Ex parte JANAKY et al. - Page 4




                 Appeal No. 1996-2431                                                                                                                   
                 Application 08/008,186                                                                                                                 
                          II.  Claims 5 through 7, 12 and 14 under 35 U.S.C. § 103 as unpatentable over                                                 
                 Channabasavaiah, Bajusz, Rivier, Sela and Varga.                                                                                       

                          III.  Claims 8 through 10, 12 and 15 under 35 U.S.C. § 103 as unpatentable over                                               
                 Channabasavaiah, Bajusz, Rivier and Stevens.                                                                                           

                          IV.  Claims 16 through 18 under 35 U.S.C. § 103 as unpatentable over                                                          
                 Channabasavaiah, Bajusz, Rivier, Sela, Varga and Stevens.                                                                              

                          Claims 11, 13, 14 and 19 through 23 under 35 U.S.C. § 103 as unpatentable                                                     

                 over Channabasavaiah, Bajusz, Rivier, Stevens, Lin and Anderson.                                                                       


                                                                  DISCUSSION                                                                            
                          The present invention is directed to cytotoxic agonists and antagonists of luteinizing                                        
                 hormone releasing hormone (LHRH).  In each of the claimed LHRH decapeptide analogs,                                                    
                 a cytotoxic agent is conjugated directly or indirectly to the amino acid residue at position                                           
                 six, and the amino acid at position six is always D-Lys or        D-Orn.  We note that both the                                        
                 examiner and appellants have focused throughout the prosecution on those LHRH                                                          
                 agonists and antagonists wherein the cytotoxic moiety is D-melphalan (D-Mel),                                                          
                 anthraquinoyl or methotrexoyl.  As this board functions as a board of review, not a de novo                                            
                 examination tribunal, we shall do likewise. 2                                                                                          




                          235 U.S.C. § 7(b): “The [board] shall . . . review adverse decisions of examiners                                             
                 upon applications for patents . . . “                                                                                                  
                                                                           4                                                                            





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