Ex Parte Latta - Page 9

                Appeal 2007-1152                                                                             
                Application 10/660,924                                                                       
                      The Examiner has provided no other explanation as to why the claim                     
                is not adequately enabled for the claimed method of preventing onset of                      
                Type I diabetes.  Thus, on the record before us, we conclude that the                        
                Examiner has not sustained the burden of establishing a reasonable basis to                  
                question the scope of enablement of the claimed invention. We reverse the                    
                rejection of claims 2-9 for lack of enablement                                               

                Written description rejection                                                                
                      Under 35 U.S.C. § 112, first paragraph, the specification must contain                 
                a written description of the invention.  Thus, when claims are amended                       
                during patent prosecution, the claimed invention, in its amended form, must                  
                be described in the specification.  “An applicant complies with the written                  
                description requirement ‘by describing the invention, with all its claimed                   
                limitations.’  Lockwood v. American Airlines, Inc., 107 F.3d 1565, 1572, 41                  
                USPQ2d 1961, 1966 (1997).” Gentry Gallery v. The Berkline Corp., 134                         
                F.3d 1473, 1479, 45 USPQ2d 1498, 1502-1503 (Fed. Cir. 1998).                                 
                      The Examiner contends that claims 2-9, which were added by an                          
                amendment dated April 1, 2004, are not described in the Specification as it                  
                was originally filed (Answer 8).  The Examiner argues that the Specification                 
                “as originally filed only disclosed [a] two-step process” involving tolerizing               
                and curative doses (Answer 12), not a one-step method of “preventing type I                  
                diabetes comprising … implanting a tolerizing dose of insulin-secreting                      
                cells” in which the dose is at least one order of magnitude less than a                      
                curative dose (Answer 12).  We do not agree.                                                 




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