US2019091244A1PendingUtilityA1
Methods of treating acne
Est. expiryApr 5, 2021(expired)· nominal 20-yr term from priority
Inventors:Robert Ashley
A61K 31/135D06M 16/00A61P 17/10A61K 31/65A61K 9/0053
70
PatentIndex Score
0
Cited by
0
References
0
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-modified1 .- 17 . (canceled)
18 . A method for treating acne in a human in need thereof, the method comprising administering orally to the human doxycycline, or a pharmaceutically acceptable salt thereof, in an amount that is 5 mg to 40 mg total daily dose of doxycycline.
19 . The method according to claim 18 , wherein the doxycycline, or a pharmaceutically acceptable salt thereof, is administered in an amount of 40 milligrams.
20 . The method according to claim 19 , wherein the doxycycline, or a pharmaceutically acceptable salt thereof, is administered by sustained release.
21 . The method according to claim 20 , wherein the doxycycline, or a pharmaceutically acceptable salt thereof, is administered once a day.
22 . The method according to claim 18 , wherein the doxycycline, or a pharmaceutically acceptable salt thereof, is administered in a dose of 20 mg twice a day.
23 . The method according to claim 18 , wherein the 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.
24 . The method according to claim 18 , wherein the method results in no reduction in skin microflora during a six month treatment.
25 . The method according to claim 18 , wherein the doxycycline is doxycycline monohydrate.
26 . The method according to claim 18 , wherein the doxycycline is doxycycline hyclate.
27 . A method for treating acne in a human in need thereof, the method comprising administering orally to the human doxycycline, or a pharmaceutically acceptable salt thereof, in an amount that (i) is 5 mg to 40 mg total daily dose of doxycycline and (ii) results in no reduction of skin microflora during a six-month treatment.
28 . The method according to claim 27 , wherein the doxycycline, or a pharmaceutically acceptable salt thereof, is administered in an amount of 40 milligrams.
29 . The method according to claim 28 , wherein the doxycycline, or a pharmaceutically acceptable salt thereof, is administered by sustained release.
30 . The method according to claim 29 , wherein the doxycycline is administered once a day.
31 . The method according to claim 27 , wherein the doxycycline, or a pharmaceutically acceptable salt thereof, is administered in a dose of 20 mg twice a day.
32 . The method according to claim 27 , wherein the 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.
33 . The method of according to claim 27 , wherein the doxycycline is doxycycline monohydrate.
34 . The method of according to claim 27 , wherein the doxycycline is doxycycline hyclate.Join the waitlist — get patent alerts
Track US2019091244A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.