US2015238575A1PendingUtilityA1

Methods and compositions for the treatment of cancer

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Assignee: QUINTESSENCE BIOSCIENCES INCPriority: Jul 17, 2006Filed: Apr 27, 2015Published: Aug 27, 2015
Est. expiryJul 17, 2026(~0 yrs left)· nominal 20-yr term from priority
C12Y 301/27005A61P 35/00A61P 31/14A61K 38/465A61K 47/10A61K 38/00A61P 35/04A61K 45/06A61N 5/10C12N 9/22
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Claims

Abstract

The present invention is directed toward the delivery of toxic agents to pathogenic cells, particularly cancer cells. In some embodiments, the toxic agent is a human ribonuclease or similar agent that is toxic to cells.

Claims

exact text as granted — not AI-modified
We claim: 
     
         1 . A method of treating a subject comprising: administering a human ribonuclease comprising polyethylene glycol to the subject. 
     
     
         2 . The method of  claim 1 , wherein the ribonuclease is a wild type human ribonuclease (human RNase). 
     
     
         3 . The method of  claim 1 , wherein said subject is a research subject. 
     
     
         4 . The method of  claim 1 , wherein said subject has a disease. 
     
     
         5 . The method of  claim 4 , wherein said disease is a disease characterized by aberrant cell growth. 
     
     
         6 . The method of  claim 5 , wherein said disease is cancer. 
     
     
         7 . The method of  claim 4 , wherein said disease is a vascular disease. 
     
     
         8 . The method of  claim 4 , wherein said disease is an inflammatory disease. 
     
     
         9 . The method of  claim 4 , wherein said disease is an autoimmune disease. 
     
     
         10 . The method of  claim 1 , wherein said subject has an infection. 
     
     
         11 . The method of  claim 1 , wherein said subject has a degenerative condition. 
     
     
         12 . The method of  claim 1 , wherein the ribonuclease is administered at 0.01 to 100 mg/kg body weight of the subject per week for one or more weeks. 
     
     
         13 . The method of  claim 1 , wherein the ribonuclease is administered at 0.01 to 100 mg/kg body weight of the subject per day for one or more days. 
     
     
         14 . The method of  claim 1 , wherein the ribonuclease is administered at 0.01 to 100 mg/kg body weight of the subject per treatment for one or more treatments. 
     
     
         15 . The method of  claim 1 , wherein the ribonuclease is co-administered with one or more other medical interventions. 
     
     
         16 . The method of  claim 15 , wherein the co-administration is simultaneous. 
     
     
         17 . The method of  claim 15 , wherein the co-administration is sequential.

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