Ex parte KOSLEY JR. et al. - Page 6




          Appeal No. 1997-2182                                                        
          Application 08/137,443                                                      
          depicted by formula (II) in claim 1 and also includes the                   
          "pharmaceutically acceptable addition salts" thereof.  The                  
          terminology "pharmaceutically acceptable addition salts" is                 
          conventional language used to describe well-known groups of                 
          compounds (salts) prepared from various acids and the claimed               
          compounds.  The salts are usually prepared for purposes of                  
          solubility and bioavailability.  See appellants' disclosure at              
          page 7, lines 22 through 25 for acids useful for preparing the              
          claimed salts.                                                              
               Appellants' composition claim is a so-called "comprising"              
          claim and, as such, is directed to compositions including the               
          recited carrier and an acetylcholinesterase inhibiting amount               
          of the compounds defined by claim 1.  The compositions are                  
          open to the inclusion of compounds such as those described by               
          appellants in their specification at page 7, line 26 through                
          page 9, line 10.  The compositions do not exclude any other                 
          materials, including materials disclosed but not claimed and                
          materials neither disclosed nor even contemplated.                          
               Appellants' method claim is directed to treating memory                
          dysfunction characterized by decreased cholinergic function by              
          administering the compounds of claim 1 to a mammal in an                    
          amount effective to inhibit AchE.  Thus, the claimed method is              
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