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Patent Analysis of

Therapeutic or preventive agent for meibomian gland dysfunction or meibomian gland blockage

Updated Time 12 June 2019

Patent Registration Data

Publication Number

US9999594

Application Number

US15/363583

Application Date

29 November 2016

Publication Date

19 June 2018

Current Assignee

SANTEN PHARMACEUTICAL CO., LTD.

Original Assignee (Applicant)

SANTEN PHARMACEUTICAL CO., LTD.

International Classification

A61K31/7048,A61K47/38,A61K9/10,A61K9/08,A61K9/06

Cooperative Classification

A61K9/0048,A61K9/06,A61K9/08,A61K47/38,A61K31/7048

Inventor

KIDO, KAZUTAKA,NAGANO, TAKASHI

Abstract

The objective of the present invention is to provide a new medicinal use of clarithromycin. The present invention is a therapeutic agent or a preventive agent for meibomian gland dysfunction or meibomian gland blockage and comprises clarithromycin as an active ingredient. The dosage form is preferably an eye drop or eye ointment.

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Claims

1. A method for therapy of meibomian gland dysfunction with obstructions of meibomian gland orifices, the method comprising administering an effective amount of clarithromycin to a subject in need thereof.

2. The method according to claim 1, wherein an effective amount of clarithromycin is administered in a dosage form of an ophthalmic solution or ophthalmic ointment.

3. The method according to claim 1, wherein clarithromycin is administered in a dosage form of an ophthalmic solution in an amount of from 0.0001 to 5% (w/v).

4. The method according to claim 1, wherein clarithromycin is administered in a dosage form of an ophthalmic solution in an amount of from 0.01 to 3 (w/v).

5. A method for improving meibomian gland obstruction, wherein the meibomian gland obstruction is caused by reduced secretion type meibomian gland dysfunction, the method comprising administering an effective amount of clarithromycin to a subject in need thereof.

6. The method according to claim 5, wherein an effective amount of clarithromycin is administered in a dosage form of an ophthalmic solution or ophthalmic ointment.

7. The method according to claim 5, wherein clarithromycin is administered in a dosage form of an ophthalmic solution in an amount of from 0.0001 to 5% (w/v).

8. The method according to claim 5, wherein clarithromycin is administered in a dosage form of an ophthalmic solution in an amount of from 0.01 to 3 (w/v).

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Claim Tree

  • 1
    1. A method for therapy of meibomian gland dysfunction with obstructions of meibomian gland orifices, the method comprising
    • administering an effective amount of clarithromycin to a subject in need thereof.
    • 2. The method according to claim 1, wherein
      • an effective amount of clarithromycin is administered in a dosage form of an ophthalmic solution or ophthalmic ointment.
    • 3. The method according to claim 1, wherein
      • clarithromycin is administered in a dosage form of an ophthalmic solution in an amount of from 0.0001 to 5% (w/v).
    • 4. The method according to claim 1, wherein
      • clarithromycin is administered in a dosage form of an ophthalmic solution in an amount of from 0.01 to 3 (w/v).
  • 5
    5. A method for improving meibomian gland obstruction, wherein
    • the meibomian gland obstruction is caused by reduced secretion type meibomian gland dysfunction, the method comprising
    • 6. The method according to claim 5, wherein
      • an effective amount of clarithromycin is administered in a dosage form of an ophthalmic solution or ophthalmic ointment.
    • 7. The method according to claim 5, wherein
      • clarithromycin is administered in a dosage form of an ophthalmic solution in an amount of from 0.0001 to 5% (w/v).
    • 8. The method according to claim 5, wherein
      • clarithromycin is administered in a dosage form of an ophthalmic solution in an amount of from 0.01 to 3 (w/v).
See all independent claims <>

Description

TECHNICAL FIELD

The present invention relates to a therapeutic or preventive

agent for meibomian gland dysfunction or meibomian gland concretion.

BACKGROUND ART

There are approximately 25 meibomian glands in the upper eyelid and approximately 20 meibomian glands in the lower eyelid of the human eye, and lipids are secreted from the meibomian gland orifices. Meibomian gland dysfunction (MGD) is a condition where a diffuse abnormality of the function of the meibomian glands is induced by various causes, and is accompanied by chronic ocular discomfort. Further, meibomian gland concretion is a condition where meibomian glands are obstructed by a white non-opaque oily clot formed in the duct because of decreased meibomian gland function.

On the other hand, clarithromycin is a macrolide antibiotic, which has been used for therapy of pharyngitis, tonsillitis, pneumonia, skin infections, acute exacerbation of chronic bronchitis and the like based on its antibacterial effect. Recently, aside from antibacterial effects, clarithromycin has been found to have antiinflammatory, immunoregulatory, and antibacterial biofilm effects, and based on these novel effects, starting with the therapy of endometriosis or fibroids, gastrointestinal disorders, and pruritus, the use of clarithromycin has also been proposed for acute exacerbation of chronic bronchitis, bronchial asthma, influenza virus infection, atopic dermatitis, rheumatoid arthritis, etc. (Patent Publications 1, 2, and 3).

Patent Document 1: Japanese Unexamined Patent Application, Publication No. 2006-241172

Patent Document 2: Japanese Unexamined Patent Application, Publication No. H06-92850

Patent Document 3: Japanese Unexamined Patent Application, Publication No. H11-147827

DISCLOSURE OF THE INVENTION

Problems to be Solved by the Invention

Thus, the investigation of novel medical applications of clarithromycin is a subject of great interest.

Means for Solving the Problems

The present inventors sought and diligently researched novel medical applications of clarithromycin, and discovered that (1) in tests of meibomian gland peripheral telangiectasia due to the administration of complete Freund's adjuvant using rats, clarithromycin notably improved the telangiectasia score, and (2) in tests of obstruction meibomian gland orifices due to feeding an HR-AD diet using hairless mice, clarithromycin notably reduced the number of obstructions of the meibomian gland orifices, and improved the obstructions, and thus completed the present invention.

Namely, the present invention is therapeutic agent or preventive agent for meibomian gland dysfunction or meibomian gland concretion comprising clarithromycin as the effective component.

Effects of the Invention

Thus, it is expected that a formulation comprising clarithromycin as the effective component will be effective for therapy or prevention of meibomian gland dysfunction or meibomian gland concretion.

PREFERRED MODE FOR CARRYING OUT THE INVENTION

Below, embodiments of the present invention are explained.

The clarithromycin of the present invention can be easily produced by a conventional method, or obtained commercially.

Meibomian gland dysfunction (MGD) is a condition where diffuse abnormality of the meibomian glands is induced by various causes, and is accompanied with chronic ocular discomfort. Meibomian gland dysfunction can be categorized by a condition of the secretion of the meibomian glands, and can be divided into reduced secretion type and increased secretion type, and in clinical practice, the reduced secretion type is more common than the increased secretion type.

Reduced secretion type meibomian gland dysfunction is a condition where the secretion of the meibomian lipid is reduced by the accumulation of excess keratinized substances in the duct of the meibomian gland, or by the obstruction of the meibomian gland orifices by various causes. Finding of obstructions of the meibomian gland orifices or finding of abnormalities surrounding the meibomian gland orifices (telangiectasia, displacement of the mucocutaneous junction, irregularity of the eyelid margins, and the like) are considered to be pathognomic findings of reduced secretion type meibomian gland dysfunction.

Increased secretion type meibomian gland dysfunction is a disorder where lipid secretion of the meibomian glands is excessive, and has the characteristic that large quantities of meibomian gland lipids are discharged to the eyelid margins in reaction to compression of the tarsus.

Meibomian gland concretion is a condition where a mixture of keratinized substances and lipids is concreted in the duct of the meibomian gland, and obstruction of the orifice of the meibomian gland is considered as a characteristic finding.

As induced symptoms accompanying meibomian gland dysfunction or meibomian gland concretion, there are many symptoms such as ocular discomfort, burning sensations, itching and the like.

The therapeutic agent or preventive agent for meibomian gland dysfunction or meibomian gland concretion of the present invention can be administered orally or parenterally. As the dosage form, dosage forms for parenteral use such as ophthalmic solutions, ophthalmic ointments, injections and the like, and dosage forms for oral administration such as tablets, capsules, granules, powders and the like may be mentioned, and in particular, ophthalmic solutions are particularly preferable.

The formulation thereof can be carried out using generally used techniques. For example, in the case of an ophthalmic solution, a tonicity agent such as sodium chloride or concentrated glycerin and the like; a buffer such as sodium phosphate, sodium acetate and the like; a surfactant such as polyoxyethylene sorbitan monooleate, polyoxyl 40 stearate, polysorbate 80, polyoxyethylene hydrogenated castor oil and the like; a stabilizer such as sodium citrate or sodium edetate and the like; and a preservative such as benzalkonium chloride, paraben and the like; and the like may be used as needed. The pH may be within the allowable range of ophthalmic solutions, and is preferably in the range of 4 to 8.

In the case of an ophthalmic ointment, the formulation may be carried out using a general purpose base such as white petrolatum, liquid paraffin, and the like.

In the case of oral preparations such as tablets, capsules, granules, powders and the like, the formulation may be carried out using an extender such as lactose, crystalline cellulose, starch, vegetable oil and the like; a lubricant such as magnesium stearate, talc and the like; a binder such as hydroxypropyl cellulose, polyvinyl pyrrolidone and the like, a disintegrant such as carboxylmethyl cellulose calcium, low-substituted hydroxypropylmethyl cellulose and the like, a coating agent such as hydroxypropylmethyl cellulose, macrogol, a silicon resin and the like; a film forming agent such as gelatin film and the like; and the like, as needed.

The dose of clarithromycin can be properly selected depending on the symptoms, age, dosage form and the like, and in the case of an ophthalmic solution, a formulation of from 0.0001 to 5% (w/v), preferably from 0.01 to 3% (w/v), may be dropped into the eye on the order of from 1 to 6 times/day. In the case of an oral preparation, clarithromycin may be usually administered at from 0.1 to 5000 mg per day, preferably 1 to 1000 mg per day, at once or divided into several doses.

The present invention includes the following inventions.

(1) Clarithromycin for use in the therapy or prevention of MGD or meibomian gland concretion.

(2) Clarithromycin as recited above in item (1) formulated as a dosage form of an ophthalmic solution or an ophthalmic ointment.

(3) Use of clarithromycin for manufacturing a medicament for therapy or prevention of MGD or meibomian gland concretion.

(4) The use as recited above in item (3) wherein the dosage form of the medicament is an ophthalmic solution or an ophthalmic ointment.

EXAMPLES

Hereinafter, preparation examples and results of pharmacological tests are shown, but these examples are to facilitate understanding of the present invention and do not limit the scope of the present invention.

Preparation Example 1

In 100 ml,

Clarithromycin 1 g

Concentrated glycerin 2 g

Dibasic sodium phosphate hydrate 0.1 g

Polyoxyl 40 stearate 0.1 g

Diluted hydrochloric acid/sodium hydroxide q.s.

Sterile purified water q.s.

pH 7.0

By altering the amount of clarithromycin to be added, solution-type ophthalmic solutions at concentrations of 0.01% (w/v), 0.1% (w/v) or 1.0% (w/v) could be prepared.

Preparation Example 2

In 100 ml,

Clarithromycin 1 g

Sodium chloride 0.75 g

Disodium hydrogen phosphate 0.06 g

Sodium dihydrogen phosphate 0.6 g

Polysorbate 80 0.005 g

Hydroxypropyl methyl cellulose 0.001 g

Sodium edetate hydrate 0.01 g

Diluted hydrochloric acid/sodium hydroxide q.s.

Sterile purified water q.s.

pH 7.0

By altering the amount of clarithromycin to be added, suspension-type ophthalmic solutions at concentrations of 0.1% (w/v) or 0.5% (w/v) could be prepared.

Preparation Example 3

In 100 ml,

Clarithromycin 2 g

Liquid paraffin 30 g

White soft paraffin q.s.

By altering the amount of clarithromycin to be added, ophthalmic ointments at concentrations of 1% (w/w) or 5% (w/w) could be prepared.

Pharmacological Tests

1. Test for Meibomian Gland Peripheral Telangiectasia by Administration of Full Friend's Adjuvant Using Rats

(Method for Preparation of Test Sample)

Clarithromycin (LKT Laboratories, Inc.), concentrated glycerin, dibasic sodium phosphate hydrate and polyoxyl 40 stearate were added to purified water and dissolved to prepare a test sample comprising clarithromycin at a final concentration of 1% (w/v), at pH 7.

(Test Method)

Twenty five μl of complete Freund's adjuvant was administered to one site of the right upper eyelid of female Lewis rats at five weeks age. On the seventh day from the initiation, the periphery of the meibomian gland orifices on the right upper eyelid was observed using a slit-lamp and a telangiectasia score was determined. The eyelid margin of the upper eyelid was divided into three segments: ear, middle and nasal sites, and based on criteria described in Table 1, scores of telangiectasia peripheral to the meibomian gland orifices in each segment were determined and the sum of the scores in three segments were calculated as the telangiectasia score of one eye. The presence or absence of dilation of the capillaries was determined based on whether a capillary that is usually not visible could be ascertained as a result of enlargement of the capillary diameter.


TABLE 1
Condition of telangiectasia in the vicinity of meibomian gland
Score
orifices
0
Dilation of the capillaries is not recognized at the periphery
of the meibomian gland orifices when eyelid is in opened state.
1
Dilation of a few capillaries is recognized at the periphery
of the meibomian gland orifices when eyelid is in opened state.
2
Moderate dilation of the capillaries or slight redness is visible
at the periphery of the meibomian gland orifices when eyelid is in
opened state.
3
Redness and severe telangiectasia are visible surrounding
meibomian gland orifices when eyelid is in opened state.

After dividing into a saline-administered group and a 1% (w/v) clarithromycin aqueous solution-administered groups, the test was carried out with six eyes in each group so as to minimize variations in mean scores, and from the 8th day after initiation, saline (5 μl/eye, six times per day) or 1% (w/v) clarithromycin aqueous solution (5 μl/eye, three or six times per day) were instilled into the right eyes for 21 days. At 28 days after initiation, the peripheries of the meibomian gland orifices on the right upper eyelids were observed using a slit-lamp and the telangiectasia score was determined.

(Results)

The results (the means of the telangiectasia scores) are shown in Table 2.


TABLE 2
Telangiectasia score
7 days after
28 days after
initiation
initiation
(day 0 from start
(day 21 from start
of administration)
of administration)
Saline-administered group
5.3
4.3
1% clarithromycin aqueous
5.3
2.8
solution-administered group
(instilled 3 times per day)
1% clarithromycin aqueous
5.3
2.5
solution-administered group
(instilled 6 times per day)

(Discussion)

At seven days from the initiation (day 0 from the start of administration), no difference was recognized in the means of the telangiectasia scores of each group, but 28 days after initiation (day 21 from the start of administration), the telangiectasia score in the vicinity of the meibomian gland orifices in the 1% clarithromycin aqueous solution-administered group (instilled three or six times per day) was remarkably lower compared to the saline-administered group.

2. Test for Obstruction of Meibomian Gland Orifices by Feeding HR-AD Diet Using Hairless Mice

(Method for Preparation of Test Sample)

A 1% (w/v) clarithromycin test solution was prepared by the same operation as described in Pharmacological Test 1.

(Test Method)

Male Hos:HR-1 hairless mice at five weeks of age were divided into a group of 6 fed a regular diet (CRF-1 diet, manufactured by Oriental Yeast Co., Ltd.); and a group of 12 fed an HR-AD diet (manufactured by Nosan Corporation), and the mice in each respective group were freely allowed to feed the regular diet or HR-AD diet. On the 28th day after the start of the diets, meibomian gland orifices were observed using a slit-lamp and the number of obstructed orifices out of eight meibomian gland orifices of the center of the right upper eyelid were counted. The presence or absence of an obstruction of the meibomian gland orifice was determined based on whether the meibomian gland orifice was in a cloudy and swollen state.

The 12 mice in the HR-AD diet group were further divided into a saline-administered group; and a 1% (w/v) clarithromycin aqueous solution-administered group, and testing was carried out with six eyes in each group so as to minimize variations in the mean scores of the number of obstructed meibomian gland orifices in each group; from the 29th day after starting the diets, saline (2 μl/eye, three times per day) or 1% (w/v) clarithromycin aqueous solution (2 μl/eye, three times per day) were instilled for 14 days. At 42 days after starting the diet, meibomian gland orifices were observed using a slit-lamp and the number of obstructed orifices out of eight meibomian gland orifices of the center of the right upper eyelid were counted.

(Results)

The results (the means of the number of obstructed orifice scores) are shown in Table 3.


TABLE 3
Number of obstructed
meibomian gland orifices
28 days after
42 days after
starting feeding
starting feeding
(day 0 from start
(day 14 from start
of administration)
of administration)
Non-treated group
0.8
1.0
(group fed a regular diet)
Saline-administered group
5.3
4.5
1% clarithromycin aqueous
5.5
1.8
solution-administered group

(Discussion)

At 28 days from starting the diet (day 0 from starting the administration), there was almost no difference in the number of obstructed meibomian gland orifices between the saline-administered group (fed by HR-AD diet) and the 1% (w/v) clarithromycin aqueous solution-administered group (fed by HR-AD diet), but 42 days after starting the diet (14 days from starting administration), the number of obstructed meibomian gland orifices was remarkably decreased, and meibomian gland concretion was improved in the 1% (w/v) clarithromycin aqueous solution-administered group.

INDUSTRIAL APPLICABILITY

In the present invention, by using clarithromycin as an effective component, it is possible to treat or prevent MGD or meibomian gland concretion.

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Patent Valuation

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30.0/100 Score

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100.0/100 Score

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65.14/100 Score

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It shows the degree of innovation that can be derived from a company’s IP. Here we look into ease of detection, ability to design around and significance of the patented feature to the product/service.

60.0/100 Score

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It takes the R&D behavior of the company itself into account that results in IP. During the invention phase, larger companies are considered to assign a higher R&D budget on a certain technology field, these companies have a better influence on their market, on what is marketable and what might lead to a standard.

21.47/100 Score

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Citation

Patents Cited in This Cited by
Title Current Assignee Application Date Publication Date
一种克拉霉素药物制剂 广州贝氏药业有限公司 24 June 2003 18 February 2004
一种含大环内酯抗生素的缓释制剂 济南康泉医药科技有限公司 22 May 2006 25 October 2006
Therapeutic Compositions for the Treatment of Dry Eye Disease SCHEPENS EYE RESEARCH INSTITUTE 25 February 2011 25 August 2011
一种克拉霉素注射剂 广州贝氏药业有限公司 20 May 2003 05 November 2003
子宮内膜症の予防又は治療薬 菅又 昌雄 19 June 2006 14 September 2006
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