CYCLOSPORIN COMPOSITIONS FOR OCULAR ROSACEA TREATMENT

Abstract

Disclosed herein are methods of treating ocular rosacea with cyclosporin A. Compositions and medicaments related thereto are also disclosed.

Description

This application is a continuation of U.S. patent application Ser. No. 11/781,095, filed Jul. 20, 2007, which application is based, and claims priority under 35 U.S.C. § 120 to U.S. Provisional Application Ser. No. 60/820,239, filed Jul. 25, 2006; U.S. Provisional Application Ser. No. 60/829,796, filed Oct. 17, 2006; U.S. Provisional Application Ser. No. 60/829,808, filed Oct. 17, 2006; U.S. Provisional Application Ser. No. 60/883,525, filed Jan. 5, 2007; U.S. Provisional Application Ser. No. 60/916,352, filed May 7, 2007; and U.S. Provisional Application Ser. No. 60/869,459, filed Dec. 11, 2006; each of which is hereby incorporated by reference in their entirety.

BACKGROUND OF THE INVENTION

Rosacea is a chronic and common skin disorder with no identified cause or cure. The pathogenesis of rosacea is thought to have multiple factors. Possible factors include exposure to the demodex folliculorum mite, gastrointestinal disease or a vasodilation disorder, and other triggers such as diet or sunlight. Patients may present with a variety of symptoms, including inflammatory papules, edema, telangiectasia, rhinophyma and ocular symptoms.

The ocular signs of rosacea include blepharitis, including anterior blepharitis, conjunctivitis, iritis, iridocyclitis, keratitis, meibomian gland dysfunction, telangiectasia, erythema, chalazion, hordeolum, interpalpebral hyperemia, conjuctival hyperemia, ciliary base injection, bulbar injection, crusts, sleeves, and superficial punctuate keratopathy. The ocular symptoms are nonspecific and may include burning, tearing, decreased tear secretion, redness, and foreign body or gritty or dry sensation, irritation, Itchiness, Blurred vision, Photosensitivity, Watery eyes, bloodshot eyes, Burning, telangiectasia, irregularity of the lid margins, and meibomian gland dysfunction.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 Mean (±SD) cornea cyclosporine A concentrations (semi-log) following a single bilateral topical ocular instillation of one of three 0.05% cyclosporine A formulations to New Zealand White rabbits.

FIG. 2 Mean (±SD) conjunctiva cyclosporine A concentrations (semi-log) following a single bilateral topical ocular instillation of one of three 0.05% cyclosporine A formulations to New Zealand White rabbits.

FIG. 3 Mean (±SD) sclera cyclosporine A concentrations (semi-log) following a single bilateral topical ocular instillation of one of three 0.05% cyclosporine A formulations to New Zealand White rabbits.

FIG. 4 Mean (±SD) eyelid margin cyclosporine A (concentrations (semi-log) following a single bilateral topical ocular instillation of one of three 0.05% cyclosporine A formulations to New Zealand White rabbits.

FIG. 5 Mean (±SD) nasolacrimal duct cyclosporine A concentrations (semi-log) following a single bilateral topical ocular instillation of one of three 0.05% cyclosporine A formulations to New Zealand White rabbits.

DETAILED DESCRIPTION OF THE INVENTION

We have surprisingly discovered that aqueous compositions of cyclosporin A at a concentration of less than about 0.05% (w/v) can be prepared that will be effective in the treatment of ocular rosacea.

Cyclosporin A is a cyclic peptide with immunosuppressive properties having the structure shown above. It is also known by other names including cyclosporine, cyclosporine A, ciclosporin, and ciclosporin A.

Treatment Methods

One embodiment is a method of treating ocular rosacea comprising topically administering to a mammal in need thereof a composition comprising cyclosporin A at a concentration of from 0.0001% (w/v) to less than about 0.05% (w/v).

In one embodiment, the composition is used to treat rosacea associated lid or corneal changes.

Another method is effective for the treatment of blepharitis.

Another method is effective for the treatment of anterior blepharitis.

Another method is effective for the treatment of conjunctivitis.

Another method is effective for the treatment of iritis.

Another method is effective for the treatment of iridocyclitis.

Another method is effective for the treatment of keratitis.

Another method is effective for the treatment of meibomian gland dysfunction.

Another method is effective for the treatment of telangiectasia.

Another method is effective for the treatment of erythema.

Another method is effective for the treatment of chalazion.

Another method is effective for the treatment of hordeolum.

Another method is effective for the treatment of interpalpebral hyperemia.

Another method is effective for the treatment of conjuctival hyperemia.

Another method is effective for the treatment of ciliary base injection.

Another method is effective for the treatment of bulbar injection.

Another method is effective for the treatment of crusts.

Another method is effective for the treatment of sleeves.

Another method is effective for the treatment of superficial punctuate.

Another method is effective for the treatment of keratopathy.

Another method is effective for the treatment of burning.

Another method is effective for the treatment of tearing.

Another method is effective for the treatment of decreased tear secretion.

Another method is effective for the treatment of redness.

Another method is effective for the treatment of foreign body sensation.

Another method is effective for the treatment of gritty sensation.

Another method is effective for the treatment of dry sensation.

Another method is effective for the treatment of irritation.

Another method is effective for the treatment of itchiness.

Another method is effective for the treatment of blurred vision.

Another method is effective for the treatment of photosensitivity.

Another method is effective for the treatment of watery eyes.

Another method is effective for the treatment of bloodshot eyes.

Another method is effective for the treatment of burning.

Another method is effective for the treatment of telangiectasia.

Another method is effective for the treatment of irregularity of the lid margins.

Another method is effective for the treatment of meibomian gland dysfunction.

For the purposes of this disclosure, “treat,” “treating,” or “treatment” refer to the use of a compound, composition, therapeutically active agent, or drug in the diagnosis, cure, mitigation, treatment, prevention of disease or other undesirable condition, or to affect the structure or any function of the body of man or other animals.

The treatment generally comprises administering 10-50 μL drops of the compositions disclosed herein topically to the eye or eyes of the mammal or human. Determination of the number of drops administered per day to the person or mammal to provide effective relief is within the skill of the ordinary artisan.

In one embodiment, the composition is administered from 1 to 4 times per day.

In another embodiment, the composition is administered twice a day.

In another embodiment, the composition is administered only once a day.

In another embodiment, less than 14% of patients suffer ocular burning when the composition is administered only once a day for a period of three months.

In another embodiment, less than 10% of patients suffer ocular burning when the composition is administered only once a day for a period of three months.

In another embodiment, less than 8% of patients suffer ocular burning when the composition is administered only once a day for a period of three months.

Compositions

The concentration of cyclosporin A is less than about 0.05%. This is intended to mean that the concentration is lower than the concentration in the commercially available 0.05% cyclosporin A emulsion known as Restasis®.

In another embodiment, the concentration of cyclosporin A is from about 0.02% (w/v) to about 0.04% (w/v).

A liquid which is ophthalmically acceptable is formulated such that it can be administered topically to the eye. The comfort should be maximized as much as possible, although sometimes formulation considerations (e.g. drug stability) may necessitate less than optimal comfort. In the case that comfort cannot be maximized, the liquid should be formulated such that the liquid is tolerable to the patient for topical ophthalmic use. Additionally, an ophthalmically acceptable liquid should either be packaged for single use, or contain a preservative to prevent contamination over multiple uses.

For ophthalmic application, solutions or medicaments are often prepared using a physiological saline solution as a major vehicle. Ophthalmic solutions are often maintained at a comfortable pH with an appropriate buffer system. The formulations may also contain conventional, pharmaceutically acceptable preservatives, stabilizers and surfactants.

Various buffers and means for adjusting pH may be used so long as the resulting preparation is ophthalmically acceptable. Accordingly, buffers include, but are not limited to, acetate buffers, citrate buffers, phosphate buffers and borate buffers. Acids or bases may be used to adjust the pH of these formulations as needed.

In another embodiment, the composition contains a preservative.

Another embodiment is a method of treating ocular rosacea comprising topically administering to a mammal a multi-use composition comprising cyclosporin A at a concentration of from about 0.0001% (w/v) to less than about 0.2% (w/v), and an effective amount of a preservative.

Preservatives that may be used in the pharmaceutical compositions disclosed herein include, but are not limited to, cationic preservatives such as

• • quaternary ammonium compounds including benzalkonium chloride, polyquad, and the like;
  • guanidine-based preservatives including PHMB, chlorhexidine, and the like;
    chlorobutanol;
    mercury preservatives such as thimerosal, phenylmercuric acetate and phenylmercuric nitrate; and
    oxidizing preservatives such as stabilized oxychloro complexes (e.g. Purite®).

In another embodiment, the composition contains a surfactant.

A surfactant may be used for assisting in dissolving an excipient or an active agent, dispersing a solid or liquid in a composition, enhancing wetting, modifying drop size, or a number of other purposes. Useful surfactants include, but are not limited to surfactants of the following classes: alcohols; amine oxides; block polymers; carboxylated alcohol or alkylphenol ethoxylates; carboxylic acids/fatty acids; ethoxylated alcohols; ethoxylated alkylphenols; ethoxylated aryl phenols; ethoxylated fatty acids; ethoxylated; fatty esters or oils (animal & veg.); fatty esters; fatty acid methyl ester ethoxylates; glycerol esters; glycol esters; lanolin-based derivatives; lecithin and lecithin derivatives; lignin and lignin derivatives; methyl esters; monoglycerides and derivatives; polyethylene glycols; polymeric surfactants; propoxylated & ethoxylated fatty acids, alcohols, or alkyl phenols; protein-based surfactants; sarcosine derivatives; sorbitan derivatives; sucrose and glucose esters and derivatives.

In particular, ethoxylate surfactants are useful.

An ethoxylate surfactants is one that comprises the moiety —O(CH₂CH₂O)_n—OH, wherein n is at least about 1.

In one embodiment n is from about 1 to about 10,000.

In another embodiment, n is from 1 to about 1000.

In another embodiment, n is from about 1 to about 500.

Some ethoxylates contain one ethoxylate moiety. In other words, there is a single ethoxylate chain on each molecule.

Examples of surfactants with one ethoxylate moiety, include, but are not limited to:

Ethoxylated alcohols wherein the alcohol has a single hydroxyl unit; alkylphenol ethoxylates; ethoxylated fatty acids; fatty acid methyl ester ethoxylates; polyethylene glycols; and the like.

Ethoxylates may comprise more than one ethoxylate moiety. In other words, there may be ethoxylate moieties attached to several different parts of the molecule. Examples include, but are not limited to: block polymers; ethoxylated oils; sorbitan derivatives; sucrose and glucose ethoxylates; and the like.

Block Polymers: These are polymers with the structure A-B-A′, wherein A and A′ are polyethylene chains of 1 or more ethylene units, and B is a polypropylene chain of one or more propylene units. Generally, but not necessarily, A and A′ are approximately the same length.

In one embodiment, A and A′ contain from about 2 to about 200 ethylene units.
In another embodiment, A and A′ contain from about 5 to about 100 ethylene units.
In another embodiment, A and A′ contain about 7 to about 15 ethylene units.
In another embodiment, A and A′ contain about 7, about 8, or about 12 ethylene units.
In another embodiment, B contains from about 25 to about 100 propylene units.
In another embodiment, B contains from about 30 to about 55 propylene units.
In another embodiment, B contains about 30, about 34, or about 54 propylene units.
In another embodiment, the molecular weight is from about 1000 to about 20000.
In another embodiment, the molecular weight is from about 2000 to about 10000.
In another embodiment, the molecular weight is about 2500, about 3000, about 3800, or about 8400.

These include but are not limited to:

Poloxalene: wherein A has about 12 ethylene oxide units, B has about 34 propylene oxide units, A′ has about 12 ethylene oxide units, and the average molecular weight is about 3000.
Poloxamer 182: wherein A has about 8 ethylene oxide units, B has about 30 propylene oxide units, A′ has about 8 ethylene oxide units, and the average molecular weight is about 2500
Poloxamer 188: wherein A has about 75 ethylene oxide units, B has about 30 propylene oxide units, A′ has about 75 ethylene oxide units, and the average molecular weight is about 8400.
Poloxamer 331: wherein A has about 7 ethylene oxide units, B has about 54 propylene oxide units, A′ has about 7 ethylene oxide units, and the average molecular weight is about 3800;

Ethoxylated Alcohols

These include but are not limited to:

Ethoxylates of linear alcohols having from about 6 to about 20 carbon atoms.
In one embodiment, the linear alcohol has from about 10 to about 16 carbon atoms.
In another embodiment, n is from about 1 to about 100.
In another embodiment, n is from about 1 to about 50.
In another embodiment, n is from about 5 to about 50 ethylene oxide units.
In another embodiment, n is from about 1 to about 20 ethylene oxide units.
In another embodiment, n is from about 30 to about 50 ethylene oxide units.

Ethoxylated Alkylphenols

These are alkylphenols that are ethoxylated, i.e. the phenolic OH is replaced with an ethoxylate moiety.

These include but are not limited to:

octylphenol ethoxylate, i.e. C₈H₁₇Ph(OCH₂CH₂O)_nH.
nonylphenol ethoxylate, i.e. C₉H₁₉Ph(OCH₂CH₂O)_nH.
alkyphenols of the above formula wherein n is from about 1 to about 100.
alkyphenols of the above formula wherein n is from about 1 to about 50.
alkyphenols of the above formula wherein n is from about 9 to about 15.

Octyl Phenol 1.5 Mole Ethoxylate (i.e. n is an average of about 1.5); Octyl Phenol 5 Mole Ethoxylate; Octyl Phenol 7 Mole Ethoxylate; Octyl Phenol 9 Mole Ethoxylate; Octyl Phenol 12 Mole Ethoxylate; Octyl Phenol 40 Mole Ethoxylate; Nonyl Phenol 1.5 Mole Ethoxylate; Nonyl Phenol 4 Mole Ethoxylate; Nonyl Phenol 6 Mole Ethoxylate; Nonyl Phenol 9 Mole Ethoxylate; Nonyl Phenol 10 Mole Ethoxylate; Nonyl Phenol 10.5 Mole Ethoxylate; Nonyl Phenol 12 Mole Ethoxylate; Nonyl Phenol 15 Mole Ethoxylate; Nonyl Phenol 15 Mole Ethoxylate; Nonyl Phenol 30 Mole Ethoxylate; and Nonyl Phenol 40 Mole Ethoxylate;

Ethoxylated Fatty Acids,

These include but are not limited to:

ethoxylates which are esterified to form either:

• • monoesters, i.e. RCO₂(CH₂CH₂O)_nOH, where RCO₂H is a fatty acid; or
  • diesters, i.e. RCO₂(CH₂CH₂O)_nC(═O)R.

Fatty acids include, but are not limited to:

Saturated fatty acids, which have no C═C moieties and include myristic acid, palmitic acid, stearic acid, arachidic acid, behenic acid, lignoceric acid.
Unsaturated fatty acids, including the following:

• • monounsaturated fatty acids, which have one C═C group such as palmitoleic acid, oleic acid, and nervonic acid;
  • diunsaturated fatty acids, which have two C═C groups, such as linoleic acid;
  • triiunsaturated fatty acids, which have three C═C groups, such as α-linolenic acid and γ-linolenic acid;
  • tetraunsaturated fatty acids, which have four C═C groups, such as arachidonic acid; and
  • pentaunsaturated fatty acids, which have five C═C groups, such as eicosapentaenoic acid.

The following may also be used:

Lauric Acid; 14 carbon fatty acids such as myristic acid; 16 carbon fatty acids such as palmitic and palmitoleic acid; 18 carbon fatty acids such as stearic acid, oleic acid, linoleic acid, α-linolenic acid, and γ-linolenic acid; 20 carbon fatty acids such as eicosapentaenoic acid; 22 carbon fatty acids such as arachidic acid; and 24 carbon carbon fatty acids such as lignoceric acid and nervonic acid.

In one embodiment, n is from about 2 to about 100.

In another embodiment, n is from about 5 to about 50.

In another embodiment, n is from about 30 to 50.

Ethoxylated Fatty Esters or Oils (Animal & Veg.).

These are the products which result from reacting ethylene oxide with a fatty ester or an oil. When a fatty oil is used, the products is a mixture of ethoxylates of the fatty acids present in the oil, ethoxylates of glycerine, ethoxylates of mono and diglycerides, and the like.

Specific examples include, but are not limited to:

Ethoxylates of the following oils: Anise oil, Castor oil, Clove oil, Cassia oil, Cinnamon oil; Almond oil, Corn oil, Arachis oil, Cottonseed oil, Safflower oil, Maize oil, Linseed oil, Rapeseed oil, Soybean oil, Olive oil, Caraway oil, Rosemary oil, Peanut oil, Peppermint oil, Sunflower oil, Eucalyptus oil and Sesame oil; Coriander oil, Lavender oil, Citronella oil, Juniper oil, Lemon oil, Orange oil, Clary sage oil, Nutmeg oil, Tea tree oil, coconut oil, tallow oil, and lard;
In one embodiment, from 1 to about 50 moles of ethylene oxide is used per mole of the oil triglyceride.
In another embodiment, from about 30 to about 40 moles of ethylene oxide is used per mole of the oil triglyceride.

Ethylene oxide may also react with a fatty acid ester with a formula RCO₂R′ to form RCO₂(CH₂CH₂O)_nR′. Thus, surfactants having the formula RCO₂(CH₂CH₂O)_nR′, where RCO₂H is a fatty acid and R′ is alkyl having from 1 to 6 carbons are contemplated.

One embodiment is a fatty acid methyl ester ethoxylate, wherein R′ is methyl.

In another embodiment, RCO₂H is Lauric Acid; a 14 carbon fatty acid such as myristic acid; a 16 carbon fatty acid such as palmitic and palmitoleic acid; an 18 carbon fatty acids such as stearic acid, oleic acid, linoleic acid, α-linolenic acid, and γ-linolenic acid; a 20 carbon fatty acids such as eicosapentaenoic acid; a 22 carbon fatty acids such as arachidic acid; or a 24 carbon carbon fatty acids such as lignoceric acid and nervonic acid.

Polyethylene Glycols are ethoxylates that are unsubstituted, or terminated with oxygen on both ends, i.e. HO(CH₂CH₂O)_nH,

Sorbitan Derivatives:

These are ethoxylated sorbates having a fatty acid capping one or more of the ethoxylated chains. For example, polysorbate 80 has an oleate cap as shown in the structure below.

These compounds are named as POE (w+x+y+z) sorbitan mono (or di- or tri-) fatty acid.

For example, Polysorbate 80 is POE (20) sorbitan monooleate. Thus, the number in parenthesis is the total number of ethylene oxide units on the molecule, and the ending is the number of acid caps and the capping acid.

These include but are not limited to:

Sorbitan derivatives wherein the total number of ethylene oxide units is from 3 to 30;
Sorbitan derivatives wherein the total number of ethylene oxide units is 4, 5, or 20;
Sorbitan derivatives wherein the capping acid is laurate, palmitate, stearate, or oleate;
The sorbitan derivative may be a POE sorbitan monolaurate;
a POE sorbitan dilaurate;
a POE sorbitan trilaurate;
a POE sorbitan monopalmitate;
a POE sorbitan dipalmitate;
a POE sorbitan tripalmitate;
a POE sorbitan monostearate;
a POE sorbitan distearate;
a POE sorbitan tristearate;
a POE sorbitan monooleate;
a POE sorbitan dioleate;
or a POE sorbitan trioleate;

Specific examples include:

POE (20) sorbitan monolaurate; POE (4) sorbitan monolaurate; POE (20) sorbitan monopalmitate; POE (20) monostearate; POE (20) sorbitan monostearate; POE (4) sorbitan monostearate; POE (20) sorbitan tristearate; POE (20) sorbitan monoleate; POE (20) sorbitan 15 monoleate; POE (5) sorbitan 10 monoleate; POE (20) sorbitan trioleate; and

Sucrose and Glucose Esters and Derivatives:

Although there are a number of sucrose and glucose based surfactants, some sucrose and glucose esters and derivatives are similar to the sorbate derivatives described above. In other words, one, several, or all of the hydroxyl moieties of the sugar are ethoxylated, and one or more of the ethoxylate chains are capped with a carboxylic acid. Other sucrose and glucose esters are simply ethoxylated, but do not have a capping carboxylic acid. Other sucrose and glucose esters may be ethoxylated and capped with an alkyl group formed by reaction with an alcohol. Other sucrose and glucose esters may be esters or ethers of the sugars with hydrophobic chains and have ethoxylates substituted in other positions on the sugar.

Various useful vehicles may be used in the ophthalmic preparations disclosed herein. These vehicles include, but are not limited to, polyvinyl alcohol, povidone, hydroxypropyl methyl cellulose, poloxamers, carboxymethyl cellulose, hydroxyethyl cellulose, and acrylates (e.g. Pemulen®).

Tonicity adjustors may be added as needed or convenient. They include, but are not limited to, salts, particularly sodium chloride, potassium chloride, mannitol and glycerin, or any other suitable ophthalmically acceptable tonicity adjustor.

In a similar vein, an ophthalmically acceptable antioxidant includes, but is not limited to, sodium metabisulfite, sodium thiosulfate, acetylcysteine, butylated hydroxyanisole and butylated hydroxytoluene.

Other excipient components which may be included in the ophthalmic preparations are chelating agents. A useful chelating agent is edetate disodium, although other chelating agents may also be used in place or in conjunction with it.

Compositions may be aqueous solutions or emulsions, or some other acceptable liquid form. For an emulsion, one or more oils will be used to form the emulsion, and in some instances one or more surfactants will be required. Suitable oils include, but are not limited to anise oil, castor oil, clove oil, cassia oil, cinnamon oil, almond oil, corn oil, arachis oil, cottonseed oil, safflower oil, maize oil, linseed oil, rapeseed oil, soybean oil, olive oil, caraway oil, rosemary oil, peanut oil, peppermint oil, sunflower oil, eucalyptus oil, sesame oil, and the like.

In one embodiment, the composition is an aqueous solution.

In another embodiment, the composition contains no ethanol.

In another embodiment, the composition contains no hyaluronic acid.

In another embodiment, the composition contains no cyclodextrin A.

In another embodiment, the composition contains no cyclodextrin.

EXAMPLE 1

	Percent
	Ingredients	Amount needed (g)
Ingredients	(% w/v)	for a 1 liter batch
Cyclosporine	0% for Placebo	0 grams for Placebo
	(P)	(P)
	0.03% (A)	0.30 (A)
	0.04% (B)	0.40 (B)
	0.05% (C)	0.5 (C)
Carboxymethylcellulose	0.5	5.0
sodium
Polysorbate 80	1.0	10.0
Glycerin	1.0	10.0
Mannitol	0.5	5.0
Sodium Citrate	0.4	4.0
Dihydrate
Boric Acid	0.25	2.5
Sodium Borate	0.41	4.1
Decahydrate
Potassium Chloride	0.14	1.4
Purite	0.01	0.1
Purified Water	q.s. to 100%	q.s to 100%

Compositions P, A, B and C, are prepared according to the following procedure.

1. Measure Purified Water to about 90% of the batch size and place in an appropriate beaker or container.
2. Begin mixing the water with a strong mixer (Rotosolver) to obtain a strong vortex.
3. Add the pre-weighed carboxymethylcellulose sodium into the strong vortex. Continue strong mixing for at least 1 hour.
4. Slow mixer to a slow speed.
5. Add and dissolve the pre-weighed polysorbate 80.
6. Add and dissolve the pre-weighed glycerin.
7. Add and dissolve the pre-weighed mannitol.
8. Add and dissolve the pre-weighed sodium citrate dehydrate.
9. Add and dissolve the pre-weighed boric acid.
10. Add and dissolve the pre-weighed sodium borate decahydrate.
11. Add and dissolve the pre-weighed potassium chloride.
12. Check pH and adjust if necessary. Target pH is 7.5+/−0.1.
13. Add and dissolve the pre-weighed Purite.
14. Add sufficient quantity of Purified Water to attain the final batch volume. This will provide the finished placebo formulation (P).

Procedure for Either 0.03% (A), 0.04% (B), 0.05% (C)

15. Measure the exact amount of Placebo (9815X) needed to satisfy the batch size requirements and place in a media bottle that contains a magnetic stir bar.
16. Add and dissolve the pre-weighed cyclosporine. Stir at a slow speed to avoid foaming. It will usually take overnight mixing to completely dissolve the cyclosporine.
17. After overnight mixing is completed, pump the cyclosporine solution through a Millipore Milligard pre-filter and a Pall Suporlife sterilizing filter and collect the filtrate aseptically.
18. The sterile filtrate can then be aseptically dispensed into multidose dropper bottles suitable for ophthalmic purpose.
19. The finished product should be tested for cyclosporine assay, pH, osmolality, viscosity, Purite, sterility, and antimicrobial effectiveness.
20. The finished product should be store at room temperature and protected from light.

EXAMPLE 2

The following formulations were prepared. D and E were prepared by standard methods known in the art. F was prepared as described above for A-C except that Pemulen TR-2 was substituted for carboxymethylcellulose sodium, and the addition of the citrate and borate buffers were omitted.

	D	E	F
	Emulsion	Emulsion	Solution
	Cyclosporin A	0.05	0.05	0.05
	Castor Oil	1.25	0.30	N/A
	Polyoxyethylene	N/A	0.30	N/A
	40 Stearate, NF
	Polysorbate 80	1.00	0.30	1.00
	Glycerin	2.20	1.00	1.00
	Mannitol	N/A	2.00	2.00
	Pemulen TR-2	0.05	0.10	0.10
	Sodium Hydroxide	pH	pH	pH
	(1N)	adjustment	adjustment	adjustment
	Purified Water	QS	QS	QS
	pH	pH = 7.4	7.39	7.35

Bioavailability

The compositions disclosed and used herein provide a therapeutically effective amount of cyclosporin A to a mammal. However, while not intending to limit the scope of the invention in any way, concentrations of cyclosporin A in the compositions may be significantly lower than those normally associated with a therapeutically effective concentration. For example, one commercial preparation, marketed as Restasis® by Allergan, Inc., is a 0.05% cyclosporin A castor oil emulsion. Other compositions currently in development have concentrations of 0.1% or higher.

Reported herein are pharmacokinetic data for in vivo experiments on rabbits. However, the rabbit experiments are believed to be useful models for bioavailability in other mammals including humans. Thus, although bioavailability parameters are disclosed and featured in the claims, they should not be construed as limiting the treatment to rabbits only, but the compositions characterized and defined by bioavailability in rabbits are also contemplated for use in treatment in other mammals, particularly humans.

In one embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition A.

In another embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition B.

In another embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition C.

In one embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition D.

In another embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition E.

In another embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition F.

In one embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition G.

In another embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition H.

In another embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition I.

In another embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition J.

In another embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition K.

In another embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition L.

In another embodiment, the composition provides more cyclosporin A to the cornea of a person than Composition M.

In one embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition A.

In another embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition B.

In another embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition C.

In one embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition D.

In another embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition E.

In another embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition F.

In one embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition G.

In another embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition H.

In another embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition I.

In another embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition J.

In another embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition K.

In another embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition L.

In another embodiment, the composition provides more cyclosporin A to the conjunctiva of a person than Composition M.

In another embodiment, topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 500 ng of cyclosporin A per gram of cornea of said rabbit at 30 minutes after said topical administration.

In another embodiment, wherein topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 1000 ng of cyclosporin A per gram of cornea of said rabbit at 30 minutes after said topical administration.

In another embodiment, topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 1400 ng of cyclosporin A per gram of cornea of said rabbit at 30 minutes after said topical administration.

In another embodiment, wherein topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 2000 ng of cyclosporin A per gram of cornea of said rabbit at 30 minutes after said topical administration.

In another embodiment, topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 2400 ng of cyclosporin A per gram of cornea of said rabbit at 30 minutes after said topical administration.

In another embodiment, topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 17000 ng of cyclosporin A per gram of cornea of said rabbit over a period of 24 hours after said topical administration.

In another embodiment, said composition is an aqueous solution containing from 0.005% to about 0.04% cyclosporin A, wherein topical administration of one 35 μL drop of said composition to each eye of a New Zealand rabbit provides at least about 17000 ng of cyclosporin A per gram of cornea to the corneas of said rabbit as determined by:

• • topically administering said composition to each eye of each of 15 female New Zealand white rabbit test subjects; and determining the amount of cyclosporin A in the corneas of three subjects at times of about 0.5 hours, about 2 hours, about 6 hours, about 12 hours, and about 24 after administration to said subject;
    wherein the amount of cyclosporin A in the cornea is determined only once for each subject.

In another embodiment said composition to each eye of a New Zealand rabbit provides at least about 30000 ng of cyclosporin A per gram of cornea to the corneas of said rabbit.

In another embodiment said composition to each eye of a New Zealand rabbit provides at least about 45000 ng of cyclosporin A per gram of cornea to the corneas of said rabbit.

In another embodiment said composition to each eye of a New Zealand rabbit provides at least about 95000 ng of cyclosporin A per gram of cornea to the corneas of said rabbit.

In another embodiment said composition to each eye of a New Zealand rabbit provides at least about 155000 ng of cyclosporin A per gram of cornea to the corneas of said rabbit.

In another embodiment, topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the conjunctivas of said rabbit at least about 6000 ng of cyclosporin A per gram of conjunctiva of said rabbit over a period of 24 hours after said topical administration.

In another embodiment, said composition is an aqueous solution containing from 0.005% to about 0.04% cyclosporin A, wherein topical administration of one 35 μL drop of said composition to each eye of a New Zealand rabbit provides at least about 6000 ng of cyclosporin A per gram of conjunctiva to the conjunctivas of said rabbit as determined by:

• • topically administering said composition to each eye of each of 15 female New Zealand white rabbit test subjects; and determining the amount of cyclosporin A in the conjunctivas of three subjects at times of about 0.5 hours, about 2 hours, about 6 hours, about 12 hours, and about 24 after administration to said subject;
    wherein the amount of cyclosporin A in the conjunctiva is determined only a single time for each subject.

In another embodiment said composition to each eye of a New Zealand rabbit provides at least about 5000 ng of cyclosporin A per gram of conjunctiva to the conjunctiva of said rabbit.

In another embodiment said composition to each eye of a New Zealand rabbit provides at least about 7000 ng of cyclosporin A per gram of conjunctiva to the conjunctiva of said rabbit.

In another embodiment said composition to each eye of a New Zealand rabbit provides at least about 10000 ng of cyclosporin A per gram of conjunctiva to the conjunctiva of said rabbit.

In another embodiment said composition to each eye of a New Zealand rabbit provides at least about 17000 ng of cyclosporin A per gram of conjunctiva to the conjunctiva of said rabbit.

In another embodiment, the blood level of cyclosporin A is less than 0.1 mg/mL for a person for whom the composition has been administered twice a day topically to both eyes in 35 microliter drops for twelve months.

Pharmacokinetic Study

A 35 μL aliquot of one of three test formulations was topically administered to each eye of a female New Zealand White rabbit (n=3 rabbits/time point). At 0.5, 2, 6, 12, 24, 48 and 144 hours post-dose, cornea, conjunctiva, sclera, eyelid margin, nasolacrimal duct, and blood samples were collected. Samples collected from naïve rabbits (n=2) served as pre-dose samples. The quantitation ranges were 0.2-40 ng/mL in blood, 0.1-200 ng in cornea and conjunctiva, 0.1-100 ng in eyelid margin and nasolacrimal duct, and 0.1-20 ng in sclera and lacrimal gland.

The pharmacokinetic parameters of cyclosporine A in ocular tissues following a single ophthalmic instillation of one of three 0.05% cyclosporine A formulations are summarized in Table 1 below:

	TABLE 1
	Composition F	Composition E	Compositon D
	Cmax	AUC0-t	t1/2	Cmax	AUC0-t	t1/2	Cmax	AUC0-t	t1/2
Tissue/Matrix	(ng/g)	(ng · hr/g)	(hr)	(ng/g)	(ng · hr/g)	(hr)	(ng/g)	(ng · hr/g)	(hr)
Cornea	4050	163000	41.3	1100	76200	41.7	536	29300	49.8
Conjunctiva	4460	18100	11.3	2560	11600	5.57	694	5290	4.55
Sclera	545	6110	29.7	136	2840	24.8	53.0	1040	18.7
Eyelid Margin	3120	38300	42.5	2020	42200	38.1	2450	27700	24.4
Nasolacrimal	195	2190	NC	74.4	1190	NC	72.0	279	NC
Duct
Blood	2.21	NC	NC	0.441	NC	NC	BLQ	BLQ	NC
NC = Not calculable
BLQ = Below the limit of quantitation

Briefly summarizing, following a single ocular instillation of a 0.05% cyclosporine A formulation, the highest cyclosporine A ocular tissue exposure levels were observed from Composition F, followed by the Composition E, followed by Composition D.

Materials

Test Articles

Compositions D, E, and F, as described above, were used for these experiments.

Chemicals, Reagents and Supplies

All other chemicals were reagent grade or better.

Animals

Species, Strain, Sex, Age, Size, Source, and Identification

Female New Zealand White rabbits weighing 1.8 to 2.6 kg were purchased from Charles River (St. Constant, Quebec, Canada). A permanent ear tag was used to identify animals.

Justification

Similarities between the ocular anatomies of rabbits and humans make the rabbit an attractive animal model.

Animal Husbandry

All animals were housed in environmentally-controlled facility with a time-controlled fluorescent lighting system providing a daily 12-hour light/12-hour dark period. Room temperature was maintained between 61 and 72° F., and relative humidity between 30 and 70%. Airflow ranged from 10 to 30 air changes per hour. Temperature, humidity, and airflow were monitored by the Edstrom Watchdog system version 4.0.

The animals were provided Certified Hi-Fiber Rabbit Diet. Diet certification and analysis were provided by the vendor. No analysis outside those provided by the manufacturer was performed. Drinking water that was purified by a reverse osmosis process was offered ad libitum. Water was periodically analyzed for any contaminants that may interfere with the conduct of this study.

The manufacturer conducted analysis of animal feed.

Animal Acclimation

During the acclimatization period at Allergan, animals were kept under daily observation for any change in general health or behavior. Rabbits were quarantined for at least five days prior to the start of the study. All animals appeared healthy prior to and for the duration of the study.

Animal Termination and Disposal

Animals were euthanized via injection of at least 1 mL of sodium pentobarbital into a marginal ear vein.

Study Design and Experimental Procedures

Study Design

TABLE 1
Study design
Animal species and Rabbit, New Zealand White
strain
Gender             Female
Number             3 rabbits/time point
                   2 rabbits at pre-dose (bioanalytical
                   controls)
Body Weights       1.8-2.8 kg
Dosing Regimen     Topical ocular, single dose, bilateral
Dose Volume        35 μL
Test Article       Formulations containing 0.05% AGN
                   192371 (cyclosporine A)
Time Points        0.5, 2, 6, 12, 24, 48, and 144 hours
                   post-dose
Tissues/Matrices   Cornea, conjunctiva, sclera,
                   nasolacrimal duct, eyelid margin and
                   blood
Assay Method       LC-MS/MS
Analyte            AGN 192371 (Cyclosporine A)
Quantitation Range Blood: 0.5-40 ng/mL
                   Cornea: 0.1-200 ng
                   Conjunctiva: 0.1-200 ng
                   Eyelid Margin: 0.1-100 ng
                   Nasolacrimal Duct: 0.1-100 ng
                   Sclera:: 0.1-20 ng

Single bilateral dose, 3 rabbits (6 eyes and 3 blood samples) per time point. Two animals in group 4 were not dosed and were used as bioanalytical controls. Prior to dosing, 65 animals were weighed and assigned to 4 study groups. The study design is presented in Table 1. The four study groups are presented in the Table 2 below:

TABLE 2
		Dose
Group	Treatment	(μL)	Frequency	n
1	Composition F	35	Single Bilateral	3F per time
			Dose	point
				(total of 21F)
2	Composition E	35	Single Bilateral	3F per time
			Dose	point
				(total of 21F)
3	Composition D	35	Single Bilateral	3F per time
			Dose	point
				(total of 21F)
4	No Dose	—	—	2F
				(total of 2F)
n = Number of animals per group
F = Female

Pretreatment Examinations

Prior to placement on study, a physical examination was performed on each animal. Gross observations were recorded prior to drug administration and immediately after ocular dose using a standardized data collection sheet.

Randomization

Prior to dosing, 65 animals were weighed and randomly assigned to four study groups.

Dosing Procedure:

Animals were dosed once by ocular instillation bilaterally at Hour 0 of the study. Immediately prior to dosing, the eye was inspected for any abnormalities, such as infection, red eye, or visible damage. Only animals without visible abnormalities were used. The lower eyelid was gently pulled out and away from the eye. Using a Gilson precision pipette, 35 μL of dosing solution was instilled into the lower cul-de-sac of each eye. The time of dose administration was recorded. The eye was gently held closed for approximately 5 seconds to ensure even dose distribution around the eye. Gross ocular observations were performed following dosing. The animal, including the dosed eyes, were subjectively evaluated for signs of irritation. Observations were recorded.

Mortality/Morbidity

Animals were observed for mortality/morbidity during the study.

Body Weights

Animals were weighed the day before dose administration and subsequently randomized.

Pre-necropsy Blood Collection

Blood was collected from each rabbit prior to euthanasia/necropsy. Animals were anesthetized with an intravenous injection of a ketamine/xylazine cocktail (87 mg/mL ketamine, 13 mg/mL xylazine) at a volume of 0.1 mL/kg. Blood was collected via cardiac puncture. Approximately 5 mL of blood was collected into 10 mL lavender top (K₃EDTA) tubes. Blood samples were stored at or below approximately −15° C. until bioanalysis.

Euthanasia

Animals were euthanized with an intravenous injection of commercial euthanasia solution following blood collection.

Necropsy and Collection of Ocular Tissues

Ocular samples were collected from both eyes, blotted dry where applicable, weighed and placed in separate, appropriately labeled, silanized vials, at the time of necropsy. Both eyes were rinsed with LENS PLUS® in order to clear residual surface formulation remaining on the ocular surface.

Conjunctiva

The upper and lower conjunctiva from each eye were removed and pooled, weight recorded, placed into separate screw-cap glass 13×100 silanized test tubes and immediately placed on ice. Samples were stored at or below −15° C. until bioanalysis.

Cornea

The entire cornea was removed from each eye; weight recorded, placed into separate screw-cap glass 13×100 silanized test tubes and immediately placed on ice. Samples were stored at or below −15° C. until bioanalysis.

Sclera

The sclera was removed from each eye; weight recorded, placed into separate screw-cap glass 13×100 silanized test tubes and immediately placed on ice. Samples were stored at or below −15° C. until bioanalysis.

Nasolacrimal Duct

Tissue containing the nasolacrimal duct associated with each eye was removed; weight recorded, placed into screw-cap glass 13×100 silanized test tubes and immediately placed on ice. Samples were stored at or below −15° C. until bioanalysis.

Eyelid Margin

The eyelid margins were removed from each eye; weight recorded, placed into separate screw-cap glass 13×100 silanized test tubes and immediately placed on ice. Samples were stored at or below −15° C. until bioanalysis.

Sample Storage

Blood and ocular tissue samples were stored at or below −15° C. until bioanalysis.

Bioanalysis

Ocular tissue and blood concentrations were quantified using the following method.

Ocular tissue samples were extracted by soaking over night with 2.0 mL methanol at 4° C. This was followed by a second soak with 2.0 mL methanol and shaking for approximately one hour at room temperature. An aliquot of 1 mL from a total of 4 mL organic extract was removed (all 4 mL were analyzed for lacrimal gland samples), and internal standard added (20 μL of 500 ng/mL of CsG). The methanolic extract was evaporated to dryness and reconstituted with 200 μL of 2 mM ammonium acetate/0.4% formic acid in 50:50 acetonitrile:water for LC MS/MS analysis. The bioanalytical procedure for analysis of blood samples involved addition of internal standard, CsG (10 μL of 500 ng/mL) to 0.5 mL aliquots of K3EDTA-treated rabbit blood.

Following incubation of blood sample for 30 minutes at 37° C., the samples were acidified with 0.1 N HCL (2 mL). Methyl t-butyl ether (4 mL) was added to each sample and mixed for 15 minutes. The organic layer was removed and made basic by addition of 0.1 N NaOH (2 mL). The organic extract was separated from the aqueous layer, evaporated to dryness and reconstituted with 200 μL of 2 mM ammonium acetate/0.4% formic acid in 50:50 acetonitrile:water for LC MS/MS analysis. Aliquots (50 μL) of the reconstituted samples were analyzed by LC-MS/MS using a PE Sciex API 3000 mass spectrometer (Applied Biosystems, Foster City, Calif.), Leap autosampler (Carrboro, N.C.), and HPLC pumps (Shimadzu Scientific Instruments, Columbia, Md.). Reverse-phase HPLC was performed on a Keystone BDS C8 column (3 μm, 2.1×50 mm, 65° C.) with solvent gradient elution (A=2 mM ammonium acetate/0.4% formic acid in water and B=2 mM ammonium acetate/0.4% formic acid in acetonitrile) at a flow rate of 0.3 mL/min. The precursor-product ion pairs used in MRM analysis were: 1203 (MH)⁺→425.5 for CsA and m/z 1217 (MH)⁺)→425.5 for IS(Cyclosporin G). The total analysis time was 5 min, with retention times of CsA and CsG at approximately 1.82 and 1.86 minutes, respectively.

Data Treatment

Data Collection

Pre and post treatment gross ocular examinations

Body Weights: Randomization at Day −1

Dosing Notes

Mortality/Morbidity

Blood Samples: Pre-necropsy

Ocular Tissue Samples: Post-necropsy

Data Calculation and Outlier Analysis

All data was used in calculations unless omitted for reasons justified in the raw data.

Pharmacokinetic Analysis

Thermo Electron Watson™ (Philadelphia, Pa.) and Microsoft®Excel (Redmond, Wash.) were used for pharmacokinetic calculations. The pharmacokinetic parameters listed below were calculated using a known non-compartmental approach (see Tang-Lui, et. al. Pharmaceutical Research, Vol 5, No. 4, 1988, 238-241). The pharmacokinetic data was described using descriptive statistics such as mean and standard deviation whenever possible. Area under the concentration-time profile (AUC) values were reported as a composite AUC and whenever possible, standard error of the mean (SEM).

PK Parameter    Description
Cmax (ng/mL) or Maximum observed concentration
(ng/g)
Tmax (hr)       Time corresponding to maximum observed
                concentration
AUC0-t          Area under concentration time curve from time zero
(ng · hr/g)     to the last quantifiable time point using the
                random method for non-sequential sampling
t1/2 (hr)       Half-life
MRT (hr)        Mean residence time

Values below the Limit of Quantitation and Number Rounding

If more than half of the concentration values contributing to a calculation of the mean were below limit of quantitation (BLQ), then the statistics were reported as non-calculable (NC). If half or more of the values were quantifiable, then any BLQ values were replaced with a value of “0”, and the mean and its standard deviation (SD) were calculated with these replaced values. The mean and standard deviation of the mean were calculated at each sampling time point within each treatment group. Whenever the sample size was less than or equal to 2, only mean values were listed. All mean values were reported to 3 significant figures and standard deviations were reported to the same decimal place as their respective mean values.

Protocol Deviations

Prior to collection of ocular tissue samples at the 6 hour time point, the eyes were not rinsed with Lens Plus® to clear any residual surface formulation remaining on the ocular surface. It is believed that this deviation will have minimal impact on the results derived from this study since in general this drug is rapidly absorbed from the ocular surface. In addition, blinking by the rabbits over 6 hours should also act to clear any residual surface formulation.

Abbreviations
ACN          Acetonitrile
ALQ          Above Limits of Quantitation
AUC          Area Under the Plasma or Blood Drug Concentration -
             Time Curve
AUCExtrap    Extrapolated Area Under the Plasma or Blood Drug
             Concentration Time Curve from Time 0 to the Last
             Quantifiable Timepoint
BID          Two Times Daily
BLQ          Below Limit of Quantitation
BMS          Bioanalytical Mass Spectrometry
CFR          Code of Federal Regulations
C0 or C0     Extrapolated Plasma or Blood Drug Concentrations at
             the Time 0
Cmax or Cmax Maximal Drug Concentration
CONC         Concentration
DG           Day of Gestation
DSE          Drug Safety Evaluation
EDTA (K3)    Potassium Ethylenediaminetetraacetic Acid
F            Female
GD           Gestation Day
FDA          United States Food and Drug Administration
GLP          Good Laboratory Practice
IC           Intracardiac
IS           Insufficient Sample Received
IM           Intramuscular
IU           International Units
IV           Intravenous
IVT          Intravitreal
LC-MS/MS     Liquid Chromatography Tandem Mass Spectrometry
LLOQ         Lower Limit of Quantitation
M            Male
N, n, No.,   Number
no.
N/A, N.A.,   Not Applicable
or n/a
N/C, N.C.,   Not Calculable
NC, or n/c
NR           No Result/Not Reported
NS           No Sample
NZW          New Zealand White
OD           Right Eye
OU           Both Eyes
PKDM         Pharmacokinetics and Drug Metabolism
PO           By Mouth
QID          Four Times Daily
QNS          Quantity Not Sufficient
SD, S.D.,    Standard Deviation
or sd
SE           Standard Error
Sec          Seconds
SMP          Sample
T½ or T1/2   Drug Half Life
TA           Triamcinolone Acetonide
TID          Three Times Daily
TK           Toxicokinetic
Tmax or Tmax Time at which Cmax is Observed
U            Units
ULOQ         Upper Limit of Quantitation
Note:
Not all abbreviations listed may appear in this report.

Results and Discussion

Cornea

The mean concentrations and pharmacokinetic parameters are summarized in Tables 3 and 4. The concentration-time profiles of cyclosporine A in cornea following a single bilateral ocular administration of one of three 0.05% cyclosporine A formulations to rabbits are presented in FIG. 1.

TABLE 3
Mean cornea concentrations of cyclosporine A following a single
bilateral topical ocular instillation of one of three 0.05% cyclosporine
A formulations to New Zealand White rabbits.
	Cyclosporine A concentration (ng/g)
Time	Composition F	Composition E	Composition D ®
(hr)	Mean	SD	Mean	SD	Mean	SD
0.5	4050	1220	1020	330	295	201
2	2740	620	1100	190	432	142
6	3030	750	1010	170	536	138
12	2530	430	858	267	417	127
24	1570a	390	891a	115	256a	28.2
48	1240a	230	622a	118	238a	76.6
144	222a	61	125a	47	52.5a	13.2
Mean values represent an average of n = 6
aConcentration time points used to calculate t1/2

TABLE 4
Pharmacokinetic parameters in cornea of cyclosporine A following
a single bilateral topical ocular instillation of one of three 0.05%
cyclosporine A formulations to New Zealand White rabbits.
Parameter	Composition F	Composition E	Composition D ®
Cmax (ng/g)	4050 ± 1220	1100 ± 190	536 ± 138
Tmax (hr)	0.500	2.00	6.00
AUC0-t	163000 ± 7000	76200 ± 3300	29300 ± 2000
(ng · hr/g) a
AUC0-24	59000	22100	9450
(ng · hr/g)
t1/2 (hr)	41.3	42.2	49.8
MRT (hr)	50.3	56.5	61.6
a An AUC interval of 0-144 hours was used for calculations for the three formulations

Composition F

Following a single bilateral ocular instillation of Composition F, cyclosporine A was rapidly absorbed into the cornea with a peak corneal concentration (C_max) of 4050±1220 ng/g, occurring 0.500 hours post-dose. The area under the concentration-time curve (AUC_0-t) value through the last quantifiable time point was 163000±7000 ng·hr/g and the AUC_0-24 value was 59000 ng·hr/g. The terminal half-life (t_1/2) was 41.3 hours and the mean residence time (MRT) was 50.3 hours.

Composition E

Following a single bilateral ocular instillation of Composition E, cyclosporine A was absorbed into the cornea with C_max value of 1100±190 ng/g, occurring 2.00 hours post-dose. The AUC_0-t value was 76200±3300 ng·hr/g and the AUC_0-24 value was 22100 ng·hr/g. The terminal t_1/2 was 41.7 hours and the MRT was 56.5 hours.

Composition D

Following a single bilateral ocular instillation of Composition D, cyclosporine A was absorbed into the cornea with a C_max value of 536±138 ng/g, occurring 6.00 hours post-dose. The AUC_0-t value was 29300±2000 ng·hr/g and the AUC_0-24 value was 9450 ng·hr/g. The terminal t_1/2 was 49.8 hours and the MRT was 61.6 hours.

Conjunctiva

The mean concentrations and pharmacokinetic parameters are summarized in Tables 5 and 6. The concentration-time profiles of cyclosporine A in conjunctiva following a single bilateral ocular administration of one of three 0.05% cyclosporine A formulations to rabbits are presented in FIG. 2.

TABLE 5
Mean conjunctiva concentrations of cyclosporine A following a
single bilateral topical ocular instillation of one of three 0.05%
cyclosporine A formulations to New Zealand White rabbits.
	Cyclosporine A concentration (ng/g)
Time	Composition F	Composition E	Composition D ®
(hr)	Mean	SD	Mean	SD	Mean	SD
0.5	4460	650	2560	1070	694	410
2	2170	530	1410	330	665	266
6	739	208	630a	197	330a	143
12	292a	97	178a	34	110a	52.3
24	58.2a	12.5	60.5a	32.5	20.5a	13.2
48	26.9a	19.1	BLQ	—	BLQ	—
144	BLQ	—	BLQ	—	BLQ	—
Mean values represent an average of n = 6
BLQ = Below the limit of quantitation
aConcentration time points used to calculate t1/2

TABLE 6
Pharmacokinetic parameters in conjunctiva of cyclosporine A following
a single bilateral topical ocular instillation of one of three 0.05%
cyclosporine A formulations to New Zealand White rabbits.
Parameter	Composition F	Composition E	Composition D ®
Cmax (ng/g)	4460 ± 650	2560 ± 1070	694 ± 410
Tmax (hr)	0.500	0.500	0.500
AUC0-t	18100 ± 800a	11600 ± 700b	5290 ± 480b
(ng · hr/g)
AUC0-24	17100	11600	5290
(ng · hr/g)
t1/2 (hr)	11.3	5.57	4.55
MRT (hr)	7.37	5.93	6.07
aAn AUC interval of 0-48 hours was used for calculations
bAn AUC interval of 0-24 hours was used for calculations

Composition F

Following a single bilateral ocular instillation of Composition F, cyclosporine A was rapidly absorbed into the conjunctiva with a C_max value of 4460±650 ng/g, occurring 0.500 hours post-dose. The AUC_0-t value was 18100±800 ng·hr/g and the AUC_0-24 value was 17100 ng·hr/g. The terminal t_1/2 was 11.3 hours and the MRT was 7.37 hours.

Composition E

Following a single bilateral ocular instillation of Composition E, cyclosporine A was rapidly absorbed into the conjunctiva with a C_max value of 2560±1070 ng/g, occurring 0.500 hours post-dose. The AUC_0-t value was 11600±700 ng·hr/g. The terminal t_1/2 was 5.57 hours and the MRT was 5.93 hours.

Composition D

Following a single bilateral ocular instillation of Composition D, cyclosporine A was rapidly absorbed into the conjunctiva with a C_max value of 694±410 ng/g, occurring 0.500 hours post-dose. The AUC_0-t value was 5290±480 ng·hr/g. The terminal t_1/2 was 4.55 hours and the MRT was 6.07 hours.

Sclera

The mean concentrations and pharmacokinetic parameters are summarized in Tables 7 and 8. The concentration-time profiles of cyclosporine A in sclera following a single bilateral ocular administration of one of three 0.05% cyclosporine A formulations to rabbits are presented in FIG. 3.

TABLE 7
Mean sclera concentrations of cyclosporine A following a single
bilateral topical ocular instillation of one of three 0.05% cyclosporine
A formulations to New Zealand White rabbits.
	Cyclosporine A concentration (ng/g)
Time	Composition F	Composition E	Composition D ®
(hr)	Mean	SD	Mean	SD	Mean	SD
0.5	545	98	136	44	52.5	29.3
2	294	74	120	34	49.4	24.5
6	210	58	83.7	14.0	53.0	10.9
12	133	25	51.0	19.1	28.6a	3.7
24	51.4a	9.4	36.5a	9.9	13.5a	2.3
48	24.2a	7.1	13.0a	3.61	7.10a	3.09
144	2.92a	0.40	1.14a	1.27	BLQ	—
Mean values represent an average of n = 6
BLQ = Below the limit of quantitation
aConcentration time points used to calculate t1/2

TABLE 8
Pharmacokinetic parameters in sclera of cyclosporine A following
a single bilateral topical ocular instillation of one of three 0.05%
cyclosporine A formulations to New Zealand White rabbits.
Parameter	Composition F	Composition E	Composition D ®
Cmax (ng/g)	545 ± 98	136 ± 43	53.0 ± 10.9
Tmax (hr)	0.500	0.500	6.00
AUC0-t	6110 ± 260a	2840 ± 150a	1040 ± 50b
(ng · hr/g)
AUC0-24	3900	1560	792
(ng · hr/g)
t1/2 (hr)	29.7	24.8	18.7
MRT (hr)	25.3	26.9	23.8
aAn AUC interval of 0-144 hours was used for calculations
bAn AUC interval of 0-48 hours was used for calculations

Composition F

Following a single bilateral ocular instillation of Composition F, cyclosporine A was rapidly absorbed into the sclera with a C_max value of 545±98 ng/g, occurring 0.500 hours post-dose. The AUC_0-t value was 6110±260 ng·hr/g and the AUC_0-24 value was 3900 ng·hr/g. The terminal t_1/2 was 29.7 hours and the MRT was 25.3 hours.

Composition E

Following a single bilateral ocular instillation of Composition E, cyclosporine A was rapidly absorbed into the sclera with a C_max value of 136±43 ng/g, occurring 0.500 hours post-dose. The AUC_0-t value was 2840±150 ng·hr/g and the AUC_0-24 value was 1560 ng·hr/g. The terminal t_1/2 was 24.8 hours and the MRT was 26.7 hours.

Composition D

Following a single bilateral ocular instillation of Composition D®, cyclosporine A was absorbed into the sclera with a C_max value of 53.0±10.9 ng/g, occurring 6.00 hours post-dose. The AUC_0-t value was 1040±50 ng·hr/g and the AUC_0-24 value was 792 ng·hr/g. The terminal t_1/2 was 18.7 hours and the MRT was 23.8 hours.

Eyelid Margin

The mean concentrations and pharmacokinetic parameters are summarized in Tables 9 and 10. The concentration-time profiles of cyclosporine A in the eyelid margin following a single bilateral ocular administration of one of three 0.05% cyclosporine A formulations to rabbits are presented in FIG. 4.

TABLE 9
Mean eyelid margin concentrations of cyclosporine A following a
single bilateral topical ocular instillation of one of three 0.05%
cyclosporine A formulations to New Zealand White rabbits.
	Cyclosporine A concentration (ng/g)
Time	Composition F	Composition E	Composition D ®
(hr)	Mean	SD	Mean	SD	Mean	SD
0.5	3120	1040	2020	980	1800	900
2	1710	300	1380	630	2450	970
6	679	135	547	300	430	214
12	787	280	910	199	662	506
24	263a	158	138a	87	222a	172
48	223a	207	362a	437	112a	82
144	40.0a	22.5	24.9a	23.4	7.30a	12.64
Mean values represent an average of n = 6
aConcentration time points used to calculate t1/2

TABLE 10
Pharmacokinetic parameters in eyelid margin of cyclosporine A following
a single bilateral topical ocular instillation of one of three 0.05%
cyclosporine A formulations to New Zealand White rabbits.
Parameter	Composition F	Composition E	Composition D ®
Cmax (ng/g)	3120 ± 1040	2020 ± 980	2450 ± 970
Tmax (hr)	0.500	0.500	2.00
AUC0-t	38300 ± 5300	42200 ± 10800	27700 ± 3300
(ng · hr/g)a
AUC0-24	19900	17600	18000
(ng · hr/g)
t1/2 (hr)	42.5	38.2	24.4
MRT (hr)	40.5	38.4	21.9
aAn AUC interval of 0-144 hours was used for calculations for the three formulations

Composition F

Following a single bilateral ocular instillation of Composition F, cyclosporine A was rapidly absorbed into the eyelid margin with a C_max value of 3120±1040 ng/g, occurring 0.500 hours post-dose. The AUC_0-t value was 38300±5300 ng·hr/g and the AUC_0-24 value was 19900 ng·hr/g. The terminal t_1/2 was 42.5 hours and the MRT was 40.5 hours.

Composition E

Following a single bilateral ocular instillation of Composition E, cyclosporine A was rapidly absorbed into the eyelid margin with a C_max value of 2020±980 ng/g, occurring 0.500 hours post-dose. The AUC_0-t value was 42200±10800 ng·hr/g and the AUC_0-24 value was 17600 ng·hr/g. The terminal t_1/2 was 38.1 hours and the MRT was 38.4 hours.

Composition D

Following a single bilateral ocular instillation of Composition D, cyclosporine A was absorbed into the eyelid margin with a C_max value of 2450±970 ng/g, occurring 2.00 hours post-dose. The AUC_0-t value was 27700±3300 ng·hr/g and the AUC_0-24 value was 18000 ng·hr/g. The terminal t_1/2 was 24.4 hours and the MRT was 21.9 hours.

Nasolacrimal Duct

The mean concentrations and pharmacokinetic parameters are summarized in Tables 11 and 12. The concentration-time profiles of cyclosporine A in nasolacrimal duct tissue following a single bilateral ocular administration of one of three 0.05% cyclosporine A formulations to rabbits are presented in FIG. 5.

TABLE 11
Mean nasolacrimal duct concentrations of cyclosporine A following
a single bilateral topical ocular instillation of one of three 0.05%
cyclosporine A formulations to New Zealand White rabbits.
	Cyclosporine A concentration (ng/g)
Time	Composition F	Composition E	Composition D ®
(hr)	Mean	SD	Mean	SD	Mean	SD
0.5	194	201	74.4	20.9	72.0	91.7
2	43.7	44.1	37.2	43.6	37.4	13.8
6	18.2	15.2	BLQ	—	11.8	10.0
12	24.2	12.0	35.5	21.5	14.9	8.4
24	BLQ	—	BLQ	—	BLQ	—
48	BLQ	—	4.68	5.15	BLQ	—
144	1.71	1.93	BLQ	—	BLQ	—
Mean values represent an average of n = 6
BLQ = Below the limit of quantitation

TABLE 12
Pharmacokinetic parameters in nasolacrimal duct of
Cyclosporine A following a single bilateral topical
ocular instillation of one of three 0.05% cyclosporine
A formulations to New Zealand White rabbits.
Parameter	Composition F	Composition E	Composition D ®
Cmax (ng/g)	195 ± 201	74.4 ± 20.9	72.0 ± 91.7
Tmax (hr)	0.500	0.500	0.500
AUC0-t	2190 ± 350a	1190 ± 212b	279 ± 39c
(ng · hr/g)
AUC0-12	478 ± 86	465 ± 106	279 ± 39
(ng · hr/g)
t1/2 (hr)	NC	NC	NC
MRT (hr)d	17.6	24.7	12.1
NC = Not calculable
aAn AUC interval of 0-144 hours was used for calculations
bAn AUC interval of 0-48 hours was used for calculations
cAn AUC interval of 0-12 hours was used for calculations
dA time interval of 0-12 hours was used for calculations

Composition F

Following a single bilateral ocular instillation of Composition F, cyclosporine A rapidly drained into and was then absorbed into the nasolacrimal duct tissue with a C_max value of 195±201 ng/g, occurring 0.500 hours post-dose. The AUC_0-t value was 2190±350 ng·hr/g and the AUC_0-12 value was 478±86 ng·hr/g. The MRT was 17.6 hours.

Composition E

Following a single bilateral ocular instillation of Composition E, cyclosporine A rapidly drained into and was then absorbed into the nasolacrimal duct tissue with a C_max value of 74.4±20.9 ng/g, occurring 0.500 hours post-dose. The AUC_0-t value was 1190±210 ng·hr/g and the AUC_0-12 value was 465±106 ng·hr/g. The MRT was 24.7 hours.

Composition D

Following a single bilateral ocular instillation of Composition D, cyclosporine A rapidly drained into and was then absorbed into the nasolacrimal duct tissue with a C_max value of 72.0±91.7 ng/g, occurring 0.500 hours post-dose. The AUC_0-t value was 279±39 ng·hr/g. The MRT was 12.1 hours.

Blood

The mean concentrations of cyclosporine A in blood are summarized in Table 13.

TABLE 13
Mean blood concentrations of Cyclosporine A following a single
bilateral topical ocular instillation of one of three 0.05%
cyclosporine A formulations to New Zealand White rabbits.
	Cyclosporine A concentration (ng/mL)
Time	Composition F	Composition E	Composition D ®
(hr)	Mean	SD	Mean	SD	Mean	SD
0.5	2.21	0.33	0.441	0.126	BLQ	—
2	0.463	0.021	BLQ	—	BLQ	—
6	BLQ	—	BLQ	—	BLQ	—
12	BLQ	—	BLQ	—	BLQ	—
24	BLQ	—	BLQ	—	BLQ	—
48	BLQ	—	BLQ	—	BLQ	—
144	BLQ	—	BLQ	—	BLQ	—
Mean values represent an average of n = 3
BLQ = Below the limit of quantitation

Composition F

Following a single bilateral ocular instillation of Composition F, cyclosporine A was detected at 0.5 and 2 hours post-dose in the blood at concentrations of 2.21±0.33 ng/mL and 0.463±0.021 ng/mL, respectively. Cyclosporine A levels were below the limit of quantitation at all subsequent time points.

Composition E

Following a single bilateral ocular instillation of Composition E, cyclosporine A was detected at 0.5 hours post-dose in the blood at a concentration of 0.441±0.126 ng/mL. Cyclosporine A levels were below the limit of quantitation at all subsequent time points.

Composition D

Following a single bilateral ocular instillation of Composition D, cyclosporine A levels were below the limit of quantitation at all time points.

Administration of Composition F to rabbits generally delivered the highest levels of cyclosporine A to ocular tissues, on average a 5-fold increase in area under the concentration-time profile (AUC) was observed when compared to Composition D. Administration of Composition E to rabbits resulted on average in a 2-fold increase in AUC when compared to Composition D. The pharmacokinetic profile observed following Composition D administration to New Zealand White rabbits in this study was in good agreement with previously reported data.

In general, the terminal half-life and mean residence time observed were greatest for Composition F, followed by the Composition E, followed by Composition D. Thus, AUC values were reported to the last quantifiable time point, in addition to AUC through 24 hours for cornea, conjunctiva, sclera and eyelid margin and AUC through 12 hours for nasolacrimal duct to make an assessment over the same interval as to the drug levels achieved following once a day dosing. Overall, the trends observed when comparing AUC_0-t values were consistent with the trends observed when comparing AUC_0-24 or AUC_0-12.

In conclusion, following a single ocular instillation of a 0.05% cyclosporine A formulation, the highest cyclosporine A ocular tissue exposure levels were observed when drug was formulated as an aqueous Composition F, followed by the Composition E followed by Composition D. A concomitant trend was observed in blood drug exposure.

While not intending to limit the scope of the invention, it is believed that these pharmacokinetic results suggest that significantly lower concentrations of cyclosporin A may be used in topical ophthalmic compositions than previously known and still achieve a therapeutically effective amount cyclosporin A.

Standard Compositions

These compositions (A-M) are particularly contemplated for use as standards for comparison for characterization of the compositions disclosed herein. However, these compositions are also contemplated for use in treatment of ocular rosacea and the signs and symptoms associated therewith.

The following compositions are intended to mean those identical to those disclosed in Kanai et. al., Transplantation Proceedings, Vol 21, No 1 (February), 1989: 3150-3152, which is incorporated by reference herein:

• • Composition A: a solution consisting of 0.025% cyclosporin A, 40 mg/mL alpha cyclodextrin, and water;
  • Composition B: a solution consisting of 0.009% cyclosporin A, 20 mg/mL alpha cyclodextrin, and water; and
  • Composition C: a solution consisting of 0.003% cyclosporin A, 10 mg/mL alpha cyclodextrin, and water.

The following composition is intended to mean those identical to that disclosed in Cheeks et. al., Current Eye Research, Vol 11, No 7 (1992), 641-649, which is incorporated by reference herein:

• • Composition D: an alpha cyclodextrin solution at 40 mg/mL containing 0.025% cyclosporin A.

The following composition is intended to mean that identical that disclosed in Tamilvanan, Stp Pharma Sci November-December; 11(6):421-426, which is incorporated by reference herein, except that the concentration of cyclosporin A is different.

• • Composition E: an emulsion consisting of cyclosporin A (0.05 w/w %), castor oil (2.5 w/w %), stearylamine (0.12 w/w %), α-tocopherol (0.01 w/w %), benzalkonium chloride (0.01 w/w %) and water up to 100 w/w %.

The following compositions are intended to mean those identical to Samples C-E disclosed in U.S. Pat. No. 5,051,402 (column 7). The entire disclosure is incorporated herein by reference.

• • Composition F: 0.25 mL/mL of cyclosporin A, 40 mg/mL of α-cyclodextrin, and 7.79 mg/mL of sodium chloride;
  • Composition G: 0.10 mL/mL of cyclosporin A, 20 mg/mL of α-cyclodextrin, and 8.40 mg/mL of sodium chloride; and
  • Composition H: 0.05 mL/mL of cyclosporin A, 10 mg/mL of α-cyclodextrin, and 8.70 mg/mL of sodium chloride.

The following composition is intended to mean that identical that disclosed in Abdulrizak, Stp Pharma Sci November-December; 11(6):427-432, which is incorporated by reference herein, except that the concentration of cyclosporin A is different.

• • Composition I: an emulsion consisting of cyclosporin A (0.05 w/w %), castor oil (2.5 w/w %), Poloxamer 188, (0.425 w/w %), glycerol (2.25 w/w %), Lipoid E-80 (0.5 w/w %), stearylamine (0.12 w/w %), tocopherol (0.01 w/w %), benzalkonium chloride (0.01 w/w %), and water.

The following composition is intended to mean that identical to that disclosed in Kuwano Mitsuaki et al. Pharm Res 2002 Aug.; 19(1):108-111.

• • Composition J: a solution consisting of cyclosporine A (0.0865%), ethanol (0.1%), MYS-40 (2%), HPMC (0.3 w/v %), sodium dihydrogen phosphate (0.2 w/v %), and disodium EDTA (0.01% w/v %), sodium chloride to adjust the tonicity to 287 mOsm, and water.

Composition K is intended to mean that disclosed in US20010041671, incorporated by reference herein, as Formulation 1, on Table 1. Composition L is that disclosed in US20010041671 as Formulation 3, except that the concentration of cyclosporine is reduced.

• • Composition K: cyclosporine A (0.02%), sodium hyaluronate (0.05%), Tween 80 (0.05%), Na₂HPO₄.12H₂O (0.08%), sorbitol (5.46%), purified water added to 100 mL, pH 7.0-7.4, and mosm/L=295-305.
  • Composition L: cyclosporine A (0.2%), sodium hyaluronate (0.10%), Tween 80 (5.00%), Na₂HPO₄.12H₂O (0.08%), sorbitol (5.16%), purified water added to 100 mL, pH 7.0-7.4, and mosm/L=295-305.

The following composition is intended to mean that disclosed in Example 2 of U.S. Pat. No. 5,951,971, incorporated herein by reference. Composition M: cyclosporine A (0.025 g), polyoxyl 40 stearate (0.5 g), hydroxypropyl methylcellulose (0.2 g), butylated hydroxytoluene (0.0005 g), ethanol (0.1 g), sodium chloride (0.73 g), sodium dihydrogen phosphate (0.2 g), sodium edethate (0.1 g), sodium hydroxide to adjust pH to 6.0, and water to make 100 mL.

In another embodiment the composition provides more cyclosporin A than Composition A provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition A, wherein the drop of said composition and the drop of composition A are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition B provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition B, wherein the drop of said composition and the drop of composition B are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition C provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition C, wherein the drop of said composition and the drop of composition C are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition D provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition D, wherein the drop of said composition and the drop of composition D are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition E provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition E, wherein the drop of said composition and the drop of composition E are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition F provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition F, wherein the drop of said composition and the drop of composition F are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition G provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition G, wherein the drop of said composition and the drop of composition G are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition H provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition H, wherein the drop of said composition and the drop of composition H are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition I provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition I, wherein the drop of said composition and the drop of composition I are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition J provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition J, wherein the drop of said composition and the drop of composition J are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition K provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition K, wherein the drop of said composition and the drop of composition K are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition L provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition L, wherein the drop of said composition and the drop of composition L are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition M provides to the cornea of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition M, wherein the drop of said composition and the drop of composition M are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition A provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition A, wherein the drop of said composition and the drop of composition A are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition B provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition B, wherein the drop of said composition and the drop of composition B are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition C provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition C, wherein the drop of said composition and the drop of composition C are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition D provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition D, wherein the drop of said composition and the drop of composition D are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition E provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition E, wherein the drop of said composition and the drop of composition E are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition F provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition F, wherein the drop of said composition and the drop of composition F are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition G provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition G, wherein the drop of said composition and the drop of composition G are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition H provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition H, wherein the drop of said composition and the drop of composition H are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition I provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition I, wherein the drop of said composition and the drop of composition I are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition J provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition J, wherein the drop of said composition and the drop of composition J are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition K provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition K, wherein the drop of said composition and the drop of composition K are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition L provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition L, wherein the drop of said composition and the drop of composition L are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition M provides to the conjunctiva of a female New Zealand white rabbit 30 minutes after topical ocular administration of one drop of said composition or Composition M, wherein the drop of said composition and the drop of composition M are the same volume.

Comparison of two compositions in a person or animal can be carried out by, among other means, administering the claimed composition to one eye and the second composition to the second eye.

In another embodiment the composition provides more cyclosporin A than Composition A provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition A, wherein the drop of said composition and the drop of composition A are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition B provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition B, wherein the drop of said composition and the drop of composition B are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition C provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition C, wherein the drop of said composition and the drop of composition C are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition D provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition D, wherein the drop of said composition and the drop of composition D are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition E provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition E, wherein the drop of said composition and the drop of composition E are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition F provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition F, wherein the drop of said composition and the drop of composition F are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition G provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition G, wherein the drop of said composition and the drop of composition G are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition H provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition H, wherein the drop of said composition and the drop of composition H are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition I provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition I, wherein the drop of said composition and the drop of composition I are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition J provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition J, wherein the drop of said composition and the drop of composition J are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition K provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition K, wherein the drop of said composition and the drop of composition K are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition L provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition L, wherein the drop of said composition and the drop of composition L are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition M provides to the cornea of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition M, wherein the drop of said composition and the drop of composition M are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition A provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition A, wherein the drop of said composition and the drop of composition A are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition B provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition B, wherein the drop of said composition and the drop of composition B are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition C provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition C, wherein the drop of said composition and the drop of composition C are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition D provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition D, wherein the drop of said composition and the drop of composition D are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition E provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition E, wherein the drop of said composition and the drop of composition E are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition F provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition F, wherein the drop of said composition and the drop of composition F are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition G provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition G, wherein the drop of said composition and the drop of composition G are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition H provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition H, wherein the drop of said composition and the drop of composition H are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition I provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition I, wherein the drop of said composition and the drop of composition I are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition J provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition J, wherein the drop of said composition and the drop of composition J are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition K provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition K, wherein the drop of said composition and the drop of composition K are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition L provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition L, wherein the drop of said composition and the drop of composition L are the same volume.

In another embodiment the composition provides more cyclosporin A than Composition M provides to the conjunctiva of a female New Zealand white rabbit over a period of 24 hours after topical ocular administration of one drop of said composition or Composition M, wherein the drop of said composition and the drop of composition M are the same volume.

In one embodiment, wherein topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 500 ng of cyclosporin A per gram of cornea of said rabbit at 30 minutes after said topical administration.

In another embodiment, topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 2000 ng of cyclosporin A per gram of cornea of said rabbit at 30 minutes after said topical administration.

In another embodiment, topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 2400 ng of cyclosporin A per gram of cornea of said rabbit at 30 minutes after said topical administration.

In another embodiment, topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 17000 ng of cyclosporin A per gram of cornea of said rabbit over a period of 24 hours after said topical administration.

In another embodiment, topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the conjunctivas of said rabbit at least about 3300 ng of cyclosporin A per gram of conjunctiva of said rabbit over a period of 24 hours after said topical administration.

In another embodiment, said composition is an aqueous solution containing from 0.005% to about 0.04% cyclosporin A, wherein topical administration of one 35 μL drop of said composition to each eye of a New Zealand rabbit provides at least about 17000 ng of cyclosporin A per gram of cornea to the corneas of said rabbit as determined by:

• • topically administering said composition to each eye of each of 15 female New Zealand white rabbit test subjects, and determining the amount of cyclosporin A in the corneas of three subjects at times of about 0.5 hours, about 2 hours, about 6 hours, about 12 hours, and about 24 after administration to said subject,
    wherein the amount of cyclosporin A in the cornea is determined only once for each subject.

In another embodiment, said composition is an aqueous solution containing from 0.005% to about 0.04% cyclosporin A, wherein topical administration of one 35 μL drop of said composition to each eye of a New Zealand rabbit provides at least about 17000 ng of cyclosporin A per gram of conjunctiva to the conjunctivas of said rabbit as determined by:

• • topically administering said composition to each eye of each of 15 female New Zealand white rabbit test subjects, and determining the amount of cyclosporin A in the conjunctivas of three subjects at times of about 0.5 hours, about 2 hours, about 6 hours, about 12 hours, and about 24 after administration to said subject,
    wherein the amount of cyclosporin A in the conjunctiva is determined only a single time for each subject.

As mentioned above, these compositions are suitable for use in other mammals other than rabbits, including humans. Thus, any composition in the claims or elsewhere which is characterized by in vivo rabbit bioavailability testing is contemplated for use in a person or in another mammal. Defining a composition in terms of bioavailability in rabbits should not be construed to limit a method of treatment using the composition to use on rabbits, but treatment with the composition should be construed to include treatment on humans and other mammals.

The foregoing description details specific methods and compositions that can be employed to practice the present invention, and represents the best mode contemplated. However, it is apparent for one of ordinary skill in the art that further compositions with the desired pharmacological properties can be prepared in an analogous manner. Thus, however detailed the foregoing may appear in text, it should not be construed as limiting the overall scope hereof; rather, the ambit of the present invention is to be governed only by the lawful construction of the claims.

Claims

1. A method of treating ocular rosacea comprising topically administering to a mammal in need thereof a composition comprising cyclosporin A at a concentration of from about 0.0001% (w/v) to less than about 0.05% (w/v).

2. The method of claim 1 wherein the composition is an aqueous solution.

3. The method of claim 1 wherein the concentration of cyclosporin A is from about 0.005% (w/v) to about 0.04% (w/v).

4. The method of claim 2 wherein the concentration of cyclosporin A is from about 0.02% (w/v) to about 0.04% (w/v).

5. The method of claim 2 wherein the composition contains no ethanol.

6. The method of claim 2 wherein the composition contains no hyaluronic acid.

7. The method of claim 2 wherein the composition contains no cyclodextrin A.

8. The method of claim 6 wherein the composition contains no cyclodextrin.

9. The method of claim 8 wherein the composition contains no ethanol.

10. The method of claim 9 wherein the composition contains no hyaluronic acid.

11. The method of claim 2 wherein the composition is administered only once a day.

12. The method of claim 10 wherein the composition is administered only once a day.

13. The method of claim 1 wherein topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 500 ng of cyclosporin A per gram of cornea of said rabbit at 30 minutes after said topical administration.

14. The method of claim 12, wherein the mammal is a human.

15. The method of claim 1 wherein topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 1000 ng of cyclosporin A per gram of cornea of said rabbit at 30 minutes after said topical administration.

16. The method of claim 1 wherein topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 1400 ng of cyclosporin A per gram of cornea of said rabbit at 30 minutes after said topical administration.

17. The method of claim 1 wherein topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the corneas of said rabbit at least about 17000 ng·hr of cyclosporin A per gram of cornea of said rabbit over a period of 24 hours after said topical administration.

18. The method of claim 2 wherein topical administration of one 35 μL drop of said composition to each eye of a female New Zealand white rabbit provides to the conjunctivas of said rabbit at least about 3300 ng·hr of cyclosporin A per gram of conjunctiva of said rabbit over a period of 24 hours after said topical administration.

19. The method of claim 2 wherein said composition is an aqueous solution containing from 0.005% (w/v) to about 0.04% (w/v) cyclosporin A, wherein topical administration of one 35 μL drop of said composition to each eye of a New Zealand rabbit provides at least about 17000 ng·hr of cyclosporin A per gram of cornea to the corneas of said rabbit as determined by:

topically administering said composition to each eye of each of 15 female New Zealand white rabbit test subjects; and

determining the amount of cyclosporin A in the corneas of three subjects at times of about 0.5 hours, about 2 hours, about 6 hours, about 12 hours, and about 24 after administration to said subject;

wherein the amount of cyclosporin A in the cornea is determined only once for each subject.

20. The method of claim 2 wherein said composition is an aqueous solution containing from 0.005% (w/v) to about 0.04% (w/v) cyclosporin A, wherein topical administration of one 35 μL drop of said composition to each eye of a New Zealand rabbit provides at least about 6000 ng of cyclosporin A per gram of conjunctiva to the conjunctivas of said rabbit as determined by:

topically administering said composition to each eye of each of 15 female New Zealand white rabbit test subjects; and

determining the amount of cyclosporin A in the conjunctivas of three subjects at times of about 0.5 hours, about 2 hours, about 6 hours, about 12 hours, and about 24 after administration to said subject;

wherein the amount of cyclosporin A in the conjunctiva is determined only a single time for each subject.

21. The method of claim 1 wherein the mammal is a human patient, and wherein less than 10% of human patients suffer burning or stinging when said composition is administered only once a day for a period of three months.

22. The method of claim 1 wherein the composition contains a surfactant.

23. A method of treating ocular rosacea comprising topically administering to a mammal a multi-use composition comprising cyclosporin A at a concentration of from about 0.0001% (w/v) to less than about 0.2% (w/v), and an effective amount of a preservative.

24. The method of claim 61 wherein the preservative is an oxidizing preservative.

25. The method of claim 61 wherein the preservative is a cationic preservative.