Ex Parte CLAUSSNER et al - Page 2



            Appeal No. 2001-1221                                                      Page 2             
            Application No. 08/442,957                                                                   
                  According to the examiner (Answer, page 4)                                             
                  Teutsch [teaches] a genus of 19-nor steroid compounds having a keto                    
                  group in the 3-position and double bonds in the 4 and 9 positions and a                
                  substituted phenyl group at the 11-position (cols. 1-6).  The 11-phenyl                
                  group of the compounds are substituted with an alkynyl group of 2 to 8                 
                  carbon atoms which may be substituted with a hydroxy group (col. 1, lines              
                  43-47).  The 17-position substituents include those of the claims (col. 2).            
                  The compounds are taught to have antiprogestomimetic and                               
                  antiglucocorticoid activities.                                                         
            Similarly (id., page 5)                                                                      
                  Loozen teaches a genus of 19-nor steroid compounds having a keto                       
                  group in the 3-position and double bonds in the 4 and 9 positions.  The                
                  compounds have a homocyclic or heterocyclic aryl group in the 11-                      
                  position substituted with a hydrocarbon group of 1-10 carbon atoms which               
                  is substituted with oxo and/or hydroxyl groups (col. 1 to col. 2, line 9).  The        
                  compounds are taught to have antiprogestinic activity (Col. 1, lines 27-29).           
            Further according to the examiner (id., pages 4, 5, and 6), each of the claims               
            differs from the prior art                                                                   
                  by reciting a more limited genus than the reference having an organic                  
                  radical, which may be arylene, attached to the 11-position through a                   
                  carbon atom which terminates in a CH2OH group.  However, it would have                 
                  been obvious to one having ordinary skill in the art at the time of the                
                  invention to select any of the species of the genus taught by the                      
                  reference, including those of the claims having the hydroxy group                      
                  attached to the terminal carbon of the 11-position substituent, because an             
                  ordinary artisan would have the reasonable expectation that any of the                 
                  species of the genus would have similar properties and, thus, the same                 
                  use as the genus as a whole.                                                           
                  There would appear to be no dispute that the claimed species and subgenus are          
            encompassed by the generic 19-nor steroid formulas described in Teutsch and Loozen.          
            Nevertheless, without conceding that the claimed compounds would have been prima             
            facie obvious over the prior art, appellants argue that the references Adescribe final       
            products which have a particular pharmacological activity which is completely non-           
            analogous to Applicants= pharmacological activity,@ thus, Athe decision of [In re            
            Magerlein, 602 F.2d 366, 202 USPQ 473 (CCPA 1979)] is pertinent to the present               




Page:  Previous  1  2  3  4  5  6  Next 

Last modified: November 3, 2007