Ex Parte ZOLTEWICZ et al - Page 3


                 Appeal No.  2001-1294                                                          Page 3                  
                 Application No.  08/473,667                                                                            
                        “In rejecting claims under 35 U.S.C. § 103, the examiner bears the initial                      
                 burden of presenting a prima facie case of obviousness.  Only if that burden is                        
                 met, does the burden of going forward with evidence or argument shift to the                           
                 applicant.”  In re Rijckaert, 9 F.3d 1531, 1532, 28 USPQ2d 1955, 1956 (Fed. Cir.                       
                 1993).  The test of obviousness is “whether the teachings of the prior art, taken                      
                 as a whole, would have made obvious the claimed invention.”  In re Gorman,                             
                 933 F.2d 982, 986, 18 USPQ2d 1885, 1888 (Fed. Cir. 1991).                                              
                        According to the examiner (Answer, page 4), “Tu disclosed naturally                             
                 occurring nicotine agonists with structural formula as anabaseine and DMBA-                            
                 anabaseine … and their function as a nicotine agonist….”  The examiner also                            
                 finds (Answer, page 7), “Tu taught that anabaseine and DMAB-anabaseine are                             
                 naturally occurring toxin[s] which function as nicotinic agonists and … [are]                          
                 15 times more potent than nicotine….”  The examiner relies on Meyer (Answer,                           
                 page 4) to teach “that anabaseine and DMAB-anabaseine have high affinity in                            
                 animal brain nicotine receptor,” and on Swanson (Answer, page 5) to teach the                          
                 use of “naturally occurring nicotine agonists as therapeutical [sic] agents for                        
                 treating nicotinic receptor pathology i.e. Alzheimer’s disease.”  The examiner                         
                 relies on Remington (Answer, page 4) to teach the preparation of pharmaceutical                        
                 compositions, and on Remington and Rawlins (Answer, page 5) to teach                                   
                 aqueous or liposome formulations.                                                                      
                        The examiner’s statement of the rejection does not address Leeson.  The                         
                 examiner, however, points out (Answer, page 8) that Leeson “described specific                         








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