Aldosterone receptor antagonist and alpha-adrenergic modulating agent combination therapy for prevention or treatment of pathogenic conditions
OwnerEllen G. McMahon, Amy Rudolphinventors
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OwnerEllen G. McMahon, Amy Rudolphinventors
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A combination therapy comprising a therapeutically-effective amount of an aldosterone receptor antagonist and a therapeutically-effective amount of an alpha-adrenergic modulating agent is described for treatment of circulatory disorders, including cardiovascular disorders such as hypertension, congestive heart failure, cirrhosis and ascites. Preferred alpha-adrenergic modulating agents are those compounds having high potency and bioavailability. Preferred aldosterone receptor antagonists are 20-spiroxane steroidal compounds characterized by the presence of a 9α,11α-substituted epoxy moiety. A preferred combination therapy includes an alpha-1-adrenergic antagonist or an alpha-2-adrenergic agonist and the aldosterone receptor antagonist epoxymexrenone.
A combination for the treatment or prevention of a cardiovascular disorder comprising a first amount of an aldosterone receptor antagonist and a second amount of an alpha-adrenergic modulating agent, wherein said first amount and said second amount together comprise a therapeutically-effective amount of said aldosterone receptor antagonist and said alpha-adrenergic modulating agent, and wherein said alpha-adrenergic modulating agent is selected from the group consisting of amosulalol, arotinolol, dapiprazole, fenspirlde, indoramin, naftopidil, nicergoline, tamsulosin, tolazoline, trimazosin, yohimbine, phenoxybenzamine, phentolamine, bunazosin, urapidil, alfuzosin, ketanserin, monatepil, SUN 9221, S-2150, apraclonidine, guanfacil, rilmenidine, and moxonidine.
A pharmaceutical composition for the treatment or prevention of a cardiovascular disorder comprising a first amount of an aldosterone receptor antagonist, a second amount of an alpha-adrenergic modulating agent, and one or more pharmaceutically acceptable carrier materials, wherein said first amount and said second amount together comprise a therapeutically-effective amount of said aldosterone receptor antagonist and said alpha-adrenergic modulating agent, and wherein said alpha-adrenergic modulating agent is selected from the group consisting of amosulalol, arotinolol, dapiprazole, fenspirlde, indoramin, naftopidil, nicergoline, tamsulosin, tolazoline, trimazosin, yohimbine, phenoxybenzamine, phentolamine, bunazosin, urapidil, alfuzosin, ketanserin, monatepil, SUN 9221, S-2150, apraclonidine, guanfacil, rilmenidine, and moxonidine.
A method for the treatment or prevention of a cardiovascular disorder in a subject susceptible to or afflicted with such disorder comprising administering to the subject a first amount of an aldosterone receptor antagonist and a second amount of an alpha-adrenergic modulating agent, wherein said first and second amount together comprise a therapeutically-effective amount of said aldosterone receptor antagonist and said alpha-adrenergic modulating agent, and wherein said alpha-adrenergic modulating agent is selected from the group consisting of amosulalol, arotinolol, dapiprazole, fenspirlde, indoramin, naftopidil, nicergoline, tamsulosin, tolazoline, trimazosin, yohimbine, phenoxybenzamine, phentolamine, bunazosin, urapidil, alfuzosin, ketanserin, monatepil, SUN 9221, S-2150, apraclonidine, guanfacil, rilmenidine, and moxonidine.
A pharmaceutical composition for the treatment or prevention of a cardiovascular disorder comprising a first amount of an aldosterone receptor antagonist, a second amount of an alpha-adrenergic modulating agent, and one or more pharmaceutically acceptable carrier materials, wherein said first amount and said second amount together comprise a therapeutically-effective amount of said aldosterone receptor antagonist and said alpha-adrenergic modulating agent, and wherein said composition exhibits a release profile, determined using a suitable release profile test, in which more than about 20% by weight of the aldosterone receptor antagonist is released from the composition at about four hours after initiation of the test.
A method for the treatment or prevention of a cardiovascular disorder in a subject susceptible to or afflicted with such disorder comprising administering to the subject a first amount of an aldosterone receptor antagonist and:
The method of claim 86 wherein said 20-spiroxane compound is characterized by the presence of a 9α-,11α-substituted epoxy moiety.
A kit for the treatment or prevention of a cardiovascular disorder comprising an aldosterone receptor antagonist and an alpha-adrenergic modulating agent.
Dependencies are inferred from the claim text.