IP Library Granted Patent US 9,682,090
Granted Patent B2
US 9,682,090 · App. 14/941,281 · Granted Jun 20, 2017

Methods for treating and preventing prostate cancer bone metastases

Inventor: Colm Morrissey (Seattle, WA)
Assignee: University of Washington
A61K31/662A61K31/00
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Quick Facts
Patent No.
US 9,682,090
App. No.
14/941,281
Granted
Jun 20, 2017
Kind
B2
Abstract

Methods for treating a subject having a prostate cancer bone metastasis are disclosed. Methods for prophylactically treating a subject at risk of developing a prostate cancer bone metastasis are also disclosed. The methods for treating a subject having, or at risk of developing, a prostate cancer bone metastasis may include administering a prostatic acid phosphatase inhibiting agent to the subject. The methods for treating a subject having, or at risk of developing, a prostate cancer bone metastasis may also include administering a phosphonic acid to the subject. Further, the phosphonic acid may include a benzylaminophosphonic acid, such as [phenyl[(phenylmethyl)amino]methyl]-phosphonic acid).

Claims (22)

1. A method for treating a subject having an osteoblastic prostate cancer bone metastasis, comprising:

administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising a benzylaminophosphonic acid, a biologically active derivative of a benzylaminophosphonic acid, or a pharmaceutically acceptable salt, ester, solvate, isomer, or complex thereof.

2. The method of claim 1 , wherein the benzylaminophosphonic acid is [phenyl[(phenylmethyl)amino]methyl]-phosphonic acid.

3. The method of claim 1 , wherein the pharmaceutical composition is an inhibitor of prostatic acid phosphatase (PAP).

4. The method of claim 1 , wherein the pharmaceutical composition reduces a pathological effect or symptom of the prostate cancer bone metastasis.

5. The method of claim 4 , wherein the pathological effect or symptom of the osteoblastic prostate cancer bone metastasis is selected from at least one of bone pain, a bone fracture, spinal cord compression, and an increased blood calcium level.

6. The method of claim 1 , wherein the subject has at least one of stage III prostate cancer, stage IV prostate cancer, and castration-resistant prostate cancer.

7. The method of claim 1 , further comprising:

identifying the subject having the osteoblastic prostate cancer bone metastasis.

8. The method of claim 1 , wherein the subject is a human or a mammal.

9. A method for prophylactically treating a subject at risk of developing an osteoblastic prostate cancer bone metastasis, comprising:

administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising a benzylaminophosphonic acid, a biologically active derivative of a benzylaminophosphonic acid, or a pharmaceutically acceptable salt, ester, solvate, isomer, or complex thereof.

10. The method of claim 9 , wherein the benzylaminophosphonic acid is [phenyl[(phenylmethyl)amino]methyl]-phosphonic acid.

11. The method of claim 9 , wherein the pharmaceutical composition is an inhibitor of prostatic acid phosphatase (PAP).

12. The method of claim 9 , wherein the pharmaceutical composition reduces the risk of developing the prostate cancer bone metastasis.

13. The method of claim 9 , further comprising:

identifying a subject having prostate cancer or at risk of developing an osteoblastic prostate cancer bone metastasis.

14. The method of claim 9 , wherein the subject has at least one of stage III prostate cancer, stage IV prostate cancer, and castration-resistant prostate cancer.

15. The method of claim 9 , wherein the subject is a human or a mammal.

16. A method for treating a pathological effect or symptom of an osteoblastic prostate cancer bone metastasis in a subject, comprising:

administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising a prostatic acid phosphatase (PAP) inhibiting agent, wherein the PAP inhibiting agent is selected from the group consisting of a benzylaminophosphonic acid, a biologically active derivative of a benzylaminophosphonic acid, and a pharmaceutically acceptable salt, ester, solvate, isomer, and complex thereof.

17. The method of claim 16 , wherein the PAP inhibiting agent is [phenyl[(phenylmethyl)amino]methyl]-phosphonic acid.

Assignments (2)
CONFIRMATORY LICENSE Recorded Nov 22, 2016
From: UNIVERSITY OF WASHINGTON
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 040668/0263 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 17, 2015
From: MORRISSEY, COLM
To: UNIVERSITY OF WASHINGTON
Reel/Frame 037321/0522 →
Continuity (2)
Provisional Application 62079698 · Nov 14, 2014
Related Publication 20160136189A1 · May 19, 2016