US2004138306A1PendingUtilityA1
Use of a specific cyclic amine derivative or the pharmaceutically acceptable salts thereof for the treatment or prevention of heart failure
Assignee: BOEHRINGER INGELHEIM PHARMAPriority: Jul 25, 2002Filed: Jul 24, 2003Published: Jul 15, 2004
Est. expiryJul 25, 2022(expired)· nominal 20-yr term from priority
A61K 9/0095A61K 31/195A61K 45/06A61K 31/55A61P 9/00
61
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present invention provides the use in a pharmaceutical composition of a specific cyclic amine derivative, or its pharmaceutically acceptable salts, for the treatment or prevention of heart failure of any aetiology.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for the treatment or prevention of heart failure, which comprises the administration to a patient in need thereof of a pharmaceutical composition comprising cilobradine or a pharmaceutically acceptable salt thereof, together with a pharmaceutically suitable carrier.
2 . The method of claim 1 for the prevention of heart failure.
3 . The method of claim 1 for the treatment of heart failure.
4 . The method of claim 1 wherein the galenical formulation of the pharmaceutical composition is a tablet, a drinking solution, a capsule, a suppository or an injectable formulation.
5 . The method of claim 4 wherein the galenical formulation of the pharmaceutical composition is a tablet.
6 . The method of claim 4 wherein the galenical formulation of the pharmaceutical composition is a drinking solution.
7 . The method of claim 1 wherein the pharmaceutical composition is administered following a single or multiple stage daily application scheme.
8 . The method of claim 7 wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.01 and 20 mg/kg body weight.
9 . The method of claim 7 wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.05 and 5 mg/kg body weight.
10 . The method of claim 7 wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.1 and 2.5 mg/kg body weight.
11 . The method according to claim 7 wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.1 and 1 mg/kg body weight.
12 . The method of claim 7 wherein the administered dose of cilobradine or its pharmaceutically acceptable salt is between 0.1 and 0.75 mg/kg body weight.
13 . The method of claim 1 wherein the treatment or prevention of heart failure is performed in combination with other therapeutic agents for the treatment or prevention of heart failure.
14 . The method of claim 13 wherein said therapuuetic agents include diuretics, cardiac glycosides, ACE inhibitors, ARBs, vasodilators, beta blockers or inotropes.Join the waitlist — get patent alerts
Track US2004138306A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.