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US5385935A Expired / Lapsed US ⏱️ 0.0 years remaining

Method for the inhibition of restenosis associated with coronary intervention

Assignee: Kissei Pharmaceutical Co Ltd
•
Filing: 1993-09-07
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Granted: 1995-01-31
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Expires: 2013-09-07
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Abstract

Abstract This invention provides a method for treating patients to inhibit restenosis associated with coronary intervention. A 600 mg dosage of Tranilast for a treatment period of three consecutive months after coronary intervention lowers the incidence of restenosis, and reduces the degree of stenosis in patients.

Inventors

  • 👤 Hideo Tamai
  • 👤 Kinzo Ueda
  • 👤 Yung-sheng Hsu

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 14:10
CPC Classifications
A; A61; A61K; A61K31/00; A61K31/185; A61K31/19; A61P; A61P43/00; A61P9/00; A61P9/10

Claims Analysis

Total Claims: 9
Claim 1
Independent Claim 49 words
A method for the inhibition restenosis associated with coronary intervention in a human patient, which comprises administering to the patient 2-(3,4-dimethoxycinnamoyl)aminobenzoic acid or a pharmaceutically acceptable salt thereof in a daily dose of about 300-1000 mg for a treatment period of at least three consecutive months after coronary intervention.
Claim 2
Independent Claim 49 words
A method for the inhibition restenosis associated with coronary intervention in a human patient, which comprises administering to the patient 2-(3,4-dimethoxycinnamoyl)aminobenzoic acid or a pharmaceutically acceptable salt thereof in a daily dose of about 300-1000 mg for a treatment period of at least three consecutive months after coronary intervention.
Claim 3
Dependent Claim 24 words
A method in accordance with claim 1 wherein the dosage is between about 300-600 mg of 2-(3,4-dimethoxycinnamoyl)aminobenzoic acid or a pharmaceutically acceptable salt thereof.
Claim 4
Dependent Claim 20 words
A method in accordance with claim 1 wherein the treatment period is between about 3-6 consecutive months after coronary intervention.
Claim 5
Dependent Claim 13 words
A method in accordance with claim 1 wherein the dosage is administered orally.
Claim 6
Dependent Claim 13 words
A method in accordance with claim 1 wherein the dosage is administered parenterally.
Claim 7
Dependent Claim 16 words
A method in accordance with claim 1 wherein the coronary intervention is Percutaneous Transluminal Coronary Angioplasty.
Claim 8
Dependent Claim 15 words
A method in accordance with claim 1 wherein the coronary intervention is Direction Coronary Atherectomy.
Claim 9
Dependent Claim 13 words
A method in accordance with claim 1 wherein the coronary intervention is Stent.

References Cited (Backward Citations)

US3940422A Cited
US4070484A Cited
US4337270A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1998-01-30 1998-08-01 1999-01-31 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2002-01-30 2002-08-01 2003-01-31 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2006-01-30 2006-08-01 2007-01-31 $7700.00 Window Closed / Lapsed

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