Ex Parte MCDONNELL et al - Page 6


              Appeal No. 2003-2091                                                               Page 6                
              Application No. 09/266,465                                                                               

                     one must select particular species of gene from a very large genus, and                           
                     then select a particular species of promoter form a similarly large genus of                      
                     possible promoters.  And even then, the claimed invention is still not                            
                     taught, as these particular elements must be combined.  Forcing the                               
                     skilled artisan to make each of these selection[s] is akin to asking . . . that                   
                     person to modify the prior art.  That is not anticipation.                                        
              Id., page 9.                                                                                             
                     We agree with Appellants that Zhang does not anticipate the instant claims.                       
              “Under 35 U.S.C. § 102, every limitation of a claim must identically appear in a single                  
              prior art reference for it to anticipate the claim.”  Gechter v. Davidson, 116 F.3d 1454,                
              1457, 43 USPQ2d 1030, 1032 (Fed. Cir. 1997).  “Every element of the claimed                              
              invention must be literally present, arranged as in the claim.”  Richardson v. Suzuki                    
              Motor Co., Ltd., 868 F.2d 1226, 1236, 9 USPQ2d 1913, 1920 (Fed. Cir. 1989).                              
                     The examiner has not pointed to a single, specific construct disclosed by Zhang                   
              that includes all of the limitations of the instant claims.  Rather, the examiner has                    
              pointed to the disclosure in Zhang’s columns 2, 25, 27-30, and 38-39.  Those columns                     
              describe particular promoters that can be used in adenoviral vectors (column 2, lines                    
              34-38, and columns 27-30), specific therapeutic genes that can be included in                            
              adenoviral vectors as cancer treatment agents (column 2, lines 46-57, and columns 23-                    
              26), and pharmaceutical compositions (columns 38-39).  Thus, as Appellants point out,                    
              deriving the claimed adenoviral constructs from Zhang’s disclosure requires picking a                    
              promoter from among the many promoters disclosed by Zhang, some of which are not                         
              inducible and some of which are not non-adenoviral promoters, then picking a                             
              therapeutic gene from among the many possible genes disclosed by Zhang, only a few                       
              of which are proapoptotic members of the Bcl-2 gene family.                                              






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