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US5978698A Expired / Lapsed US ⏱️ 0.0 years remaining

Angioplasty procedure using nonionic contrast media

Assignee: Medicure International Inc
•
Filing: 1997-10-08
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Granted: 1999-11-02
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Expires: 2017-10-08
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Abstract

Abstract A method for treating patients in need of percutaneous transluminal coronary angioplasty which comprises administering nonionic contract media to the patient and treating the patient with a fibrinogen receptor antagonist.

Inventors

  • 👤 Frederic L. Sax

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 17:16
CPC Classifications
A; A61; A61K; A61K49/00; A61K49/001; A61K49/0013; A61K49/0017

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 95 words
A method for treating a patient having coronary artery blockage which comprises a) introducing nonionic contrast dye into the coronary artery having blockage to image the blockage, b) administering a fibrinogen receptor antagonist to the patient, and inserting a balloon catheter into the blockage and inflating the balloon at the location of the blockage to revascularize the artery, and c) administering fibrinogen receptor antagonist to the patient following balloon inflation wherein the fibrinogen receptor antagonist is administered in a therapeutically effective amount sufficient to provide at least 70% inhibition of fibrinogen binding to GP IIb/IIIa.
Claim 2
Independent Claim 95 words
A method for treating a patient having coronary artery blockage which comprises a) introducing nonionic contrast dye into the coronary artery having blockage to image the blockage, b) administering a fibrinogen receptor antagonist to the patient, and inserting a balloon catheter into the blockage and inflating the balloon at the location of the blockage to revascularize the artery, and c) administering fibrinogen receptor antagonist to the patient following balloon inflation wherein the fibrinogen receptor antagonist is administered in a therapeutically effective amount sufficient to provide at least 70% inhibition of fibrinogen binding to GP IIb/IIIa.
Claim 3
Dependent Claim 29 words
A method of claim 1 wherein the fibrinogen receptor antagonist is administered to the patient according to step c) for a period of time of at least 24 hours.
Claim 4
Dependent Claim 13 words
A method of claim 1 wherein the fibrinogen receptor antagonist is orally administered.
Claim 5
Dependent Claim 31 words
A method of claim 3, wherein the fibrinogen receptor antagonist is selected from the group consisting of 2(S)-[(p-Toluenesulfonyl)amino]-3-[[[5,6,7,8-tetrahydro-4-oxo-5-[2-(piperidin-4-yl)ethyl]-4H-pyrazolo-[1,5-a][1,4]diazepin-2-yl]carbonyl]-amino]propionic acid, Methyl-N 3 -[2-{3-(4-formamidinophenyl)-isoxazolin-5(R)-yl}-acetyl]-N 2 -(n-butyloxycarbonyl)-2,3-(S)-diaminopropionate acetate salt, Ethyl 3-[[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentynoate, and, (R)-methyl-3-[[[3-[4-(aminoiminomethyl)phenyl]-4,5-dihydro-5-isoxazolyl]acetyl]amino]-N-(butoxycarbonyl)-L-alanine monoacetate.
Claim 6
Dependent Claim 13 words
A method of claim 1 wherein the fibrinogen receptor antagonist is intravenously administered.
Claim 7
Dependent Claim 37 words
A method of claim 5, wherein the fibrinogen receptor antagonist is selected from the group consisting of Mpr-(Acetimidyl-Lys)-Gly-Asp-Trp-Phe-Cys-NH 2 , Mpr-(Acetimidyl-Lys)-Gly-Asp-Trp-Phe-Pen-NH 2 , Mpr-(Phenylimidyl-Lys)-Gly-Asp-Trp-Phe-Pen-NH 2 , Mpr-(Phenylimidyl-Lys)-Gly-Asp-Trp-Phe-Cys-NH 2 , N-Methyl-D-phenylalanyl-N-[(1S)-1-formyl-4-guanidinobutyl]-L-prolinamide, ((1-(2-((4-(aminoiminomethyl)benzoyl)amino)-3-(4-hydroxyphenyl)-1-oxopropyl)-4-piperidinyl)oxy)-(S)-acetic acid, N-(2-(2-(((3-((aminoiminomethyl)amino)propyl)amino)carbonyl)-1-piperidnyl)-1-(cyclohexylmethyl)-2-oxoethyl)-(R,S)-glycine, and (2-S-(n-Butylsulfonylamino)-3[4-(piperidin-4-yl)butyloxyphenyl]propionic acid hydrochloride.
Claim 8
Dependent Claim 14 words
A method of claim 5 wherein the fibrinogen receptor antagonist is Mpr-(Har)-G-D-W-P-C-NH 2 .

References Cited (Backward Citations)

US5292756A Cited
US5281585A Cited

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