Ex Parte Kovesdi et al - Page 8




                 Appeal No. 2004-1259                                                                                                             
                 Application No. 09/832,355                                                                                                       
                 contemplated.   While, the specification also provides for preferred truncated forms of                                          
                 HBNF peptide having various percentage amounts of the HBNF peptide, the                                                          
                 specification does not exclude the full length peptide and thus would appear to                                                  
                 reasonably support a claim to “at least about 60% of the wild-type HBNF or MK amino                                              
                 acid sequence.”                                                                                                                  
                         The rejection of claim 31 for lack of written description is reversed.                                                   


                 Enablement and Written Description                                                                                               
                         Claims 1-7, 9, 12, 16-19, 30-41 and 43-46 stand rejected under 35 U.S.C.                                                 
                 §112, first paragraph for lack of enablement and lack of adequate written description.                                           
                         The examiner raises several issues of lack of written description and enablement                                         
                 with respect to the claims.  We address them, in turn, below.                                                                    


                 1.   Lack of Enablement VEGF Protein                                                                                             
                         The examiner argues that the claims in the application “are extremely broad,                                             
                 encompassing a fusion protein of any possible VEGF protein that does not bind to                                                 
                 heparin, to any other cytokine with any angiogenic or bone growth activity.  Overall, the                                        
                 specification does not teach how to make and use the invention in a manner                                                       
                 commensurate in scope with the claims, and does not provide an adequate written                                                  
                 description to support the claimed scope.”  Answer, pages 7-8.                                                                   



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