Ex Parte HIRSCHMAN - Page 3


                 Appeal No. 2004-1212                                                           Page 3                    
                 Application No. 09/316,624                                                                               

                                                       Discussion                                                         
                         Claim 1, the broadest claim on appeal, is directed to a method for                               
                 ameliorating a symptom of rheumatoid arthritis comprising parenterally                                   
                 administering “an effective symptom ameliorating amount of Product R in a range                          
                 from about 2.5 microliters to about 40 microliters per kilogram of body weight per                       
                 day.”  The examiner rejected the claims as indefinite and anticipated.                                   
                 1.  Definiteness                                                                                         
                         The examiner rejected the claims under 35 U.S.C. § 112, second                                   
                 paragraph, on the basis that “[t]he metes and bounds of the phrase ‘effective                            
                 symptom ameliorating amount’ in claims 1 and 4 are unclear.”  Examiner’s                                 
                 Answer, page 3.                                                                                          
                         Appellant argues that “[t]here is nothing unclear about the claim language                       
                 ‘an effective symptom ameliorating amount of Product R in a range from about                             
                 2.5 microliters to about 40 microliters per kilogram of body weight per day’[;] . . .                    
                 Product R is a substance in liquid form made according to a specific process                             
                 described in the application.”  Appeal Brief, page 9.                                                    
                         We agree with Appellant that the claims mean what they say:  an                                  
                 “effective symptom ameliorating amount” of Product R is a daily dosage of 2.5 to                         
                 40 µl per kilogram of the patient’s body weight.  The specification defines Product                      
                 R as the product resulting from one of two described procedures, and the claims                          
                 require administration of defined quantities of that (liquid) product.  The claim                        
                 language that the examiner objected to – “effective symptom ameliorating                                 
                 amount” – is essentially duplicative of the quantities expressly recited in the                          





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