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 2Page: Previous 1 2 3 4 5 6 7 8 9 10 11 12 13 NextLast modified: November 3, 2007