Ex Parte BUECHLER et al - Page 13



              Appeal No. 2003-2084                                                               Page 13                
              Application No. 08/241,061                                                                                

              antibody or receptor . . . ."  The examiner states that it is "not clear which amount would               
              be sufficient to inhibit binding of the linkage site to the receptor.  The specification no               
              where teaches the amount necessary for the inhibition of binding of the linkage site.                     
              Applicants are requested to include the amount of inhibitors required."  Examiner's                       
              Answer, page 10.                                                                                          
                     The examiner's request for appellants to "include the amount of inhibitors" in the                 
              claims is unreasonable.  As explained in In re Mattison, 509 F.2d 563, 184 USPQ 484                       
              (CCPA 1975), it is proper for a patent applicant to define their invention through use of                 
              functional amounts provided the specification sets forth sufficient guidance so that one                  
              skilled in the art would be able to determine an appropriate amount.  Here, the                           
              examiner has focused on the lack of numerical limitations in the claims and has not                       
              analyzed the specification of this application and explained why there is insufficient                    
              guidance that would allow one to arrive at an appropriate amount.                                         
                     Finally, the examiner rejects claim 102 for reciting "drug of abuse, metabolite of                 
              drug abuse, and analogue of the drug abuse . . . and an analogue of a metabolite of a                     
              therapeutic drug."  The examiner merely states that "the specification does not recite                    
              that the ligand can be either of those.  The specification defines the ligand is a binding                
              partner of a receptor."  As set forth above in regard to the examiner's rejection of claim                
              102 under 35 U.S.C. § 112, first paragraph (written description), we find that the                        
              specification of this application does describe these compounds as being the ligand of                    
              interest in the present invention.                                                                        
                     The examiner's rejection under 35 U.S.C. § 112, second paragraph, is reversed.                     
              5.  Rejection of Claims 98-102 as Anticipated by Kinoshita.                                               




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