Ex Parte WOZNEY et al - Page 5




             Appeal No.  1999-1280                                                                              
             Application No.  08/379,813                                                                        

             note that amendments after a final rejection are not a matter of right.  See 37 CFR §              
             1.116 and § 1.195 and MPEP §§ 714.12-714.13, 1207 and 1208.03.  In addition, we                    
             note the non-entry of an amendment is a petitionable, not an appealable, issue.  See               
             37 C.F.R. § 1.181.  Therefore, the “proposed amended claims” are not before this                   
             Merits Panel for review.                                                                           
                   According to the examiner (Answer, pages 6-7):                                               
                                The specification is not enabling for the invention as claimed                  
                          because there is no teaching of other BMP’s.  Supraalveolar                           
                          lesions include melanoma, amalgam tattoo to radiation                                 
                          osteonecrosis and these disorders are not enabled by the                              
                          specification.  Further, the long term augmentation of alveolar                       
                          ridges which are under pressure from dentures is a notably difficult                  
                          achievement and no evidence for the claimed method is shown for                       
                          such a treatment.                                                                     
                   Here, the examiner did not perform the fact-finding needed in order to reach a               
             proper conclusion that the specification does not enable the claimed invention.  The               
             enablement requirement of 35 U.S.C. § 112, first paragraph, requires that the patent               
             specification enable “those skilled in the art to make and use the full scope of the               
             claimed invention without ‘undue experimentation.’”  Genentech, Inc. v. Novo Nordisk               
             A/S, 108 F.3d 1361, 1365, 42 USPQ2d 1001, 1004 (Fed. Cir. 1997)quoting In re                       
             Wright, 999 F.2d 1557, 1561, 27 USPQ2d 1510, 1513 (Fed. Cir. 1993)).                               






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