Ex Parte DYKSTRA et al - Page 3


                 Appeal No. 2001-1051                                                         Page 3                    
                 Application No.  08/185,079                                                                            

                        According to the rejection:                                                                     
                        This deficiency is cured by the similarity between the respiratory                              
                        syncytial virus (RSV) and the AIDS etiological agent.  RSV and HIV                              
                        are both RNA viruses possessing a similar replicative schema in                                 
                        their respective host cells.  It is noted that Tidwell [ ] reported the                         
                        claimed compounds exhibiting antiviral activity to virus other that                             
                        [sic] the claimed RSV (([Tidwell III]), column 11, lines 43-45).                                
                        Vonderfecht [ ] further motivate[s] the skilled artisan to employ                               
                        these compounds therapeutically on retroviral infection.  Attention                             
                        is directed to page 2015 wherein Vonderfecht [ ] suggest[s] these                               
                        compounds as useful for the claimed retroviral etiological agent.                               
                               Absent information to the contrary, the skilled artisan would                            
                        have been motivated by the data of Tidwell [ ] to employ the                                    
                        claimed compounds against various RNA virus and enjoy a                                         
                        reasonable expectation of success.  Although Tidwell [ ] report[s]                              
                        that the claimed compounds are specific for the RSV etiologial                                  
                        agent, the statement at column 11 and the presented data render                                 
                        such averments moot.                                                                            
                               Thus, two distinct and powerful motivations [exist] [sic] to                             
                        employ Applicants’ compounds in retroviral therapy.  It would follow                            
                        therefore that the instant claims recite prima facie obvious subject                            
                        matter, and are properly rejected under 35 USC 103.                                             
                 Id. at 3-4.                                                                                            
                        Appellants argue that the Tidwell references are all cumulative to one                          
                 another, and all deal with the RSV virus.  According to Appellants, RSV is not a                       
                 retrovirus, but a paramyxovirus and that paramyxovirus and its replicative                             
                 scheme is not analogous to that of a retrovirus.  Vonderfecht, Appellants argue,                       
                 relates to a rotavirus, which again, is not a retrovirus.  Moreover, Appellants                        
                 contend that, contrary to the statement in the rejection that the claimed                              
                 compounds are useful against retroviruses, “Vonderfecht only states that a                             
                 number of viruses require host proteases for productive infection and that                             
                 therefore protease inhibitors MAY have a broad range of antiviral activity.”                           





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