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US3965254A Expired / Lapsed US ⏱️ 0.0 years remaining

Compositions for the treatment of calcific tumors

Assignee: Procter and Gamble Co
•
Filing: 1974-11-15
•
Granted: 1976-06-22
•
Expires: 1994-11-15
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Abstract

Abstract Composition in unit dosage form comprising mono-, di- and polyphosphonate compounds having therapeutic levels of radioactive phosphorus (as 32 P and 33 P) incorporated therein are disclosed. Due to the extremely high affinity of the polyphosphonate compounds for active bone tumors and their exceptionally low retention in soft tissue they are ideal for therapy of both primary and metastatic bone tumors and soft tissue tumors which calcify.

Inventors

  • 👤 Andrew John Tofe
  • 👤 Marion David Francis

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-25 22:27
CPC Classifications
A; A61; A61K; A61K51/00; A61K51/02; A61K51/04; A61K51/0489; A61K2121/00

Claims Analysis

Total Claims: 18
Claim 1
Independent Claim 210 words
A sterile dilute composition in unit dosage form comprising from about 2 to 20 millicuries of a 32 P or 33 P tagged polyphosphonate compound suitable for the treatment of calcific tumors selected from the group consisting of: ##EQU9## wherein each R is hydrogen or CH 2 OH and n is an integer of from 3 to 10; ##EQU10## wherein R 1 is hydrogen, alkyl containing from 1 to about 20 carbon atoms, alkenyl containing from 2 to about 20 carbon atoms, aryl, phenylethenyl, benzyl, halogen, hydroxyl, amino, substituted amino, --CH 2 COOH, --CH 2 PO 3 H 2 , --CH(PO 3 H 2 ) (OH), or -CH 2 C(PO 3 H 2 ) 2n -H where n is 1 to 15, R 2 is hydrogen, lower alkyl, amino benzyl, halogen, hydroxyl, --CH 2 COOH, --CH 2 PO 3 H 2 , or --CH 2 Ch 2 PO 3 H 2; ##EQU11## wherein n is an integer of from 3 to 9; ##EQU12## wherein each R 3 is hydrogen or lower alkyl (e.g., methyl, ethyl, propyl and butyl); ##EQU13## wherein n is an integer of from 2 to 4; ##EQU14## wherein X and Y are each hydrogen or hydroxy; and the pharmaceutically acceptable salts of each of the foregoing acids.
Claim 2
Dependent Claim 210 words
A sterile dilute composition in unit dosage form comprising from about 2 to 20 millicuries of a 32 P or 33 P tagged polyphosphonate compound suitable for the treatment of calcific tumors selected from the group consisting of: ##EQU9## wherein each R is hydrogen or CH 2 OH and n is an integer of from 3 to 10; ##EQU10## wherein R 1 is hydrogen, alkyl containing from 1 to about 20 carbon atoms, alkenyl containing from 2 to about 20 carbon atoms, aryl, phenylethenyl, benzyl, halogen, hydroxyl, amino, substituted amino, --CH 2 COOH, --CH 2 PO 3 H 2 , --CH(PO 3 H 2 ) (OH), or -CH 2 C(PO 3 H 2 ) 2n -H where n is 1 to 15, R 2 is hydrogen, lower alkyl, amino benzyl, halogen, hydroxyl, --CH 2 COOH, --CH 2 PO 3 H 2 , or --CH 2 Ch 2 PO 3 H 2; ##EQU11## wherein n is an integer of from 3 to 9; ##EQU12## wherein each R 3 is hydrogen or lower alkyl (e.g., methyl, ethyl, propyl and butyl); ##EQU13## wherein n is an integer of from 2 to 4; ##EQU14## wherein X and Y are each hydrogen or hydroxy; and the pharmaceutically acceptable salts of each of the foregoing acids.
Claim 3
Dependent Claim 17 words
The composition of Claim 1 wherein the polyphosphonate is ethane-1-hydroxy-1,1-diphosphonic acid or a pharmaceutically acceptable salt thereof.
Claim 4
Dependent Claim 16 words
The composition of Claim 1 wherein the polyphosphonate is dichloromethanediphosphonic acid or a pharmaceutically acceptable salt.
Claim 5
Dependent Claim 17 words
The composition of claim 1 wherein the polyphosphonate is tris (phosphonomethyl)amine or a pharmaceutically acceptable salt thereof.
Claim 6
Dependent Claim 17 words
The composition of claim 1 wherein the polyphosphonate is methanecyclohexylhydroxydiphosphonic acid or a pharmaceutically acceptable salt thereof.
Claim 7
Dependent Claim 16 words
The composition of claim 1 wherein the polyphosphonate is 3,3,4,4,5,5-hexafluoro-1,2-diphosphonocyclopent-1-ene or a pharmaceutically acceptable salt thereof.
Claim 8
Dependent Claim 18 words
The composition of claim 1 wherein the polyphosphonate is cyclic tetraphosphonic acid or a pharmaceutically acceptable salt thereof.
Claim 9
Dependent Claim 17 words
The composition of claim 1 wherein the polyphosphonate is ethene-1,2-dicarboxy-1-phosphonic acid or a pharmaceutically acceptable salt thereof.
Claim 10
Dependent Claim 17 words
The composition of claim 1 wherein the polyphosphonate is ethane-1,2-dicarboxy-1,2-diphosphonic acid or a pharmaceutically acceptable salt thereof.
Claim 11
Independent Claim 209 words
A method for the treatment of calcific tumors comprising systemically administering to an animal afflicted therewith a safe but effective dose of a radioactive compound tagged with 32 P or 33 P selected from the group consisting of: ##EQU15## wherein each R is hydrogen or CH 2 OH or CH 2 OH and n is an integer of from 3 to 10, ##EQU16## wherein R 1 is hydrogen, alkyl containing from 1 to about 20 carbon atoms, alkenyl containing from 2 to about 20 carbon atoms, aryl, phenylethenyl, benzyl, halogen, hydroxyl, amino, substituted amino, --CH 2 COOH, --CH 2 PO 3 H 2 , -CH(PO 3 H 2 ) (OH), or --[CH 2 C(PO 3 H 2 ] n -H, where n is 1 to 15, R 2 is hydrogen, lower alkyl, amino, benzyl, halogen, hydroxyl, --CH 2 COOH, --CH 2 PO 3 H 2 , or --CH 2 Ch 2 PO 3 H 2; ##EQU17## wherein n is an integer of from 3 to 9, ##EQU18## wherein each R 3 is hydrogen or lower alkyl (e.g., methyl, ethyl, propyl and butyl); ##EQU19## wherein n is an integer of from 2 to 4; ##EQU20## wherein X and Y are each hydrogen or hydroxy; and the pharmaceutically acceptable salts thereof.
Claim 12
Independent Claim 209 words
A method for the treatment of calcific tumors comprising systemically administering to an animal afflicted therewith a safe but effective dose of a radioactive compound tagged with 32 P or 33 P selected from the group consisting of: ##EQU15## wherein each R is hydrogen or CH 2 OH or CH 2 OH and n is an integer of from 3 to 10, ##EQU16## wherein R 1 is hydrogen, alkyl containing from 1 to about 20 carbon atoms, alkenyl containing from 2 to about 20 carbon atoms, aryl, phenylethenyl, benzyl, halogen, hydroxyl, amino, substituted amino, --CH 2 COOH, --CH 2 PO 3 H 2 , -CH(PO 3 H 2 ) (OH), or --[CH 2 C(PO 3 H 2 ] n -H, where n is 1 to 15, R 2 is hydrogen, lower alkyl, amino, benzyl, halogen, hydroxyl, --CH 2 COOH, --CH 2 PO 3 H 2 , or --CH 2 Ch 2 PO 3 H 2; ##EQU17## wherein n is an integer of from 3 to 9, ##EQU18## wherein each R 3 is hydrogen or lower alkyl (e.g., methyl, ethyl, propyl and butyl); ##EQU19## wherein n is an integer of from 2 to 4; ##EQU20## wherein X and Y are each hydrogen or hydroxy; and the pharmaceutically acceptable salts thereof.
Claim 13
Dependent Claim 17 words
The method of claim 10 wherein said compound is ethane-1-hydroxy-1,1-diphosphonic acid or a pharmaceutically acceptable salt thereof.
Claim 14
Dependent Claim 17 words
The method of claim 10 wherein said compound is dichloromethanediphosphonic acid or a pharmaceutically acceptable salt thereof.
Claim 15
Independent Claim 232 words
A method for the treatment of calcific tumors comprising systemically administering to an animal affected therewith a safe but effective dose of a radioactive compound tagged with 32 P or 33 P selected from the group consisting of: ##EQU21## wherein each R is hydrogen or CH 2 OH and n is an integer of from 3 to 10; ##EQU22## wherein R 1 is hydrogen, alkyl containing from 1 to about 20 carbon atoms, alkenyl containing from 2 to about 20 carbon atoms, aryl, phenylethenyl, benzyl, halogen, hydroxyl, amino, substituted amino, --CH 2 COOH, --CH 2 COOH, --CH 2 PO 3 H 2 , --CH(PO 3 H 2 ) (OH), or -[CH 2 C(PO 3 H 2 ) 2 ] n -H, where n is 1 to 15, R 2 is hydrogen, lower alkyl, amino, benzyl, halogen, hydroxyl, --CH 2 COOH, --CH 2 PO 3 H 2 , or CH 2 CH 2 PO 3 H 2; ##EQU23## wherein n is an integer of from 3 to 9; ##EQU24## wherein each R 3 is hydrogen or lower alkyl (e.g., methyl, ethyl, propyl and butyl); ##EQU25## wherein nis an integer of from 2 to 4; ##EQU26## wherein X and Y are each hydrogen or hydroxy; and the pharmaceutically acceptable salts thereof; and subsequently administering a chemotherapeutic agent selected from the group consisting of: alkylating agents; antimetabolites; antibiotics; vinca alkaloids; hormones; enzymes; hydroxyurea; and procabazine.
Claim 16
Independent Claim 232 words
A method for the treatment of calcific tumors comprising systemically administering to an animal affected therewith a safe but effective dose of a radioactive compound tagged with 32 P or 33 P selected from the group consisting of: ##EQU21## wherein each R is hydrogen or CH 2 OH and n is an integer of from 3 to 10; ##EQU22## wherein R 1 is hydrogen, alkyl containing from 1 to about 20 carbon atoms, alkenyl containing from 2 to about 20 carbon atoms, aryl, phenylethenyl, benzyl, halogen, hydroxyl, amino, substituted amino, --CH 2 COOH, --CH 2 COOH, --CH 2 PO 3 H 2 , --CH(PO 3 H 2 ) (OH), or -[CH 2 C(PO 3 H 2 ) 2 ] n -H, where n is 1 to 15, R 2 is hydrogen, lower alkyl, amino, benzyl, halogen, hydroxyl, --CH 2 COOH, --CH 2 PO 3 H 2 , or CH 2 CH 2 PO 3 H 2; ##EQU23## wherein n is an integer of from 3 to 9; ##EQU24## wherein each R 3 is hydrogen or lower alkyl (e.g., methyl, ethyl, propyl and butyl); ##EQU25## wherein nis an integer of from 2 to 4; ##EQU26## wherein X and Y are each hydrogen or hydroxy; and the pharmaceutically acceptable salts thereof; and subsequently administering a chemotherapeutic agent selected from the group consisting of: alkylating agents; antimetabolites; antibiotics; vinca alkaloids; hormones; enzymes; hydroxyurea; and procabazine.
Claim 17
Dependent Claim 17 words
The method of claim 13 wherein said compound is ethane-1-hydroxy-1,1-diphosphonic acid or a pharmaceutically acceptable salt thereof.
Claim 18
Dependent Claim 17 words
The method of claim 13 wherein said compound is dichloromethanediphosphonic acid or a pharmaceutically acceptable salt thereof.

References Cited (Backward Citations)

US3213129A Cited
US3336221A Cited
US3387024A Cited
US3400151A Cited
US3532639A Cited
US3553314A Cited
US3553315A Cited
US3579570A Cited
US3743688A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1979-06-22 1979-12-22 1980-06-22 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1983-06-22 1983-12-22 1984-06-22 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1987-06-22 1987-12-22 1988-06-22 $7700.00 Window Closed / Lapsed

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