions for the treatment of dry eye are disclosed in U.S. Patent Nos. 4,131 ,651 (Shah et al.), 4,370,325 (Packman), 4,409,205 (Shively), 4,744,980 and 4,883,658 (Holly), 4,914,088 (Glonek), 5,075,104 (Gressel et al.), 5,278,151 (Korb et al.), 5,294,607 (Glonek et al.), 5,371 ,108 (Korb et al.) and 5,578,586 (Glonek et al.). U.S. Patent No. 5,174,988 (Mautone et al.) discloses phospholipid drug delivery systems involving phospholipids, propellants and an active substance.

Another approach involves the provision of lubricating substances in lieu of artificial tears. For example, U.S. Patent No. 4,818,537 (Guo) discloses the use of a lubricating, liposome-based composition, and U.S. Patent No. 5,800,807 (Hu et al.) discloses compositions containing glycerin and propylene glycol for treating dry eye.

Although these approaches have met with some success, problems in the treatment of dry eye nevertheless remain. The use of tear substitutes, while temporarily effective, generally requires repeated application over the course of a patient's waking hours. It is not uncommon for a patient to have to apply artificial tear solution ten to twenty times over the course of the day. Such an undertaking is not only cumbersome and time consuming, but is also potentially very expensive. Transient symptoms of dry eye associated with refractive surgery have been reported to last in some cases from six weeks to six months or more following surgery.

Aside from efforts directed primarily to the alleviation of symptoms associated with dry eye, methods and compositions directed to treatment of the dry eye condition have also been pursued. For example, U.S. Patent No. 5,041 ,434 (Lubkin) discloses the use of sex steroids, such as conjugated estrogens, to treat dry eye conditions in post-menopausal women; U.S. Patent No. 5,290,572 (MacKeen) discloses the use of finely divided calcium ion compositions to stimulate pre-ocular tear film production; and U.S. Patent No. 4,966,773 (Gressel et al.) discloses the use of microfine particles of one or more retinoids for ocular tissue normalization.

Some recent literature reports suggest that patients suffering from dry eye syndrome disproportionately exhibit the hallmarks of excessive inflammation in relevant ocular tissues, such as the lacrimal and meibomian glands. The use of various compounds to treat dry eye patients, such as steroids [e.g. U.S. Patent No. 5,958,912; Marsh, et al., Topical nonpreserved methylprednisolone therapy for keratoconjunctivitis sicca in Sjogren syndrome, Ophthalmology, 106(4): 811-816 (1999); Pflugfelder, et. al. U.S. Patent No. 6,153,607], cytokine release inhibitors (Yanni, J.M.; et. al. WO 0003705 A1), cyclosporine A [Tauber, J. Adv. Exp. Med. Biol. 1998, 438 (Lacrimal Gland, Tear Film, and Dry Eye Syndromes 2), 969], and 15-HETE (Yanni et. al., US Patent No. 5,696,166), has been disclosed.

Corticosteroids, such as prednisolone, dexamethasone, fluoromethalone, hydrocortisone, loteprednol, triamcinolone, etc., cannot be used for prolonged therapy in dry eye patients without causing side effects. Steroid-related complications including increased intraocular pressure and cataract formation have been observed in dry eye patients treated with corticosteroids after several months of therapy. See Marsh, et al., Ophthalmology, 106(4): 811-816 (1999). Marsh, et al. conclude: "Because of the chronic nature of [dry eye] disease and the likelihood of patients developing steroid-related complications with their long-term use, topical nonpreserved methylprednisolone therapy appears to be most appropriate for short-term 'pulse' treatment of exacerbations of keratoconjunctivits sicca." Id. at 811.

U.S. Patent No. 6,046,185 discloses 6,7-oxygenated steroids, including 22,29-epoxy-3,4,6,7,29-pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)- stigmastan-15-one, for use in the treatment of asthma, allergy, inflammation including arthritis and thrombosis. Kuriakose, et al., J. Allergy Clin Immunol, 107(2), S97, Abstract #326, discloses that 22,29-epoxy-3,4,6,7,29- pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)-stigmastan-15-one has demonstrated significant anti-inflammatory properties, but that it has a mechanism of action distinct from that of glucocorticoids such as dexamethasone. Kuriakose, et al. conclude that despite its steroidal backbone, it is "distinctly different from a classic glucocorticoid." Neither the '185 patent nor Kuriakose, et al. mentions the use of any compounds for the topical treatment of dry eye.

Summary of the Invention

The present invention is directed to methods for the treatment of dry eye and other disorders requiring the wetting of the eye, including symptoms of dry eye associated with refractive surgery such as LASIK surgery. According to the methods of the present invention, 22,29-epoxy-3,4,6,7,29- pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)-stigmastan-15-one is administered to a patient suffering from dry eye or other disorders requiring wetting of the eye. The methods of the present invention have reduced risk of steroid- related complications compared to methods involving compounds that have a glucocorticoid's mechanism of action. The 22,29-epoxy-3,4,6,7,29- pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)-stigmastan-15-one is preferably administered topically to the eye.

Detailed Description of the Invention

22,29-epoxy-3,4,6,7,29-pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)- stigmastan-15-one is a known compound and can be synthesized by methods disclosed in U.S. Patent No. 6,046,185, the entire contents of which are hereby incorporated by reference in the present specification. This compound is also known by the code name IPL576.092.

According to the methods of the present invention, a composition comprising 22,29-epoxy-3,4,6,7,29-pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)- stigmastan-15-one and a pharmaceutically acceptable carrier for topical ophthalmic administration or implantation into the conjunctival sac or anterior chamber of the eye is administered to a mammal in need thereof. The compositions are formulated in accordance with methods known in the art for the particular route of administration desired.

The compositions administered according to the present invention comprise a pharmaceutically effective amount of 22,29-epoxy-3,4,6,7,29- pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)-stigmastan-15-one. As used herein, a "pharmaceutically effective amount" is one which is sufficient to reduce or eliminate signs or symptoms of dry eye or other disorders requiring the wetting of the eye. Generally, for compositions intended to be administered topically to the eye in the form of eye drops or eye ointments, the amount of 22,29-epoxy-3,4,6,7,29-pentahydroxy-

,(3α,4β,5α,6α,7β,14β,22S)-stigmastan-15-one will be about 0.001 to 5.0% (w/v). For preferred topically administrable ophthalmic compositions, the amount of 22,29-epoxy-3,4,6,7,29-pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)- stigmastan-15-one will be about 0.001 to 1.0% (w/v).

The compositions administered according to the present invention may also include various other ingredients, including but not limited to surfactants, tonicity agents, buffers, preservatives, co-solvents and viscosity building agents.

Various tonicity agents may be employed to adjust the tonicity of the composition, preferably to that of natural tears for ophthalmic compositions. For example, sodium chloride, potassium chloride, magnesium chloride, calcium chloride, dextrose and/or mannitol may be added to the composition to approximate physiological tonicity. Such an amount of tonicity agent will vary, depending on the particular agent to be added. In general, however, the compositions will have a tonicity agent in an amount sufficient to cause the final composition to have an ophthalmically acceptable osmolality (generally about 150 - 450 mOsm, preferably 250 - 350 mOsm).

An appropriate buffer system (e.g., sodium phosphate, sodium acetate, sodium citrate, sodium borate or boric acid) may be added to the compositions to prevent pH drift under storage conditions. The particular concentration will vary, depending on the agent employed. Preferably, however, the buffer will be chosen to maintain a target pH within the range of pH 6-7.5.

Compositions formulated for the treatment of dry eye-type diseases and disorders may also comprise aqueous carriers designed to provide immediate, short-term relief of dry eye-type conditions. Such carriers can be formulated as a phospholipid carrier or an artificial tears carrier, or mixtures of both. As used herein, "phospholipid carrier" and "artificial tears carrier" refer to aqueous compositions which: (i) comprise one or more phospholipids (in the case of phospholipid carriers) or other compounds, which lubricate, "wet," approximate the consistency of endogenous tears, aid in natural tear build-up, or otherwise provide temporary relief of dry eye symptoms and conditions upon ocular administration; (ii) are safe; and (iii) provide the appropriate delivery vehicle for the topical administration of an effective amount of 22,29- epoxy-3,4,6,7,29-pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)-stigmastan-15- one. Examples or artificial tears compositions useful as artificial tears carriers include, but are not limited to, commercial products, such as Tears Naturale®, Tears Naturale II®, Tears Naturale Free®, and Bion Tears® (Alcon Laboratories, Inc., Fort Worth, Texas). Examples of phospholipid carrier formulations include those disclosed in U.S. Patent Nos. 4,804,539 (Guo et al.), 4,883,658 (Holly), 4,914,088 (Glonek), 5,075,104 (Gressel et al.), 5,278,151 (Korb et al.), 5,294,607 (Glonek et al.), 5,371 ,108 (Korb et al.), 5,578,586 (Glonek et al.); the foregoing patents are incorporated herein by reference to the extent they disclose phospholipid compositions useful as phospholipid carriers of the present invention.

Other compounds designed to lubricate, "wet," approximate the consistency of endogenous tears, aid in natural tear build-up, or otherwise provide temporary relief of dry eye symptoms and conditions upon ocular administration the eye are known in the art. Such compounds may enhance the viscosity of the composition, and include, but are not limited to: monomeric polyols, such as, glycerol, propylene glycol, ethylene glycol; polymeric polyols, such as, polyethylene glycol, hydroxypropylmethyl cellulose ("HPMC"), carboxy methylcellulose sodium, hydroxy propylcellulose ("HPC"), dextrans, such as, dextran 70; water soluble proteins, such as gelatin; and vinyl polymers, such as, polyvinyl alcohol, polyvinylpyrrolidone, povidone and carbomers, such as, carbomer 934P, carbomer 941 , carbomer 940, carbomer 974P. Other compounds may also be added to the ophthalmic compositions of the present invention to increase the viscosity of the carrier. Examples of 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. In general, the phospholipid carrier or artificial tears carrier compositions will exhibit a viscosity of 1 to 400 centipoises ("cps").

Topical ophthalmic products are typically packaged in multidose form. Preservatives are thus required to prevent microbial contamination during use. Suitable preservatives include: benzalkonium chloride, chlorobutanol, benzododecinium bromide, methyl paraben, propyl paraben, phenylethyl alcohol, edetate disodium, sorbic acid, polyquatemium-1 , or other agents known to those skilled in the art. Such preservatives are typically employed at a level of from 0.001 to 1.0% w/v. Unit dose compositions of the present invention will be sterile, but typically unpreserved. Such compositions, therefore, generally will not contain preservatives.

The preferred compositions of the present invention are intended for administration to a human patient suffering from dry eye or symptoms of dry eye. Preferably, such compositions will be administered topically. In general, the doses used for the above described purposes will vary, but will be in an effective amount to eliminate or improve dry eye conditions. Generally, 1-2 drops of such compositions will be administered from once to many times per day.

A representative eye drop formulation is provided in Example 1 below.

Example 1

The composition of Example 1 can be prepared using a slight modification of the method disclosed in U.S. Patent No. 6,071 ,904. Briefly, a concentrated slurry of 22,29-epoxy-3,4,6,7,29-pentahydroxy-

,(3 ,4β,5α,6α,7β,14β,22S)-stigmastan-15-one in a milling bottle is autoclaved. The aqueous slurry is a mixture containing 3-mm zirconium beads, the total required amount of drug and polysorbate 80 and approximately one-half of the required amounts of benzalkonium chloride and disodium edetate. After autoclaving, the drug slurry is ball milled for approximately 18 hrs at approximately 50-55 rpm. After milling, the milling beads are removed from the milled slurry by filtration as the milled slurry is aseptically added to an autoclaved aqueous vehicle (pH adjusted to 7.2 with NaOH/HCI) containing the required amounts of sodium chloride and carbomer 974P and the remaining amounts of benzalkonium chloride, and disodium edetate. The sterile product is then adjusted to the final batch weight with sterile purified water and thoroughly mixed. This invention has been described by reference to certain preferred embodiments; however, it should be understood that it may be embodied in other specific forms or variations thereof without departing from its special or essential characteristics. The embodiments described above are therefore considered to be illustrative in all respects and not restrictive, the scope of the invention being indicated by the appended claims rather than by the foregoing description.

Claims (5)

WHAT IS CLAIMED IS:

1. A method for the treatment of dry eye and other disorders requiring the wetting of the eye which comprises administering to a mammal a composition comprising a pharmaceutically acceptable carrier and a pharmaceutically effective amount of 22,29-epoxy-3,4,6,7,29-pentahydroxy- s ,(3α,4β,5α,6α,7β,14β,22S)-stigmastan-15-one.

2. The method of Claim 1 wherein the pharmaceutically effective amount of 22,29-epoxy-3,4,6,7,29-pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)- stigmastan-15-one is 0.001 - 5.0% (w/v). 0

3. The method of Claim 2 wherein the pharmaceutically effective amount of 22,29-epoxy-3,

4,6,7,29-pentahydroxy-,(3α,4β,5α,6α,7β,14β,22S)- stigmastan-15-one is 0.001 - 1.0% (w/v).

s 4. The method of Claim 1 wherein the composition is topically administered to the eye.

5. The method of Claim 1 wherein the dry eye and other disorders requiring the wetting of the eye is symptoms of dry eye associated with 0 refractive surgery.