US2018153828A1PendingUtilityA1

Methods for treating cancer

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Assignee: RADIUS PHARMACEUTICALS INCPriority: Apr 29, 2015Filed: Oct 26, 2017Published: Jun 7, 2018
Est. expiryApr 29, 2035(~8.8 yrs left)· nominal 20-yr term from priority
A61K 31/675A61K 45/06A61K 31/137A61P 35/00A61P 35/04A61K 31/436A61K 31/519A61K 2300/00A61K 31/506A61K 31/138A61K 31/565A61K 31/5685A61K 31/685
65
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Claims

Abstract

Disclosed herein are methods of inhibiting tumor growth or producing tumor regression in a subject having a drug-resistant estrogen receptor alpha positive cancer or a mutant estrogen receptor alpha positive cancer. The methods entail administering to the subject a therapeutically effective amount of RAD1901 having the structure: or a salt or solvate thereof.

Claims

exact text as granted — not AI-modified
1 . A method of inhibiting tumor growth or producing tumor regression in a subject having a estrogen receptor alpha-positive cancer that has a mutant estrogen receptor alpha comprising administering to said subject a therapeutically effective amount of RAD1901 having the structure: 
       
         
           
           
               
               
           
         
         or a salt or solvate thereof. 
       
     
     
         2 . (canceled) 
     
     
         3 . The method of  claim 1 , wherein the cancer is breast cancer. 
     
     
         4 . The method of  claim 3 , wherein the cancer is a metastatic breast cancer. 
     
     
         5 . The method of  claim 3 , wherein said cancer is positive for the mutant estrogen receptor alpha comprising one or more mutations selected from the group consisting of Y537X1, L536X2, P535H, V534E, S463P, V392I, E380Q and combinations thereof, wherein:
 X1 is S, N, or C, D538G; and X2 is R or Q.   
     
     
         6 . The method of  claim 5 , wherein the mutation is Y537S. 
     
     
         7 . The method of  claim 3  wherein the ratio of the concentration of RAD1901 or a salt or solvate thereof in the tumor to the concentration of RAD1901 or a salt or solvate thereof in plasma (T/P) following administration is at least about 15. 
     
     
         8 . The method of  claim 3  wherein said subject has osteoporosis or a high risk of osteoporosis. 
     
     
         9 . The method of  claim 3  wherein the subject is a pre-menopausal woman. 
     
     
         10 . The method of  claim 3  wherein the subject is a post-menopausal woman who had relapsed or progressed after previous treatment with SERMs and/or AIs. 
     
     
         11 . The method of  claim 3  wherein the therapeutically effective amount is about 150 to about 1,500 mg q.d. 
     
     
         12 . The method of  claim 3 , wherein the salt thereof is RAD1901 dihydrochloride. 
     
     
         13 . The method of  claim 4 , wherein the tumor is resistant to a drug selected from the group consisting of anti-estrogens, aromatase inhibitors, and combinations thereof. 
     
     
         14 . The method of  claim 13 , wherein the anti-estrogen is tamoxifen or fulvestrant. 
     
     
         15 . The method of  claim 13 , wherein the aromatase inhibitor is anastrozole, letrozole or aromasin. 
     
     
         16 . The method of  claim 3  wherein the therapeutically effective amount is 150 mg to 2,000 mg. 
     
     
         17 . The method of  claim 3 , wherein the therapeutically effective amount is 200 mg, 400 mg, or 500 mg.

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