IP Library Granted Patent US 7,125,889
Granted Patent B2
US 7,125,889 · App. 10/639,949 · Granted Oct 24, 2006

Treating of cardiovascular and related pathologies

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,125,889
App. No.
10/639,949
Granted
Oct 24, 2006
Kind
B2
Abstract

Methods for treating cardiovascular and related diseases such as blood clots are described. The methods are directed to concurrently administering a compound such as pyridoxal-5′-phosphate, pyridoxamine, pyridoxal, or a 3-acylated pyridoxal analogue with a therapeutic cardiovascular compound.

Claims (14)

1. A method of reducing blood clots in a mammal comprising: concurrently administering to the mammal a therapeutically effective amount for reducing blood clots of a combination of a compound selected from the group consisting of pyridoxal-5′-phosphate, pyridoxal, pyridoxamine, a 3-acylated pyridoxal analogue, a pharmaceutically acceptable acid addition salt thereof, and a mixture thereof, and a cardiovascular compound selected from the group consisting of pyridoxal phophate-6-azophenyl-2′,4′-disulphonic acid (PPADS) and an anti-thrombotic agent, wherein the 3-acylated pyridoxal analogue is a compound of the formula

wherein

R 1 is a straight or branched alkyl group, a straight or branched alkenyl group, in which an alkyl or alkenyl group may be interrupted by a nitrogen or oxygen atom; an alkoxy group; a dialkylamino group; or an unsubstituted or substituted aryl group; and

R 2 is a secondary amino group.

2. A method according to claim 1 , wherein the 3-acylated pyridoxal analogue is a compound of the formula

wherein

R 1 is a straight or branched alkyl group, a straight or branched alkenyl group, in which an alkyl or alkenyl group may be interrupted by a nitrogen or oxygen atom; an alkoxy group; a dialkylamino group; or an unsubstituted or substituted aryl group.

3. A method according to claim 1 , wherein the 3-acylated pyridoxal analogue is a compound of the formula

wherein

R 1 is a straight or branched alkyl group, a straight or branched alkenyl group, in which an alkyl or alkenyl group may be interrupted by a nitrogen or oxygen atom; an alkoxy group; a dialkylamino group; or an unsubstituted or substituted aryl group; and

R 2 is a secondary amino group.

4. A method according to claim 1 , wherein the anti-thrombotic agent is an antiplatelet agent, aspirin, or heparin.

5. A method according to claim 1 , wherein the compound is administered enterally or parenterally and the anti-thrombotic agent is administered enterally or parenterally.

6. A method according to claim 1 , wherein the compound and the anti-thrombotic agent are administered in a single dosage form.

Assignments (1)
RELEASE OF SECURITY INTEREST Recorded Jul 26, 2011
From: BIRMINGHAM ASSOCIATES LTD.
To: MEDICURE INTERNATIONAL INC.
Reel/Frame 026653/0168 →