US2003216439A1PendingUtilityA1
Use of an H+, K+-ATPase inhibitor in the treatment of asthma
Priority: Oct 11, 1996Filed: Jun 11, 2003Published: Nov 20, 2003
Est. expiryOct 11, 2016(expired)· nominal 20-yr term from priority
A61K 31/435A61K 31/4184A61K 31/4439A61K 31/573A61K 9/0014A61K 45/06A61K 31/437A61K 31/56A61K 31/58
57
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Claims
Abstract
The invention provides a method for the treatment of polyposis which comprises treating a subject suffering from polyposis with an H + , K + -ATPase inhibitor and, optionally, a glucocorticoid. The invention also relates to a pharmaceutical formulation for simultaneous, separate or sequential administration in the treatment of Widal's Syndrome and in the treatment of asthma.
Claims
exact text as granted — not AI-modified1 . Use of an H + , K + -ATPase inhibitor in the manufacture of a medicament for the treatment of nasal polyps.
2 . Use of an H + , K + -ATPase inhibitor in the manufacture of a medicament for the treatment of Widal's Syndrome.
3 . Use of an H + , K + -ATPase inhibitor and a glucocorticoid in the manufacture of a pharmaceutical formulation intended for simultaneous, separate or sequential administration in the treatment of Widal's Syndrome.
4 . Use of an H + , K + -ATPase inhibitor and a glucocorticoid in the manufacture of a pharmaceutical formulation intended for simultaneous, separate or sequential administration in the treatment of asthma.
5 . Use according to claim 3 wherein the glucocorticoid is a topically active anti-inflammatory steroid.
6 . Use according to claim 4 wherein the glucocorticoid is budesonide, beclomethasone dipropionate or fluticasone propionate.
7 . Use according to any one of the preceding claims wherein the H + , K + -ATPase inhibitor is a compound of formula
wherein N in the benzimidazole moiety of Het 2 means that one of the ring carbon atoms substituted by R 6 -R 9 optionally may be exchanged for a nitrogen atom without any substituents;
R 1 and R 3 each independently represent hydrogen, alkyl, or alkoxy on the condition that R 1 and R 3 do not simultaneously represent alkoxy; and R 2 represents alkyl, alkoxy optionally substituted by fluorine, alkylthio or alkoxyalkoxy; or one of R 1 and R 3 is halogen and the other is hydrogen and R 2 is 1-morpholino, 1-piperidino or dialkylamino;
R 4 and R 5 are the same or different and selected from hydrogen and alkyl;
R 6 -R 9 are the same or different and selected from hydrogen, halogen, alkyl, alkoxy, haloalkoxy, alkylcarbonyl, and alkoxycarbonyl;
R 10 is hydrogen or R 10 and R 3 together complete a ring containing 6 to 8 carbon atoms; and
R 11 represents hydrogen, halogen or alkyl;
wherein the compound of formula (I) is optionally in the form of a pharmaceutically acceptable alkaline salt or in its neutral form or is a single enantiomer or a racemic mixture thereof;
wherein each alkyl or alkylenyl moiety has a branched or straight chain and has 1 to 6 carbon atoms.
8 . Use according to claim 7 wherein the compound of formula (I) is a compound of formula
or an alkaline salt thereof, or the (−)-enantiomer or an alkaline salt of the (−)-enantiomer.
9 . A method for the treatment of nasal polyps which method comprises treating a subject suffering from the said condition with a pharmaceutical formulation comprising an H + , K + -ATPase inhibitor.
10 . A method for the treatment of Widal's Syndrome which comprises treating a subject suffering from the syndrome with a pharmaceutical formulation comprising an H + , K + -ATPase inhibitor.
11 . A method for the treatment of Widal's Syndrome which comprises simultaneously, separately or sequentially administration to a subject suffering from the syndrome with a pharmaceutical formulation comprising an H + , K + -ATPase inhibitor and a glucocorticoid.
12 . A method for the treatment of asthma which comprises simultaneously, separately or sequentially administration to a subject suffering from the syndrome with a pharmaceutical formulation comprising an H + , K + -ATPase inhibitor and a glucocorticoid.
13 . A method according to claim 11 wherein the glucocorticoid is a glucocorticoid defined in claim 5 or 6 .
14 . A method according to any one of claims 9 to 13 wherein the H + , K + -ATPase inhibitor is a compound of the formula defined in claim 7 or 8 .
15 . A pharmaceutical formulation for simultaneous, separate or sequential use in the treatment of Widal's Syndrome which formulation comprises an H + , K + -ATPase inhibitor and a glucocorticoid.
16 . A pharmaceutical formulation for simultaneous, separate or sequential administration in the treatment of asthma which pharmaceutical formulation comprises an H + , K + -ATPase inhibitor and a glucocorticoid.
17 . A pharmaceutical formulation according to claim 15 or 16 wherein the glucocorticoid is a glucocorticoid defined in claim 5 or 6 .
18 . A pharmaceutical formulation according to any of claims 15 - 17 wherein the H + , K + -ATPase inhibitor is a compound of the formula defined in claim 7 or 8 .Join the waitlist — get patent alerts
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