Ex parte WOODLE et al. - Page 2




          Appeal No. 95-4004                                                          
          Application 07/858,171                                                      
          GRON, Administrative Patent Judge.                                          
                      DECISION ON APPEAL UNDER 35 U.S.C. § 134                        
               This is an appeal from an examiner’s rejection of Claims 1             
          and 4-7, all claims pending in this application.  Claims 1 and              
          4-7 stand finally rejected under 35 U.S.C. § 103 as unpatentable            
          over the teaching of Popescu et al. (Popescu), U.S. 4,981,692,              
          patented January 1, 1991 (prior art under 35 U.S.C. § 102(e)                
          based on its August 18, 1987, filing date), in view of the                  
          teachings of Radhakrishnan, U.S. 4,906,476, patented March 6,               
          1990 (prior art under 35 U.S.C. § 102(e) based on its December              
          14, 1988, filing date), and McGregor et al. (McGregor), U.S.                
          5,079,234, patented January 7, 1992 (prior art under 35 U.S.C.              
          § 102(e) based on its March 23, 1989, filing date).  All of the             
          claims “stand or fall together” (Appeal Brief, page 3; Examiner’s           
          Answer, page 2).                                                            
               Representative Claim 1 reads:                                          
                    1.   A method of treating a systemic infection which              
               is localized at a site other than the fixed macrophages                
               residing in the liver or the spleen, comprising                        
                    administering to the subject, by intravenous                      
               injection, a composition of liposomes (i) composed of                  
               vesicle-forming lipids, including 1-35 mole percent of a               
               diacyl-chain amphipathic vesicle-forming lipid derivatized             
               with polyethylene glycol having a molecular weight between             
               about 350 and 5,000 daltons (ii) having a selected mean                
               particle diameter in the size range between about 0.07-                
               0.20 microns, and (iii) containing in liposome-entrapped               
               form, a therapeutic compound effective against the source              
               of the infection, and                                                  
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