Ex parte ORLOWSKI et al. - Page 5




             Appeal No. 1995-4370                                                                                    
             Application 07/401,432                                                                                  


                    According to the examiner, Brugger, Riniker, Orlowski I, Sakakibara, Orlowski II,                
             Rittel I and Rittel II disclose calcitonin analogs which differ from the claimed analogs in that        
             the claimed analogs have “an amide bridge at positions one and six of the peptide                       
             sequence as opposed to the disulfide bridge of each of the above-cited prior art,” while                
             “Fujii discloses that a peptide sequence having an amide linkage has a considerably                     
             improved stability as compared to the unstable disulfide bridge.”  See page 5 of the                    
             Answer.                                                                                                 
                    The examiner concludes that “it would have been obvious to one having ordinary                   
             skill in the art at the time the invention was made to replace the disulfide bridge in anyone           
             of the peptide sequences of e.g., Brugger with an amide linkage for the advantages taught               
             by Fujii.”  See page 5 of the Answer.                                                                   
                    In our judgment, the combined disclosures of the references are insufficient to reach            
             the subject matter on appeal.  None of the references discloses an analog with the amino                
             acid sequence required by the claims.  The statement of the rejection does not                          
             acknowledge this fact, much less provide reasons why one skilled in the art would have                  
             found it obvious to modify the amino acid sequences of the prior art analogs to                         
             arrive at the present analogs.  Further, Fujii discloses a number of calcitonin analogs with            
             amide bridges, but there is nothing in the reference, or in the examiner’s reasoning, which             




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