IP Library Granted Patent US 7,304,032
Granted Patent B2
US 7,304,032 · App. 11/022,341 · Granted Dec 4, 2007

CD-10 activated prodrug compounds

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Quick Facts
Patent No.
US 7,304,032
App. No.
11/022,341
Granted
Dec 4, 2007
Kind
B2
Abstract

The compounds of the invention are modified forms of therapeutic agents. A typical prodrug compound of the invention comprises a therapeutic agent, an oligopeptide, a stabilizing group and, optionally, a linker group. The prodrug is cleavable by the CD10 enzyme. Methods of treatment using the prodrug and methods of designing a prodrug are also disclosed.

Claims (56)

1. A method for treating a tumor comprising contacting the tumor with a therapeutically effective amount of a CD10 cleavable prodrug, wherein said tumor is comprised of one or more target cells which express CD10 for at least a portion of the target cell life cycle, wherein said tumor is selected from the group consisting of B-cell lymphoma, follicular lymphoma, Burkitt lymphoma, and non-Hodgkins' lymphoma.

2. The method of claim 1 wherein the CD10 cleavable prodrug comprises:

(1) a therapeutic agent capable of entering a target cell,

(2) an oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m ,

wherein:

n and m are integers,

AA P2 represents any amino acid,

AA P1 represents any amino acid,

AA P1′ represents any amino acid, and

each AA independently represents an amino acid,

(3) a stabilizing group, and

(4) optionally, a linker group,

wherein the oligopeptide is directly linked to the stabilizing group at a first attachment site of the oligopeptide and the oligopeptide is directly linked to the therapeutic agent or indirectly linked through the linker group to the therapeutic agent at a second attachment site of the oligopeptide, wherein the stabilizing group hinders cleavage of the prodrug by enzymes present in whole blood.

3. The method of claim 2 wherein n is 0 to 3, m is 0 to 3, and m+n is no more than 3 of the oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m .

4. The method of claim 2 wherein AA P1 of the oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m is selected from the group consisting of arginine, alanine, glycine, leucine, methionine, proline, phenylalanine, tyrosine, glutamine, valine, and serine.

5. The method of claim 2 wherein AA P1′ of the oligopeptide of the formula (AA) n —AA P2 —AA p1 —AA P1′ —(AA) m is selected from the group consisting of leucine, isoleucine, phenylalanine, valine, tyrosine, and proline.

6. The method of claim 2 wherein the prodrug is administered intravenously to a subject having said tumor.

7. The method of claim 2 wherein the prodrug is resistant to cleavage by TOP.

8. The method of claim 2 wherein AA P1 —AA P1′ of the oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m is selected from the group consisting of Arg-Leu, Arg-Ile, Arg-Phe, Arg-Val, Ala-Phe, Ala-Leu, Gly-Phe, Leu-Phe, Leu-Tyr, Met-Leu, Pro-Phe, Pro-Tyr, Pro-Leu, Phe-Leu, Phe-Phe, Tyr-Ile, Tyr-Pro, Tyr-Leu, Gln-Phe, Val-Tyr, Val-Phe, Gly-Trp, Asp-Phe, and Ser-Leu.

9. The method of claim 2 wherein AA 2 of the oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m is a hydrophobic amino acid.

10. The method of claim 2 wherein AA P2 of the oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m is isoleucine.

11. The method of claim 2 wherein the prodrug is selected from the group consisting of Suc-βAla-Leu-Ala-Leu-Dox SEQ ID NO: 41, Suc-Ile-Ala-Leu-Dox SEQ ID NO: 42, Suc-βAla-Ile-Ala-Leu-Dox SEQ ID NO: 39, Suc-Leu-Ala-Leu-Dox SEQ ID NO: 45, and Suc-Met-Ala-Leu-Dox SEQ ID NO: 73.

12. A method for treating a tumor comprising contacting the tumor with a therapeutically effective amount of a CD10 cleavable prodrug, wherein said tumor is comprised of one or more target cells which express CD10 for at least a portion of the target cell life cycle, wherein said tumor is selected from the group consisting of ocular melanoma and cutaneous melanoma.

13. The method of claim 12 wherein the CD10 cleavable prodrug comprises:

(1) a therapeutic agent capable of entering a target cell,

(2) an oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m ,

wherein:

n and m are integers,

AA P2 represents any amino acid,

AA P1 represents any amino acid,

AA P1′ represents any amino acid, and

each AA independently represents an amino acid,

(3) a stabilizing group, and

(4) optionally, a linker group,

wherein the oligopeptide is directly linked to the stabilizing group at a first attachment site of the oligopeptide and the oligopeptide is directly linked to the therapeutic agent or indirectly linked through the linker group to the therapeutic agent at a second attachment site of the oligopeptide, wherein the stabilizing group hinders cleavage of the prodrug by enzymes present in whole blood.

14. The method of claim 13 wherein n is 0 to 3, m is 0 to 3, and m+n is no more than 3 of the oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m .

15. The method of claim 13 wherein AA P1 of the oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m is selected from the group consisting of arginine, alanine, glycine, leucine, methionine, proline, phenylalanine, tyrosine, glutamine, valine, and serine.

16. The method of claim 13 wherein AA P1′ of the oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m is selected from the group consisting of leucine, isoleucine, phenylalanine, valine, tyrosine, and proline.

17. The method of claim 12 wherein the prodrug is administered intravenously to a subject having said tumor.

18. The method of claim 12 wherein the prodrug is resistant to cleavage by TOP.

19. The method of claim 13 wherein AA P1 —AA P1′ of the oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m is selected from the group consisting of Arg-Leu, Arg-Ile, Arg-Phe, Arg-Val, Ala-Phe, Ala-Leu, Gly-Phe, Leu-Phe, Leu-Tyr, Met-Leu, Pro-Phe, Pro-Tyr, Pro-Leu, Phe-Leu, Phe-Phe, Tyr-Ile, Tyr-Pro, Tyr-Leu, Gln-Phe, Val-Tyr, Val-Phe, Gly-Trp, Asp-Phe, and Ser-Leu.

20. The method of claim 13 wherein AA P2 of the oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m is a hydrophobic amino acid.

21. The method of claim 13 wherein AA P2 of the oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m is isoleucine.

22. The method of claim 13 wherein the prodrug is selected from the group consisting of Suc-βAla-Leu-Ala-Leu-Dox SEQ ID NO: 41, Suc-Ile-Ala-Leu-Dox SEQ ID NO: 42, Suc-βAla-Ile-Ala-Leu-Dox SEQ ID NO: 39, Suc-Leu-Ala-Leu-Dox SEQ ID NO: 45, and Suc-Met-Ala-Leu-Dox SEQ ID NO: 73.

23. A method for treating a tumor comprising contacting the tumor with a therapeutically effective amount of a CD10 cleavable prodrug, wherein said tumor is comprised of one or more target cells which express CD10 for at least a portion of the target cell life cycle, wherein the CD10 cleavable prodrug comprises:

(1) a therapeutic agent capable of entering a target cell,

(2) an oligopeptide of the formula (AA) n —AA P2 —AA P1 —AA P1′ —(AA) m ,

wherein:

n and m are integers,

AA P2 represents isoleucine,

AA P1 represents any amino acid,

AA P1′ represents any amino acid, and

each AA independently represents an amino acid,

(3) a stabilizing group, and

(4) optionally, a linker group,

wherein the oligopeptide is directly linked to the stabilizing group at a first attachment site of the oligopeptide and the oligopeptide is directly linked to the therapeutic agent or indirectly linked through the linker group to the therapeutic agent at a second attachment site of the oligopeptide, wherein the stabilizing group hinders cleavage of the prodrug by enzymes present in whole blood.

Assignments (2)
MERGER Recorded Mar 19, 2015
From: MEDAREX, L.L.C.
To: E. R. SQUIBB & SONS, L.L.C.
Reel/Frame 035226/0690 →
MERGER Recorded Jun 13, 2013
From: MEDAREX, INC.
To: MEDAREX, L.L.C.
Reel/Frame 030603/0924 →