Ex Parte HOSOKAWA et al - Page 2




              Appeal No. 2002-1358                                                                                         
              Application No. 09/467,903                                                                                   
                     30.  A pharmaceutical composition comprising a therapeutically effective amount                       
              of a monoclonal antibody fragment bound to the surface of a liposome enclosing an                            
              anti-cancer agent or toxin to cancer cells and a pharmaceutically acceptable carrier                         
              therefor,                                                                                                    
                     said liposome comprising phosphatidylcholine, cholesterol and                                         
              phosphatidylethanolamine,                                                                                    
                     said liposome being modified with poly(ethylene glycol), wherein the                                  
              poly(ethylene glycol) is bound to the surface of the liposome through a maleimide                            
              group,                                                                                                       
                     said antibody fragment belonging to IgG class or IgM class and specifically                           
              binding to a surface antigen of a stomach and colon cancer cell membrane, and                                
                     said antibody fragment having a variable region of the heavy chain which                              
              comprises the amino acid sequence shown in SEQ ID No: 5 and having a variable                                
              region of the light chain which comprises the amino acid sequence of SEQ ID No:6.                            
                     34.  The pharmaceutical composition of claim 30, wherein the monoclonal                               
              antibody fragment is a F(ab')2 antibody fragment.                                                            

                     No prior art references are relied upon by the examiner.                                              
                     The references relied upon by the appellants are:                                                     
              Wright et al (Wright, “Antibody-directed liposomes as drug delivery vehicles,” Advanced                      
              Drug Delivery Reviews, Vol. 3, pp. 343-389 (1989)                                                            
              Singhal et al (Singhal), “Antibody-mediated targeting of liposomes to erythrocytes in                        
              whole blood,” Biochimica et Biophysica Acta, Vol. 880, pp. 72-77 (1996)                                      
              Traut et al. (Traut), “Methyl 4- Mercaptobutyrimidate as a Cleavable Cross-Linking                           
              Reagent and Its Application to the Escherichia coli 30S Ribosome,” Biochemistry, Vol.                        
              12, No. 17 (1973)                                                                                            

              Procedural Background                                                                                        
                     The original claims in the application were directed to a human monoclonal                            
              antibody and an anti-cancer formulation comprising the antibody.   Appellants filed a                        
              preliminary amendment (Paper No. 2, Dec. 21, 1999), amending the claims to recite a                          

                                                            2                                                              





Page:  Previous  1  2  3  4  5  6  7  8  9  10  11  12  13  Next 

Last modified: November 3, 2007