Ex parte TSAY et al. - Page 5




              Appeal No. 95-1231                                                                                              
              Application No. 07/689,215                                                                                      


              claim language.  We find ourselves in agreement with appellants' statement at page 4 of                         
              the Appeal Brief (Brief) which states:                                                                          
                             In reading the claims, one skilled in the art would understand that after                        
                      the contact of the test product with the human serum, C1r may be reduced                                
                      and C4a may be generated within the serum.  Hence, the serum then                                       
                      becomes the reagent used in the separate measurements of step (B).                                      

              We read the term "the" which precedes the phrase "human serum" in line 2 of step (A) to                         
              be indicative of an antecedent basis for the subject serum.  We find no reference to the                        
              control human serum in the claim prior to this usage. The only use of the phrase "human                         
              serum" which precedes the use of the phrase in line 2 of Step (A) is that serum which has                       
              been contacted with the immunoglobulin product being tested.  We conclude that the                              
              phrase "the human serum" refers to that serum previously contacted with the                                     
              immunoglobulin product.  We note that to accept the examiner's interpretation of the                            
              phrase as being directed not to the previously contacted human serum, but instead to                            
              human serum intended to act as the control, renders the claimed method of determining                           
              the anticomplement activity of the immunoglobulin product meaningless. Such a reading                           
              would result in data relating to the control serum and would not produce a determination of                     
              the anticomplement activity of the immunoglobulin product.  We                                                  


              choose not to give the claims such an unreasonable interpretation which is inconsistent                         
              with the invention as described in the specification.                                                           

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