Ex Parte Wood et al - Page 2

                 Appeal 2007-2212                                                                                        
                 Application 10/667,472                                                                                  
                        Representative claim follows.                                                                    
                        10.  A nanoparticulate composition comprising:                                                   
                 (a) beclomethasone dipropionate particles having an average particle size of                            
                 less than about 1000 nm; and                                                                            
                 (b) at least one surface modifier.                                                                      

                 Cited References:                                                                                       
                        Liversidge   US 5,145,684   Sep. 8, 1992                                                         
                        Lacy et al., Drug Information Handbook (LEXI- Comp, Inc.),                                       
                        pp. 95-96 (1993). (Drug)                                                                         

                 Grounds of Rejection                                                                                    
                        Claims 10-22 and 24-26 stand rejected under 35 U.S.C. § 103(a) as                                
                 obvious over Liversidge in view of Drug.  We select claim 10 as                                         
                 representative of the claims before us as Appellant has not separately argued                           
                 individual claims of the rejection.  37 C.F.R. 41.37(c)(1)(vii) (2006).                                 

                                                    DISCUSSION                                                           
                 Background                                                                                              
                        Delivery of therapeutic agents to the respiratory tract is important for                         
                 both local and systemic treatment of disease.  (Specification 1.)  With                                 
                 conventional techniques, delivery of agents to the lung is extremely                                    
                 inefficient.  (Id.)  Attempts to develop respirable aqueous suspensions of                              
                 poorly soluble compounds have been unsuccessful. (Id.)  Micronized                                      
                 therapeutic agents suspended in aqueous media are too large to be delivered                             
                 by aerosolized aqueous droplets.  (Id.)  With conventional processes, it is                             
                 estimated that only about 10 to 20% of the agent reaches the lung.  (Id.)                               



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