Genetic markers associated with response to crth2 receptor antagonists

Abstract

The present invention provides genetic markers on human chromosome 1 that are associated with a beneficial response to CRTH2 receptor antagonists. These CRTH2 receptor antagonist response markers are useful, inter alia, to identify patients who are most likely to benefit from treatment with CRTH2 receptor antagonist compositions and drug products, in methods of treating patients having a disease susceptible to treatment with a CRTH2 receptor antagonist, and in methods for selecting the most appropriate therapy for such patients.

1 . A method of treating a patient with asthma comprising:
 administering a therapeutically effective amount of {(7R)-4-fluoro-7-[5-(4-fluorobenzyl) -1H-[1,2,3]triazol-1-y1]-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-y1}-acetic acid or a pharmaceutically acceptable salt thereof to the patient,   wherein said patient, prior to the administration of the {(7R)-4-fluoro-7-[5-(4-fluorobenzyl)-1H-[1,2,3]triazol-1-y1]-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-y1}-acetic acid or the pharmaceutically acceptable salt thereof, has tested positive for at least one copy of the G allele of rs12118655   
     
     
         2 . (canceled) 
     
     
         3 . A method of diagnosing in a patient who is susceptible to treatment with {(7R)-4-fluoro-7-[5-(4-fluorobenzyl)-1H-[1,2,3]triazol-1-y1]-6,7,8,9-tetrahydropyrido[1,2-a]indo-10-y1}-acetic acid or a pharmaceutically acceptable salt thereof and treating asthma, said method comprising:
 (a) obtaining a biological sample from a human patient;   (b) detecting whether the G allele of rs12118655 is present in the biological sample;   (c) diagnosing the patient as susceptible to treatment with {(7R)-4-fluoro-7-[5-(4-fluorobenzyl)-1H-[1,2,3]triazol-1-y1]-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-y1}-acetic acid or the pharmaceutically acceptable salt thereof when the presence of the G allele of rs12118655 in the biological sample is detected; and   (d) administering a therapeutically effective amount of {(7R)-4-fluoro-7-[5-(4-fluorobenzyl)-1H-[1,2,3]triazol-1-y1]-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-y1}-acetic acid or the pharmaceutically acceptable salt thereof.   
     
     
         4 . The method of  claim 3 , wherein step (d) further comprises administering a leukotriene receptor antagonist to the patient. 
     
     
         5 . (canceled) 
     
     
         6 . The method of  claim 4 , wherein in step (d) the leukotriene receptor antagonist is montelukast. 
     
     
         7 - 17 . (canceled) 
     
     
         18 . The method of  claim 1 , wherein montelukast is administered to the patient in addition to {(7R)-4-fluoro-7-[5-(4-fluorobenzyl)-1H-[1,2,3]triazol-1-y1]-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-y1}-acetic acid or the pharmaceutically acceptable salt thereof.