US2014100200A1PendingUtilityA1
Methods of treating acne
Est. expiryApr 5, 2021(expired)· nominal 20-yr term from priority
Inventors:Robert Ashley
A61K 31/135A61K 31/65A61P 17/10D06M 16/00A61K 9/0053
72
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Claims
Abstract
A method of treating acne in a human in need thereof comprising administering systemically to said human a tetracycline compound in an amount that is effective to treat acne but has substantially no antibiotic activity, without administering a bisphosphonate compound.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for treating acne in a human in need thereof, the method comprising
administering orally to said human doxycycline, or a pharmaceutically acceptable salt thereof, in an amount that (i) is effective to treat acne; (ii) is 10-80% of a 50 mg dose of doxycycline; and (iii) results in no reduction of skin microflora during a six-month treatment, without administering a bisphosphonate compound.
2 . The method according to claim 1 , wherein said doxycycline is doxycycline monohydrate.
3 . The method according to claim 2 , wherein said doxycycline monohydrate is administered in an amount of 40 milligrams.
4 . The method according to claim 3 , wherein said doxycycline monohydrate is administered by sustained release.
5 . A method according to claim 4 , wherein said doxycycline monohydrate is administered once a day.
6 . The method according to claim 2 , wherein said doxycycline monohydrate is administered in a dose of 20 mg twice a day.
7 . The method according to claim 1 , wherein said doxycycline, or a 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.
8 . A method for treating acne in a human in need thereof, the method comprising
administering orally to said human doxycycline, or a pharmaceutically acceptable salt thereof, in an amount that (i) is effective to treat acne; (ii) is 40-80% of a 50 mg dose of doxycycline; and (iii) results in no reduction of skin microflora during a six-month treatment, without administering a bisphosphonate compound.
9 . The method according to claim 8 , wherein said doxycycline is doxycycline monohydrate.
10 . The method according to claim 9 , wherein said doxycycline monohydrate is administered in an amount of 40 milligrams.
11 . The method according to claim 10 , wherein said doxycycline monohydrate is administered by sustained release.
12 . A method according to claim 11 , wherein said doxycycline monohydrate is administered once a day.
13 . The method according to claim 9 , wherein said doxycycline monohydrate is administered in a dose of 20 mg twice a day.
14 . The method according to claim 8 , wherein said doxycycline, or a 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.
15 . A method for treating acne in a human in need thereof, the method comprising
administering orally to said human doxycycline, or a pharmaceutically acceptable salt thereof, in an amount of 40 mg per day, wherein the amount results in no reduction of skin microflora during a six-month treatment, without administering a bisphosphonate compound.
16 . The method according to claim 15 , wherein said doxycycline is doxycycline monohydrate.
17 . The method according to claim 16 , wherein said doxycycline monohydrate is administered by sustained release.
18 . A method according to claim 17 , wherein said doxycycline monohydrate is administered once a day.
19 . The method according to claim 16 , wherein said doxycycline monohydrate is administered in a dose of 20 mg twice a day.
20 . The method according to claim 15 , wherein said doxycycline, or a 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.Cited by (0)
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