Ex parte CHAROENVIT et al. - Page 10




             Appeal No.  1999-1413                                                                                    
             Application 08/176,024                                                                                   

                    In rejecting claims under 35 U.S.C. § 103, the examiner bears the initial burden of               
             presenting a prima facie case of obviousness.  See In re Rijckaert, 9 F.3d 1531, 1532, 28                
             USPQ2d 1955, 1956 (Fed. Cir. 1993).   A prima facie case of obviousness is established                   
             when the teachings from the prior art itself would appear to have suggested the claimed                  
             subject matter to a person of ordinary skill in the art.  In re Bell, 991 F.2d 781, 783, 26              
             USPQ2d 1529, 1531 (Fed. Cir. 1993).  A reference is considered in its entirety for what it               
             fairly suggests to one skilled in the art.  In re Wesslau, 353 F.2d 238, 241, 147 USPQ 391,              
             393 (CCPA 1965).  With this as background, we analyze the prior art applied by the                       
             examiner in the rejection of the claims on appeal.                                                       
                    According to the examiner, McCutchan 1 and 2 describe monoclonal antibodies                       
             which are specific for epitopes of a peptide which corresponds to a region of the P. Vivax               
             CS (circumsporozite) protein.  The specification, page 2, states that the monoclonal                     
             antibody disclosed by McCutchan et al (Science 230) and McCutchan et al (U.S. Patent                     
             No. 4,693,994) is the monoclonal antibody of the instant invention which is designated                   
             NVS3.  Answer, page 5.  The examiner acknowledges that the McCutchan references do                       
             not teach a composition comprising a pharmaceutical amount of a monoclonal antibody                      
             NVS3 in a pharmaceutically acceptable carrier.   Id.                                                     
                    Harlow is cited by the examiner as establishing that it was well known in the art at              
             the time of the invention to produce solutions of monoclonal antibodies in phosphate                     



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