US 7232572 B2 - Methods Of Treating Rosacea - The Lens - Free & Open Patent and Scholarly Search

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US 7232572 B2

Methods Of Treating Rosacea

Published: Jun 19, 2007
Earliest Priority: Apr 05 2001
Family: 18
Cited Works: 35
Cited by: 19
Cites: 21
Additional Info: Cited Works Full text Published

Abstract

A method of treating rosacea in a human in need thereof comprising administering to said human a tetracycline compound in an amount that is effective to treat rosacea, but has substantially no antibiotic activity.

Claims

A method for treating papules and pustules of rosacea in a human in need thereof comprising administering orally to said human a tetracycline compound, or a pharmaceutically acceptable salt thereof, in an amount that is effective to treat the papules and pustules of rosacea, but has substantially no antibiotic activity, said amount being 10-80% of the antibiotic amount, wherein the tetracycline compound is an antibiotic tetracycline compound or a pharmaceutically acceptable salt thereof administered in an amount that results in no reduction of skin microflora during a six-month treatment, without administering a bisphosphonate compound.
A method according to claim 1, wherein said tetracycline compound is minocycline or a pharmaceutically acceptable salt thereof administered in an amount which results in a serum concentration of 0.8 μg/ml.
A method according to claim 1, wherein said tetracycline compound is tetracycline or a pharmaceutically acceptable salt thereof administered in an amount which results in a serum concentration of 0.5 μg/ml.
A method according to claim 1, wherein said tetracycline compound is an antibiotic tetracycline compound or a pharmaceutically acceptable salt thereof administered in an amount which results in a serum concentration which is 10-80% of the minimum antibiotic serum concentration.
A method according to claim 4, wherein said antibiotic tetracycline compound is doxycycline, minocycline, tetracycline, oxytetracycline, chlortetracycline, demeclocycline or pharmaceutically acceptable salts of any such compound.
A method according to claim 5, wherein said antibiotic tetracycline compound is doxycycline or a pharmaceutically acceptable salt thereof.
A method according to claim 6, wherein said doxycycline or pharmaceutically acceptable salt thereof is administered in an amount which provides a serum concentration in the range of about 0.1 to about 0.8 μg/ml.
A method according to claim 6, wherein said doxycycline or pharmaceutically acceptable salt thereof is administered in an amount of 20 milligrams twice daily.
A method according to claim 7, wherein said doxycycline or pharmaceutically acceptable salt thereof is administered by sustained release.
A method according to claim 9, wherein said doxycycline or pharmaceutically acceptable salt thereof is administered in an amount of 40 milligrams.
A method according to claim 1, wherein said tetracycline compound is an antibiotic tetracycline compound or a pharmaceutically acceptable salt thereof administered in an amount which is 10-70% of the antibiotic amount.
A method according to claim 1, wherein said tetracycline compound is doxycycline or a pharmaceutically acceptable salt thereof.
A method according to claim 12, wherein said doxycycline is doxycycline monohydrate.
A method according to claim 12, wherein said doxycycline or pharmaceutically acceptable salt thereof is administered in an amount of 40 milligrams.
A method according to claim 14, wherein said doxycycline or pharmaceutically acceptable salt thereof is administered by sustained release.
A method according to claim 12, wherein said doxycycline or pharmaceutically acceptable salt thereof is administered twice a day in a dose of 20 mg.
A method according to claim 1, wherein said tetracycline compound is minocycline, tetracycline, oxytetracycline, chlortetracycline, demeclocycline or pharmaceutically acceptable salts of any such compound.
A method according to claim 4, wherein said tetracycline compound is doxycycline or a pharmaceutically acceptable salt thereof administered in an amount which results in a serum concentration of approximately 1.0 μg/ml.
A method according to claim 4, wherein said tetracycline compound is minocycline, tetracycline, oxytetracycline, chlortetracycline, demeclocycline or pharmaceutically acceptable salts of any such compound.
A method for treating papules and pustules of rosacea in a human in need thereof comprising administering orally to said human a hydrate of doxycycline in an amount that is effective to treat the papules and pustules of rosacea, but has substantially no antibiotic activity, said amount being 10-80% of the antibiotic amount, wherein the hydrate of doxycycline is administered in an amount that results in no reduction of skin microflora during a six-month treatment, said method not comprising administering a bisphosphonate compound.
A method according to claim 20, wherein said hydrate of doxycycline is doxycycline monohydrate.
A method according to claim 20 wherein said hydrate of doxycycline is administered in an amount which is 10-70% of the antibiotic amount.
A method according to claim 20, wherein said hydrate of doxycycline is administered in an amount of 40 milligrams.
A method according to claim 20, wherein said hydrate of doxycycline is administered by sustained release.
A method according to claim 20, wherein said hydrate of doxycycline is administered twice a day in a dose of 20 mg.
A method according to claim 23, wherein said hydrate of doxycycline is administered once a day.

Owners (US)

Galderma Laboratories Inc (Jul 29 2008)
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Collagenex Pharmaceuticals Inc (Jun 01 2005)
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Applicants

Collagenex Pharm Inc
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Inventors

Ashley Robert A
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CPC Classifications

A61K31/135
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A61K31/65
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A61K9/0053
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D06M16/00
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IPC Classifications

A01N37/18
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A61K31/65
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A61K9/20
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A61K9/48
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A61K9/68
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US Classifications

424/401
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424/440
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424/451
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424/464
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514/152
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Document History

Publication: Jun 19, 2007
US 7232572 B2
Application: Feb 18, 2005
US 6186605 A
Priority: Feb 18, 2005
US 6186605 A
Priority: Oct 15, 2002
US 27249902 A
Priority: Apr 5, 2002
US 11770902 A
Priority: Sep 26, 2001
US 32548901 P
Priority: Apr 5, 2001
US 28191601 P