IP Library Granted Patent US 8,057,815
Granted Patent B2
US 8,057,815 · App. 11/107,324 · Granted Nov 15, 2011

Methods of treatment with Syk inhibitors

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Quick Facts
Patent No.
US 8,057,815
App. No.
11/107,324
Granted
Nov 15, 2011
Kind
B2
Abstract

The present invention provides novel compositions and methods for inhibiting restenosis, thrombosis, and/or inflammation in a patient undergoing a vascular intervention. More particularly, the present invention provides intravascular devices coated with one or more spleen tyrosine kinase (Syk) inhibitors. Methods for inhibiting restenosis, thrombosis, and/or inflammation in a patient by treatment with such intravascular devices are also provided. In addition, the present invention provides methods for treating sickle cell disease using Syk inhibitors.

Claims (13)

1. An intravascular device having a coating, said coating comprising a polymer and a spleen tyrosine kinase (Syk) inhibitor, wherein said Syk inhibitor is selected from the group consisting of a purine-2-benzamine derivative, a pyrimidine-5-carboxamide derivative, a 1,6-naphthyridine derivative, BAY 61-3606, piceatannol, 3,4-dimethyl-10-(3-aminopropyl)-9-acridone oxalate), and combinations thereof; and wherein said coating is applied to said intravascular device, wherein said spleen tyrosine kinase (Syk) inhibitor is present in an amount sufficient to inhibit restenosis, thrombosis, and inflammation in a patient undergoing a vascular intervention.

2. The intravascular device of claim 1 , wherein said intravascular device is selected from the group consisting of a stent, a balloon catheter, an autologous venous/arterial graft, a prosthetic venous/arterial graft, a vascular catheter, and a vascular shunt.

3. The intravascular device of claim 2 , wherein said intravascular device is a stent.

4. The intravascular device of claim 1 , wherein said polymer is selected from the group consisting of a bioabsorbable polymer, a biostable polymer, and combinations thereof.

5. The intravascular device of claim 4 , wherein said bioabsorbable polymer is selected from the group consisting of aliphatic polyesters, poly(amino acids), poly(ether-ester) copolymers, polyalkylene oxalates, polyanhydrides, polysaccharides, polyamides, poly(iminocarbonates), polyorthoesters, polyoxaesters, polyamidoesters, polyoxaesters containing amido groups, polyphosphazenes, and combinations thereof.

6. The intravascular device of claim 4 , wherein said biostable polymer is selected from the group consisting of polyurethanes, silicones, polymethacrylates, poly(ethylene-vinylacetates), polyesters, polyalkyl oxides, polyvinyl alcohols, polyethylene glycols, polyvinyl pyrrolidone, polyolefins, polyisobutylene and ethylene-α-olefin copolymers, acrylic polymers and copolymers, vinyl halide polymers and copolymers, polyvinyl ethers, polyvinylidene halides, polyacrylonitriles, polyvinyl ketones, polyvinyl aromatics, polyvinyl esters, copolymers of vinyl monomers, acrylonitrile-styrene copolymers, acrylonitrile-butadiene-styrene copolymers, ethylene-vinyl acetate copolymers, polyamides, alkyl resins, polycarbonates, polyoxymethylenes, polyimides, polyethers, epoxy resins, rayon, rayon-triacetate, cellulose esters, cellulose acetate, cellulose acetate butyrate, cellophane, cellulose nitrate, cellulose propionate, cellulose ethers, and combinations thereof.

7. The intravascular device of claim 1 , wherein said Syk inhibitor is released from said intravascular device.

8. The intravascular device of claim 1 , wherein said Syk inhibitor is covalently attached to said intravascular device.

9. The intravascular device of claim 1 , wherein said coating contains one or more additional drugs.

10. The intravascular device of claim 9 , wherein said one or more additional drugs are selected from the group consisting of protein kinase inhibitors, antiproliferative agents, antimitotic agents, antibiotics, antimetabolites, pyrimidine analogs, purine analogs, anticoagulants, fibrinolytic agents, antiplatelet agents, antimigratory agents, antisecretory agents, anti-inflammatory agents, non-steroidal agents, immunosuppressive agents, angiogenic agents, and combinations thereof.

11. The intravascular device of claim 10 , wherein said antibiotic is rapamycin.

12. The intravascular device of claim 1 , wherein said coating is applied by dip coating.

13. The intravascular device of claim 1 , wherein said coating is applied by spray coating.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2021
From: PORTOLA PHARMACEUTICALS, LLC
To: ALEXION PHARMACEUTICALS, INC.
Reel/Frame 054999/0218 →
CHANGE OF NAME Recorded Jan 12, 2021
From: PORTOLA PHARMACEUTICALS, INC.
To: PORTOLA PHARMACEUTICALS, LLC
Reel/Frame 054975/0183 →
RELEASE OF SECURITY INTEREST Recorded Jul 2, 2020
From: HCR COLLATERAL MANAGEMENT, LLC
To: PORTOLA PHARMACEUTICALS, INC.
Reel/Frame 053120/0925 →
SECURITY INTEREST Recorded Mar 18, 2019
From: PORTOLA PHARMACEUTICALS, INC.
To: HCR COLLATERAL MANAGEMENT, LLC
Reel/Frame 048633/0673 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 25, 2005
From: ANDRE, PATRICK; PHILIPS, DAVID R.; HOMCY, CHARLES
To: PORTOLA PHARMACEUTICALS, INC.
Reel/Frame 016596/0898 →