Ex Parte GLASSMAN et al - Page 3




            Appeal No. 1997-1842                                                                              
            Application 08/068,878                                                                            



            Lepor et al. (Lepor 1992), “The Safety, Efficacy and Compliance of Terazosin Therapy              
            for Benign Prostatic Hyperplasia,” J. Urology, 147, pp. 1554-57 (June 1992).                      
                   The references relied upon by this merits panel are set forth above and the                
            following:                                                                                        
            “HYTRIN®,“ in Physicians’ Desk Reference®, 526-28 (45th ed., New Jersey, publisher                
            Edward R. Barnhart, 1991).                                                                        
            Roteman                          4,251,532                 Feb. 17, 1981                          
            Kyncl et al. (Kyncl)             5,212,176                 May 18, 1993                           
                                                                (filed June 29, 1990)                         

                   Claims 1-7 stand rejected under 35 U.S.C. § 103.  The examiner relies upon                 
            Lepor et al. 1988, Lepor et al. 1989, Lepor et al. 1992, Lepor 1989, Dunzendorfer and             
            Fabricius as evidence of obviousness.  We vacate the examiner’s rejection and enter a             
            new ground of rejection under the provisions of 37 CFR § 1.196(b).                                
                                               DISCUSSION                                                     
                   Claim 1 and claims which depend from claim 1 are directed to a method for the              
            chronic treatment, for a period of at least two and one-half years, of urinary symptoms           
            associated with benign prostatic hyperplasia (BPH).   The method comprises the step of            
            administering to a male human patient in need of such treatment a therapeutically                 
            effective amount of 1-(4-amino-6,7-dimethoxy-2-quinazolinyl)-4-[(tetrahydro-2-                    
            furanyl)carbonyl]piperazine or a pharmaceutically-acceptable salt thereof.                        


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