US2019100758A1PendingUtilityA1

Methods of Treating Colorectal Cancer

Assignee: NOGRA PHARMA LTDPriority: Mar 15, 2013Filed: Jun 7, 2018Published: Apr 4, 2019
Est. expiryMar 15, 2033(~6.6 yrs left)· nominal 20-yr term from priority
C12N 15/1135C12N 2310/315C12N 2310/11A61P 35/00
57
PatentIndex Score
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Claims

Abstract

Disclosed herein are methods for treating/and or preventing colorectal cancer using a specific inhibitor of SMAD7 expression or function. Also disclosed are pharmaceutical compositions containing an inhibitor of SMAD7 for treating and/or preventing colorectal cancer and manufacture of medicaments containing an inhibitor of SMAD7 to be used in treating and/or preventing colorectal cancer.

Claims

exact text as granted — not AI-modified
1 . A method of treating colorectal cancer in a patient suffering from colorectal cancer, the method comprising administering to the patient an effective amount of a SMAD7 antisense oligonucleotide comprising the nucleotide sequence of SEQ ID NO: 10 to the patient. 
     
     
         2 . A method of inhibiting the growth of colorectal cancer cells, comprising inhibiting SMAD7 in the colorectal cancer cells. 
     
     
         3 . A method of treating colorectal cancer or inhibiting the growth of colorectal cancer cells in a patient suffering from colorectal cancer, the method comprising administering to the patient an effective amount of a SMAD7 antisense oligonucleotide comprising the nucleotide sequence of SEQ ID NO: 10. 
     
     
         4 - 7 . (canceled) 
     
     
         8 . The method  claim 1 , wherein the SMAD7 antisense oligonucleotide is administered parenterally. 
     
     
         9 . The method of  claim 1 , wherein the SMAD7 antisense oligonucleotide is administered orally. 
     
     
         10 . The method of  claim 3 , wherein said administering comprises administering a pharmaceutical composition comprising the SMAD7 antisense oligonucleotide and a pharmaceutically acceptable carrier. 
     
     
         11 - 13 . (canceled) 
     
     
         14 . The method of  claim 10 , wherein the pharmaceutical composition is administered parenterally. 
     
     
         15 . The method of  claim 10 , wherein the pharmaceutical composition is administered orally. 
     
     
         16 . The method of  claim 15 , wherein the pharmaceutical composition comprises an enteric coating comprising an ethylacrylate-methacrylic acid copolymer. 
     
     
         17 . The method of  claim 1 , wherein the patient is a human. 
     
     
         18 . The method of  claim 1 , comprising administering at least 100 μg of the SMAD7 antisense oligonucleotide. 
     
     
         19 . The method of  claim 18 , comprising administering from 35 mg to 500 mg of the SMAD7 antisense oligonucleotide. 
     
     
         20 . The method of  claim 3 , wherein the patient is a human. 
     
     
         21 . The method of  claim 3 , comprising administering at least 100 μg of the SMAD7 antisense oligonucleotide. 
     
     
         22 . The method of  claim 21 , comprising administering from 35 mg to 500 mg of the SMAD7 antisense oligonucleotide. 
     
     
         23 . The method of  claim 1 , wherein all of the internucleoside bonds of the nucleotide sequence of SEQ ID NO: 10 are phosphorothioate bonds. 
     
     
         24 . The method of  claim 3 , wherein all of the internucleoside bonds of the nucleotide sequence of SEQ ID NO: 10 are phosphorothioate bonds.

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