US2006166938A1PendingUtilityA1
Method of treatment using bisphosphonic acid
Est. expiryMay 10, 2022(expired)· nominal 20-yr term from priority
A61P 19/06A61P 19/08A61P 19/00A61P 19/10A61K 31/663A61K 31/675A61K 9/2866A61K 9/2054A61K 9/2018A61K 31/662
56
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Claims
Abstract
The present invention refers to a pharmaceutical composition of a bisphosphonic acid or salt thereof, and an excipient thereof, and a method of treating disorder characterized by pathologically increased bone resorption comprising orally administering at least 150% of the expected efficacious daily dose of a bisphosphonic acid or a pharmaceutically acceptable salt thereof and one or more pharmaceutically acceptable excipients thereof and administering the dose at a period of one two or three consecutive days per month.
Claims
exact text as granted — not AI-modified1 . A method for treating or inhibiting osteoporosis comprising orally administering to a subject in need of such treatment, once monthly over a period of two consecutive days, about 50 mg to about 250 mg of a bisphosphonic acid or an amount of a pharmaceutically acceptable salt thereof that is equivalent to from about 50 mg to about 250 mg of said bisphosphonic acid.
2 . The method according to claim 1 comprising orally administering to a subject in need of such treatment, once monthly over a period of two consecutive days, about 100 mg to about 150 mg of bisphosphonic acid or an amount of a pharmaceutically acceptable salt thereof that is equivalent to about 100 mg to about 150 mg of said bisphosphonic acid.
3 . The method according to claim 2 , comprising orally administering to a subject in need of such treatment, once monthly over a period of two consecutive days, about 100 mg of bisphosphonic acid or an amount of a pharmaceutically acceptable salt thereof that is equivalent to about 100 mg of bisphosphonic acid.
4 . The method according to claim 2 , comprising orally administering to a subject in need of such treatment, once monthly over a period of two consecutive days, about 150 mg of bisphosphonic acid or an amount of a pharmaceutically acceptable salt thereof that is equivalent to about 150 mg of bisphosphonic acid.
5 . The method of claim 2 comprising orally administering to a subject in need of such treatment, once monthly over a period of two consecutive days, 100 mg of bisphosphonic acid or an amount of a pharmaceutically acceptable salt thereof that is equivalent to 100 mg of bisphosphonic acid.
6 . The method of claim 2 comprising orally administering to a subject in need of such treatment, once monthly over a period of two consecutive days, 150 mg of bisphosphonic acid or an amount of a pharmaceutically acceptable salt thereof that is equivalent to 150 mg of bisphosphonic acid.
7 . The method of claim 1 wherein said bisphosphonic acid is risedronic acid.
8 . The method of claim 2 wherein said bisphosphonic acid is risedronic acid.
9 . The method of claim 3 wherein said bisphosphonic acid is risedronic acid.
10 . The method of claim 4 wherein said bisphosphonic acid is risedronic acid.
11 . The method of claim 6 wherein said bisphosphonic acid is risedronic acid.
12 . The method of claim 2 wherein said bisphosphonic acid is administered in the form of a solid pharmaceutical composition.
13 . The method of claim 4 wherein said bisphosphonic acid is administered in the form of a solid pharmaceutical composition.
14 . The method of claim 6 wherein said bisphosphonic acid is administered in the form of a solid pharmaceutical composition.
15 . The method of claim 8 wherein said risedronic acid is administered in the form of a solid pharmaceutical composition.
16 . The method of claim 10 wherein said risedronic acid is administered in the form of a solid pharmaceutical composition.
17 . The method of claim 11 wherein said risedronic acid is administered in the form of a solid pharmaceutical composition.Join the waitlist — get patent alerts
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