Ex parte AVNUR et al. - Page 7




                 Appeal No. 95-4473                                                                                                                   
                 Application 08/003,894                                                                                                               


                 examiner's determination that Hill uses an immunogen which reasonably appears to                                                     
                 contain the epitope recognized by a monoclonal antibody produced by hybridoma cell line                                              
                 ATCC No. HB 11106, hybridoma cell line ATCC No. HB 11107, or hybridoma cell line                                                     
                 ATCC No. HB 11108.  On this record, therefore, we find it reasonable to conclude that a                                              
                 person having ordinary skill, armed with the disclosure of Hill, would have produced                                                 
                 monoclonal antibodies which are "functionally equivalent" to the antibodies recited in                                               
                 claims 35 through 37 and which satisfy the criteria set forth in claims 1 through 8, 17                                              
                 through 25, 27 through 29 and 33.                                                                                                    
                          In the briefings before this merits panel, in the Kempe Declaration executed April                                          
                 25, 1994, and in the Kempe Declaration executed September 28, 1994, appellants devote                                                
                 much attention to the claim limitations requiring that their monoclonal antibodies exhibit                                           
                 less than one percent cross-reactivity with liver alkaline phosphatase.  However, we find no                                         
                 error in the examiner's determination that appellants have not                                                                       
                 established that the "cross-reactivity" limitation serves to patentably distinguish over the                                         
                 cited prior art.  On this point, we agree with the findings set forth in the Examiner's                                              


                 Answer and Supplemental Answer.  Note particularly the Supplemental Answer, page 3,                                                  
                 last full paragraph.                                                                                                                 
                          The rejection of claims 1 through 8, 17 through 25, 27 through 29 and 33 on prior art                                       


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