US2008221068A1PendingUtilityA1

Anti-tumor agents

Assignee: POINT THERAPEUTICS INCPriority: May 25, 1999Filed: Oct 15, 2007Published: Sep 11, 2008
Est. expiryMay 25, 2019(expired)· nominal 20-yr term from priority
A61P 35/00A61K 31/69A61K 38/00A61K 45/06
63
PatentIndex Score
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Claims

Abstract

A method for treating subjects with abnormal cell proliferation is provided. The method involves administering to subjects in need of such treatment an effective amount of an agent of Formula I, to inhibit cell proliferation such as that associated with tumor growth and metastasis. A method for inhibiting angiogenesis in an abnormal proliferative cell mass by the administration of an agent of Formula I is also provided.

Claims

exact text as granted — not AI-modified
1 . A method for treating a subject having a condition characterized by an abnormal mammalian cell proliferation, comprising:
 administering to a subject in need of such treatment, an agent in an amount effective to inhibit the proliferation, wherein the agent is a compound of Formula I.   
     
     
         2 . The method of  claim 1 , wherein the abnormal mammalian cell proliferation is manifested as a tumor. 
     
     
         3 . The method of  claim 1 , wherein the condition is further characterized by the presence of reactive stromal fibroblasts. 
     
     
         4 . The method of  claim 1 , wherein the abnormal mammalian cell proliferation is in epithelial cells. 
     
     
         5 . The method of  claim 4 , wherein the abnormal mammalian cell proliferation is selected from the group consisting of a carcinoma, a sarcoma, and a melanoma. 
     
     
         6 . The method of  claim 1 , wherein the condition is a metastasis of epithelial origin. 
     
     
         7 . The method of  claim 1 , wherein the condition is selected from the group consisting of breast cancer, colorectal cancer, ovarian cancer prostate cancer, pancreatic cancer, kidney cancer, lung cancer, melanoma and fibrosarcoma. 
     
     
         8 . The method of  claim 1 , wherein the condition is selected from the group consisting of bone and connective tissue sarcomas. 
     
     
         9 . The method of  claim 1 , wherein the agent is administered locally. 
     
     
         10 . The method of  claim 1 , wherein the agent is administered systemically. 
     
     
         11 . The method of  claim 1 , wherein the subject is otherwise free of symptoms calling for hemopoietic stimulation. 
     
     
         12 . The method of  claim 1 , wherein the agent is administered in combination with surgery to remove an abnormal proliferative cell mass. 
     
     
         13 . The method of  claim 1 , wherein the agent is administered to a patient who has had surgery to remove an abnormal proliferative cell mass. 
     
     
         14 . The method of  claim 1 , wherein the agent is administered in combination with an anti-cancer compound. 
     
     
         15 . The method of  claim 1 , wherein the agent is targeted to a tumor. 
     
     
         16 . The method of  claim 1 , wherein the subject has normal hemopoietic activity. 
     
     
         17 . The method of  claim 1 , wherein the subject is HIV negative. 
     
     
         18 . The method of  claim 1 , wherein the agent is Val-boro-Pro. 
     
     
         19 . A method for inhibiting angiogenesis in a subject having a condition characterized by abnormal mammalian cell proliferation comprising:
 administering to a subject in need of such treatment, an agent in an amount effective to inhibit angiogenesis in an abnormal proliferative cell mass, wherein the agent is a compound of Formula I.   
     
     
         20 . The method of  claim 19 , wherein the abnormal mammalian cell proliferation is manifested as a tumor. 
     
     
         21 . The method of  claim 19 , wherein the abnormal mammalian cell proliferation is in epithelial cells. 
     
     
         22 . The method of  claim 19 , wherein the abnormal mammalian cell proliferation is selected from the group consisting of a carcinoma, a sarcoma, and a melanoma. 
     
     
         23 . The method of  claim 19 , wherein the condition is a metastasis. 
     
     
         24 . The method of  claim 19 , wherein the condition is selected from the group consisting of breast cancer, colorectal cancer, ovarian cancer, prostate cancer, pancreatic cancer, kidney cancer, lung cancer, melanoma and fibrosarcoma. 
     
     
         25 . The method of  claim 19 , wherein the agent is administered locally. 
     
     
         26 . The method of  claim 19 , wherein the agent is administered systemically. 
     
     
         27 . The method of  claim 19 , wherein the subject is free of symptoms calling for hemopoietic stimulation. 
     
     
         28 . The method of  claim 19 , wherein the agent is administered in combination with surgery to remove an abnormal proliferative cell mass. 
     
     
         29 . The method of  claim 19 , wherein the agent is administered to a patient who has had surgery to remove an abnormal proliferative cell mass. 
     
     
         30 . The method of  claim 19 , wherein the agent is administered in combination with an anti-cancer compound. 
     
     
         31 . The method of  claim 19 , wherein the agent is administered in combination with an anti-angiogenic compound. 
     
     
         32 . The method of  claim 19 , wherein the subject has normal hemopoietic activity. 
     
     
         33 . The method of  claim 19 , wherein the subject is HIV negative. 
     
     
         34 . The method of  claim 19 , wherein the agent is Val-boro-Pro. 
     
     
         35 . The method of  claim 19 , wherein the agent is targeted to a tumor. 
     
     
         36 . A pharmaceutical preparation comprising:
 an agent of Formula I,   at least one other anti-cancer compound, and   a pharmaceutically acceptable carrier.   
     
     
         37 . A pharmaceutical preparation comprising:
 an agent of Formula I,   at least one other anti-angiogenic compound, and   a pharmaceutically acceptable carrier.

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