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Method to inhibit restenosis

Assignee: Novelion Therapeutics Inc
•
Filing: 1993-07-29
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Granted: 1995-06-06
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Expires: 2013-07-29
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Abstract

Abstract A method to inhibit the development of intimal hyperplasia following vascular intervention procedures (angioplasty) is disclosed. The method consists essentially of administering a green porphyrin to the subject concurrent with and following the angioplasty. No purposeful irradiation with light absorbed by the green porphyrin is required or employed in the method.

Inventors

  • 👤 G. Michael Vincent
  • 👤 Patricia M. Logan

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 19:34
CPC Classifications
A; A61; A61K; A61K31/00; A61K31/33; A61K31/395; A61K31/40; A61P; A61P9/00; A61P9/08

Claims Analysis

Total Claims: 24
Claim 1
Independent Claim 51 words
A method to inhibit the development of intimal hyperplasia following angioplasty which method comprises administering to a subject in conjunction with said angioplasty an amount of green porphyrin (Gp) effective to inhibit said development, and allowing said inhibition to occur in the absence of irradiation with light absorbed by said Gp.
Claim 2
Independent Claim 51 words
A method to inhibit the development of intimal hyperplasia following angioplasty which method comprises administering to a subject in conjunction with said angioplasty an amount of green porphyrin (Gp) effective to inhibit said development, and allowing said inhibition to occur in the absence of irradiation with light absorbed by said Gp.
Claim 3
Dependent Claim 27 words
The method of claim 1 wherein said administering is conducted by administering 2-5 doses, wherein the first said dose is administered within 6 hours of said angioplasty.
Claim 4
Dependent Claim 15 words
The method of claim 2 wherein said effective amount is 0.01-5 mg/kg in each dose.
Claim 5
Dependent Claim 15 words
The method of claim 3 wherein said effective amount is 0.05-2 mg/kg in each dose.
Claim 6
Dependent Claim 14 words
The method of claim 1 wherein said Gp is administered in a liposomal formulation.
Claim 7
Dependent Claim 32 words
The method of claim 1 wherein Gp is of the formula 1-6, as shown in FIG. 1, wherein R 1 , R 2 , R 3 and R 4 are non-interfering substituents.
Claim 8
Dependent Claim 15 words
The method of claim 6 wherein R 1 and R 2 are carbomethoxy and carboethoxy.
Claim 9
Dependent Claim 24 words
The method of claim 6 wherein each R 3 is --CH 2 CH 2 COOH or a salt, amide, ester or acyl hydrazone thereof.
Claim 10
Dependent Claim 21 words
The method of claim 6 wherein Gp is of the formula 3 or 4, wherein R 4 is a non-interfering substituent.
Claim 11
Dependent Claim 20 words
The method of claim 9 wherein said Gp is selected from the group consisting of BPD-DA, BPD-DB, BPD-MA and BPD-MB.
Claim 12
Dependent Claim 10 words
The method of claim 10 wherein said Gp is BPD-MA.
Claim 13
Independent Claim 53 words
A method to inhibit the development of intimal hyperplasia following angioplasty which method consists essentially of administering to a subject in conjunction with said angioplasty an amount of green porphyrin (Gp) effective to inhibit said development, and allowing said inhibition to occur in the absence of irradiation with light absorbed by said Gp.
Claim 14
Independent Claim 53 words
A method to inhibit the development of intimal hyperplasia following angioplasty which method consists essentially of administering to a subject in conjunction with said angioplasty an amount of green porphyrin (Gp) effective to inhibit said development, and allowing said inhibition to occur in the absence of irradiation with light absorbed by said Gp.
Claim 15
Dependent Claim 27 words
The method of claim 12 wherein said administering is conducted by administering 2-5 doses, wherein the first said dose is administered within 6 hours of said angioplasty.
Claim 16
Dependent Claim 15 words
The method of claim 13 wherein said effective amount is 0.01-5 mg/kg in each dose.
Claim 17
Dependent Claim 15 words
The method of claim 14 wherein said effective amount is 0.05-2 mg/kg in each dose.
Claim 18
Dependent Claim 14 words
The method of claim 12 wherein said Gp is administered in a liposomal formulation.
Claim 19
Dependent Claim 32 words
The method of claim 12 wherein Gp is of the formula 1-6, as shown in FIG. 1, wherein R 1 , R 2 , R 3 and R 4 are non-interfering substituents.
Claim 20
Dependent Claim 15 words
The method of claim 17 wherein R 1 and R 2 are carbomethoxy and carboethoxy.
Claim 21
Dependent Claim 24 words
The method of claim 17 wherein each R 3 is --CH 2 CH 2 COOH or a salt, amide, ester or acyl hydrazone thereof.
Claim 22
Dependent Claim 21 words
The method of claim 17 wherein Gp is of the formula 3 or 4, wherein R 4 is a non-interfering substituent.
Claim 23
Dependent Claim 20 words
The method of claim 20 wherein said Gp is selected from the group consisting of BPD-DA, BPD-DB, BPD-MA and BPD-MB.
Claim 24
Dependent Claim 10 words
The method of claim 21 wherein said Gp is BPD-MA.

References Cited (Backward Citations)

US5283255A Cited
US5314905A Cited
US5308608A Cited
US5116864A Cited
US5308861A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1998-06-05 1998-12-05 1999-06-06 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 2002-06-05 2002-12-05 2003-06-06 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2006-06-05 2006-12-05 2007-06-06 $7700.00 Window Closed / Lapsed

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