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US5133956A Expired / Lapsed US ⏱️ 0.0 years remaining

Radiolabeled metal-binding protein for the treatment of arthritis

Assignee: Mallinckrodt Inc
•
Filing: 1991-05-30
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Granted: 1992-07-28
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Expires: 2011-05-30
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Abstract

Abstract Radioactive high molecular weight metal-binding protein compositions and a method for therapeutic radiation treatment including the treatment of rheumatoid arthritis comprising injection of a radioactive high molecular weight metal-binding protein compositions are disclosed.

Inventors

  • 👤 Joseph R. Garlich
  • 👤 Kenneth McMillan
  • 👤 Jaime Simon

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 02:36
CPC Classifications
A; A61; A61K; A61K51/00; A61K51/02; A61K51/04; A61K51/08; A61K51/088; A61P; A61P19/00; A61P19/02; A61P29/00; C; C07; C07B; C07B59/00; C07B59/008; A61K2121/00

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 67 words
A method for the treatment of rheumatoid arthritis comprising injecting into the synovium of a subject in need of such treatment a therapeutically effective amount of a pharmaceutical composition comprising a metal-binding protein having a molecular weight of approximately greater than 50,000 and a therapeutic radionuclide bound to the protein, wherein the radionuclide is a beta-emitter with a half-life from about 2 hours to about 7 days.
Claim 2
Independent Claim 67 words
A method for the treatment of rheumatoid arthritis comprising injecting into the synovium of a subject in need of such treatment a therapeutically effective amount of a pharmaceutical composition comprising a metal-binding protein having a molecular weight of approximately greater than 50,000 and a therapeutic radionuclide bound to the protein, wherein the radionuclide is a beta-emitter with a half-life from about 2 hours to about 7 days.
Claim 3
Independent Claim 75 words
A method for the treatment of rheumatoid arthritis comprising injecting into the synovium of a subject in need of such treatment a therapeutically effective amount of a pharmaceutical composition comprising a protein having a molecular weight of approximately greater than 50,000, a bifunctional chelator covalently attached to the protein, and a therapeutic radionuclide chelated to the bifunctional chelator, wherein the radionuclide is a beta-emitter having a half-life of about 2 hours to about 7 days.
Claim 4
Independent Claim 75 words
A method for the treatment of rheumatoid arthritis comprising injecting into the synovium of a subject in need of such treatment a therapeutically effective amount of a pharmaceutical composition comprising a protein having a molecular weight of approximately greater than 50,000, a bifunctional chelator covalently attached to the protein, and a therapeutic radionuclide chelated to the bifunctional chelator, wherein the radionuclide is a beta-emitter having a half-life of about 2 hours to about 7 days.
Claim 5
Dependent Claim 17 words
The method of claim 1, wherein the protein has a molecular weight of approximately greater than 250,000.
Claim 6
Dependent Claim 10 words
The method of claim 3 wherein the protein is ferritin.
Claim 7
Dependent Claim 10 words
The method of claim 2 wherein the protein is transferrin.
Claim 8
Dependent Claim 16 words
The method of claim 2, wherein the bifunctional chelator contains a polyaminocarboxylate or polyaminophosphonate chelating moiety.
Claim 9
Dependent Claim 31 words
The method of claim 6 wherein the bifunctional chelator is selected from the group consisting of 1,3-propanediamine-N-(carboxy-propyl)-N,N',N'-trimethylenephosphonic acid, ethylenediamine-N-(4-aminophenethyl)-N,N',N',-trimethylenephosphonic acid, ethylenediaminetetramethylenephosphonic acid, 1-(carboxy)ethylenediaminetetramethylenephosphonic acid, 1-(4-aminobenzyl)ethylenediaminetetramethylenephosphonic acid, N"-(4-aminophenyl)-dipropylenetriamine-N',N',N'",N'"-tetramethylenephosphonic acid and N"-(4-aminophenethyl)-diethylenetriamine-N'N',N'",N'"-tetramethylenephosphonic acid.
Claim 10
Dependent Claim 17 words
The method of claim 6, wherein the bifunctional chelator contains a cyclic polyaminocarboxylate or polyaminophosphonate chelating moiety.
Claim 11
Dependent Claim 45 words
The method of claim 8, wherein the bifunctional chelator is selected from the group consisting of α-aminophenyl-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid, substituted 1,4,7-tris-carboxymethyl-1,4,7,10-tetraazacyclododecane, 1,4,8,11-tetraazacyclotetra-decane-N,N',N",N'"-tetraacetic acid, 2-(p-nitrobenzyl)-1,4,7,10-tetraazacyclododecane-N,N',N",N'"-tetraacetic acid, α-[2-(4-aminophenyl)ethyl]-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid, α-[2-(4-aminophenyl)ethyl]-1,4,7,10-tetraazacyclododecane-1-acetic-4,7,10-tris(methylacetic acid, α-(4-aminophenyl)-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid, α-(5-amino-2-methoxyphenyl)-1,4,7,10-tetraazacylododecnae-1,4,7,10-tetraacetic acid, 1-[2-(4-aminophenyl)ethyl]-1,4,7,10-tetraazacyclododecnae-4,7,10-triacetic acid, 1,4,7,10-tetraazacyclododecane-N,N',N",N'"-tetraacetic acid, 1,4,7,10-tetraazacyclotridecane-N,N'N",N'"-tetraacetic acid, 1,4,8,11-tetraazacyclotetradecane-N,N'N",N'"-tetraacetic acid, 1,5,9,13-tetraazacyclohexadecane-N,N'N",N'"-tetraacetic acid, and 1,4,7,10-tetraazacyclododenace-1,4,7,10-tetramethylenephosphonic acid.
Claim 12
Dependent Claim 12 words
The method of claim 9 wherein the bifunctional chelator is α-aminophenyl-1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid.
Claim 13
Dependent Claim 12 words
The method of claim 9 wherein the bifunctional chelator is α-[2-(4-aminophenyl)ethyl]-1,4,7,10-tetraazacyclododecane-1-acetic-4,7,10-tris(methylacetic acid).
Claim 14
Dependent Claim 17 words
The method of claim 2, wherein the protein has a molecular weight of approximately greater than 250,000.
Claim 15
Dependent Claim 26 words
The method of claim 1, wherein said radionuclide is selected from the group consisting of Ho-166, Sm-153, Re-186, Rh-105, Lu-177, In-115 m, Dy-165, Sc-47 and Re-188.
Claim 16
Dependent Claim 26 words
The method of claim 2, wherein said radionuclide is selected from the group consisting of Ho-166, Sm-153, Re-186, Rh-105, Lu-177, In-115 m, Dy-165, Sc-47 and Re-188.
Claim 17
Dependent Claim 12 words
The method of claim 13, wherein said radionuclide is Sm-153 or Ho-166.
Claim 18
Dependent Claim 12 words
The method of claim 14, wherein said radionuclide is Sm-153 or Ho-166.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1995-07-28 1996-01-27 1996-07-28 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1999-07-28 2000-01-27 2000-07-28 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 2003-07-28 2004-01-27 2004-07-28 $7700.00 Window Closed / Lapsed

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