US2008182827A2PendingUtilityA2
Method for the treatment of acne
Assignee: MEDICIS PHARMACEUTICAL CORPPriority: Jun 24, 2005Filed: Nov 21, 2007Published: Jul 31, 2008
Est. expiryJun 24, 2025(expired)· nominal 20-yr term from priority
A61P 31/02A61K 31/65A61P 17/10
64
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Claims
Abstract
A method for treatment of acne with tetracyclines is provided. A lower sustained dose and no loading dose is employed, with an optional once-a-day dosing regimen.
Claims
exact text as granted — not AI-modified1 - 5 . (canceled)
6 . An oral dosage form, comprising:
an antibiotically effective dose of an oral minocycline; and a pharmaceutically suitable delivery vehicle; wherein said oral dosage form is for administration once daily to provide a patient with about 0.5 mg/kg/day to about 1.5 mg/kg/day of said oral minocycline; and wherein said oral dosage form provides a continuous slow release, without a loading dose, of said oral minocycline, at a release rate in gastric fluid of either about 25% to about 52% within about 1 hour, about 53% to about 89% within about 2 hours, and at least about 90% within about 4 hours, or about 30% to about 52% within about 1 hour, about 53% to about 84% within about 2 hours, and at least about 85% within about 4 hours.
7 . The oral dosage form of claim 6 , wherein said oral minocycline is minocycline as hydrochloride.
8 . The oral dosage form of claim 6 , wherein said oral dosage form is for administration once daily to provide said patient with about 1.0 mg/kg/day of said oral minocycline.
9 . An oral dosage form, comprising:
an antibiotically effective dose of an oral minocycline; and a pharmaceutically suitable delivery vehicle; wherein said oral dosage form is for administration once daily to provide a patient with about 0.5 mg/kg/day to about 1.5 mg/kg/day of said oral minocycline; and wherein said oral dosage form does not provide an immediate release of said oral minocycline, and provides a continuous slow release, without a loading dose, of said oral minocycline at a rate so that C max is reached at about 3.5 hours after administration to said patient.
10 . The oral dosage form of claim 9 , wherein said oral minocycline is minocycline as hydrochloride.
11 . The oral dosage form of claim 9 , wherein said oral dosage form is for administration once daily to provide said patient with about 1.0 mg/kg/day of said oral minocycline.
12 . An oral dosage form, comprising:
an antibiotically effective dose of an oral minocycline; a fast dissolving carrier; and a slow dissolving carrier, wherein said fast dissolving carrier and said slow dissolving carrier are at a weight ratio of about 0.3 to about 0.5 that provides a continuous, slow release, without immediate release, of said oral minocycline; and wherein said oral dosage form is for administration once daily to provide a patient with about 0.5 mg/kg/day to about 1.5 mg/kg/day of said oral minocycline.
13 . The oral dosage form of claim 12 , wherein said oral minocycline is minocycline as hydrochloride.
14 . The oral dosage form of claim 12 , wherein said weight ratio of fast dissolving carrier to slow dissolving carrier is 0.35 to 0.45.
15 . The oral dosage form of claim 14 , wherein said weight ratio of fast dissolving carrier to slow dissolving carrier is 0.36 to 0.40.
16 . The oral dosage form of claim 12 , wherein said oral dosage form is for administration once daily to provide said patient with about 1.0 mg/kg/day of said oral minocycline.
17 . The oral dosage form of claim 12 , further comprising an intragranular fast dissolving carrier.
18 . The oral dosage form of claim 17 , wherein said slow dissolving carrier encapsulates said intragranular fast dissolving carrier.
19 . The oral dosage form of claim 18 , further comprising a coating.Cited by (0)
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