US2019255140A1PendingUtilityA1

Uses of hypoxia-inducible factor inhibitors

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Assignee: ONCOIMMUNE INCPriority: Dec 4, 2009Filed: Mar 6, 2019Published: Aug 22, 2019
Est. expiryDec 4, 2029(~3.4 yrs left)· nominal 20-yr term from priority
A61P 35/00A61P 35/02A61K 31/498A61K 38/07A61K 31/00A61K 31/565A61K 45/06A61K 31/4355A61K 38/08A61K 31/395
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Claims

Abstract

The present invention relates to treating, a hematologic cancer using a Hypoxia-Inducible Factor (HIF inhibitor). The invention also relates to inducing acute myeloid leukemia remission using the HIT inhibitor. The invention further relates to inhibiting a maintenance or survival function of a cancer stem cell (CSC) using the HIE inhibitor.

Claims

exact text as granted — not AI-modified
1 . A method for treating a hematologic cancer, comprising administering a Hypoxia-Inducible Factor (HIF) inhibitor to a mammal in need thereof. 
     
     
         2 . The method of  claim 1 , wherein the HIF inhibitor is a HIF1α inhibitor. 
     
     
         3 . The method of  claim 1 , wherein the HIF inhibitor is selected from the group consisting of echinomycin, 2-methoxyestradiol, and geldanamycin. 
     
     
         4 . The method of  claim 1 , wherein the echinomycin is administered at a non-toxic dose. 
     
     
         5 . The method of claim  4 , wherein the dose is 1-100 mcg/m 2 . 
     
     
         6 . The method of claim  3 , wherein the echinomycin is coadministered with a Hedgehog pathway inhibitor. 
     
     
         7 . The method of  claim 6 , wherein the Hedgehog pathway inhibitor is cyclopamine. 
     
     
         8 . The method of  claim 1 , wherein the HIF inhibitor is coadministered with a second cancer therapy. 
     
     
         9 . The method of  claim 1 , wherein the hematological cancer is a leukemia or a lymphoma. 
     
     
         10 . The method of claim  9 , wherein the leukemia is acute myeloid leukemia. 
     
     
         11 . The method of  claim 10 , wherein the mammal carries a cytogenetic alteration. 
     
     
         12 . The method of claim ii, wherein the cytogenetic alteration is selected from the group consisting of:
 47,XY,+21;46,XY;   45,XX,−7;   46,XY,t(8;21)(q22;q22);   49,XX,+8,+8,inv(16)(03.1q22),+21;   46,XX,inv(16)(0.3q22)/46,)0c;   46,XY,inv(16)(03q22);   46,XX,t(2;13)(p23;q 12 )/46,XX;   45,XY,inv(3)(c121q26.2),−7/46,XY;   47,XY,+4,inv(5)(0.5q13)/47,s1,−4,+22;   46,XX,t(11;19)(q23;03.1); 46,XX,t(6;11)(q27;q23)/46,XX; and   46,XX,t(1;17)(03;q25),t(9;11)(p22;q23).   
     
     
         13 . The method of claim  9 , wherein the mammal carries leukemia cells of the phenotype CD 38   31  CD 34 +. 
     
     
         14 . The method of  claim 10 , wherein the mammal carries cancer stem cells. 
     
     
         15 . The method of  claim 14 , wherein the cancer stem cells are multiple drug resistant. 
     
     
         16 . The method of  claim 14 , wherein the cancer stem cells are chemoresistant or radioresistant. 
     
     
         17 . A method for inducing acute myeloid leukemia remission, comprising administering echinomycin to a patient in need thereof. 
     
     
         18 . The method of  claim 17 , wherein the echinomycin is administered at a non-toxic dose. 
     
     
         19 . The method of  claim 18 , wherein the dose is 1-100 mcg/m 2 . 
     
     
         20 . (canceled) 
     
     
         21 . A method for preventing future relapse of acute myeloid leukemia, comprising administering a HIF inhibitor to a patient during remission from acute myeloid leukemia.

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