Triptan Powders for Pulmonary Delivery

Abstract

The invention provides stable, spray-dried, particle formulations containing a triptan, preferably sumatriptan, or a pharmaceutically acceptable salt thereof, which are useful for pulmonary administration to the respiratory tract of a patient for the treatment of disease.

1 . A pharmaceutical composition for pulmonary delivery to the respiratory tract of a patient comprising spray-dried particles of a triptan or a pharmaceutically salt thereof and a pharmaceutically acceptable excipient. 
     
     
         2 . The pharmaceutical composition of  claim 1 , wherein the triptan is sumatriptan or a pharmaceutically acceptable salt thereof. 
     
     
         3 . The pharmaceutical composition of  claim 2 , wherein the triptan is sumatriptan succinate. 
     
     
         4 . The pharmaceutical composition of  claim 1 , wherein the triptan is sumatriptan free base. 
     
     
         5 . The pharmaceutical composition of  claim 1 , wherein the pharmaceutical excipient comprises one or more of: a phospholipid, a salt, an amino acid or a sugar. 
     
     
         6 - 8 . (canceled) 
     
     
         9 . The pharmaceutical composition of  claim 1 , wherein the particles comprise sumatriptan or a pharmaceutically acceptable salt thereof, DPPC, sodium chloride and maltodextrin. 
     
     
         10 . The pharmaceutical composition of  claim 1 , wherein the particles comprise sumatriptan or a pharmaceutically acceptable salt thereof, DPPC, sodium chloride and l-leucine. 
     
     
         11 . The pharmaceutical composition of  claim 1 , wherein the particles comprise 5 to 50% triptan or a pharmaceutically acceptable salt thereof, 5-20% phospholipid, and 1-10% sodium chloride as measured by percent of dry solids in the powder. 
     
     
         12 . The pharmaceutical composition of  claim 1 , wherein the particles comprise 25 to 55% triptan or a pharmaceutically acceptable salt thereof, 5-20% phospholipid, 1-10% sodium chloride and 25 to 60% of an excipient selected from maltodextrins, lactose, glycine, trehalose, mannitol and 1-leucine, as measured by percent of dry solids in the powder. 
     
     
         13 . The pharmaceutical composition of  claim 11 , wherein the triptan is sumatriptan free base or a sumatriptan salt. 
     
     
         14 . The pharmaceutical composition of  claim 13 , wherein the particles comprise 25 to 55% sumatriptan free base, 15-20% phospholipid, 1-5% sodium chloride and 25 to 55% of an excipient selected from maltodextrins, and 1-leucine, as measured by percent of dry solids in the powder. 
     
     
         15 . The pharmaceutical composition of  claim 14 , wherein the particles comprise 30 to 50% sumatriptan free base, about 18% phospholipid, about 2% sodium chloride and 30 to 50% of an excipient selected from maltodextrins or 1-leucine as measured by percent of dry solids in the powder. 
     
     
         16 . The pharmaceutical composition of  claim 15 , wherein the phospholipid is DPPC. 
     
     
         17 . The pharmaceutical composition of  claim 15  wherein the maltodextrin is (i) maltodextrin with D.E.=10.7 or (ii) SD-30. 
     
     
         18 . The pharmaceutical composition of  claim 15  comprising 1-leucine. 
     
     
         19 . A powder formulation for pulmonary delivery to the respiratory tract of a patient, said powder comprising particles having a composition selected from the table below, as measured by weight percent of dry solids in the powder: 
       
         
           
                 
                 
                 
                 
                 
               
                     
                 
                   Sumatriptan 
                     
                   Sodium 
                     
                     
                 
                   Succinate 
                   DPPC 
                   Chloride 
                   l-leucine 
                   Sugar/Sugar alcohol 
                 
                     
                 
                   25% 
                   18% 
                   2% 
                   55% 
                   0 
                 
                   50% 
                   18% 
                   2% 
                   30% 
                   0 
                 
                   50% 
                   18% 
                   2% 
                   0 
                   30% maltodextrin 
                 
                   50% 
                   18% 
                   2% 
                   0 
                   30% lactose 
                 
                   50% 
                   18% 
                   2% 
                   0 
                   30% mannitol 
                 
                   50% 
                   18% 
                   2% 
                   0 
                   30% trehalose 
                 
                   25% 
                   18% 
                   2% 
                   0 
                   55% trehalose 
                 
                     
                 
             
                
                
                
                
               
               
                
                
                
                
                
                
                
                
               
            
           
         
       
     
     
         20 . A powder formulation for pulmonary delivery to the respiratory tract of a patient, said powder comprising particles having a composition selected from the table below, as measured by weight percent of dry solids in the powder: 
       
         
           
                 
                 
                 
                 
                 
               
                     
                 
                   Sumatriptan 
                     
                   Sodium 
                     
                     
                 
                   Free base 
                   DPPC 
                   Chloride 
                   Amino Acid 
                   Sugar/Sugar alcohol 
                 
                     
                 
                   50% 
                   18% 
                   2% 
                   30% leucine 
                   0 
                 
                   50% 
                   18% 
                   2% 
                   0 
                   30% maltodextrin 
                 
                   50% 
                   18% 
                   2% 
                   0 
                   30% lactose 
                 
                   50% 
                   18% 
                   2% 
                   30% glycine 
                   0 
                 
                     
                 
             
                
                
                
                
               
               
                
                
                
                
                
               
            
           
         
       
     
     
         21 . (canceled) 
     
     
         22 . A method of treating migraine in a subject in need thereof, comprising administering to the pulmonary system of the subject a therapeutically effective amount of the pharmaceutical composition of  claim 1 . 
     
     
         23 . A method of treating cluster headache in a subject in need thereof, comprising administering to the pulmonary system of the subject a therapeutically effective amount of the powder formulation of  claim 1 .