Appeal No. 2001-1051 Page 3 Application No. 08/185,079 According to the rejection: This deficiency is cured by the similarity between the respiratory syncytial virus (RSV) and the AIDS etiological agent. RSV and HIV are both RNA viruses possessing a similar replicative schema in their respective host cells. It is noted that Tidwell [ ] reported the claimed compounds exhibiting antiviral activity to virus other that [sic] the claimed RSV (([Tidwell III]), column 11, lines 43-45). Vonderfecht [ ] further motivate[s] the skilled artisan to employ these compounds therapeutically on retroviral infection. Attention is directed to page 2015 wherein Vonderfecht [ ] suggest[s] these compounds as useful for the claimed retroviral etiological agent. Absent information to the contrary, the skilled artisan would have been motivated by the data of Tidwell [ ] to employ the claimed compounds against various RNA virus and enjoy a reasonable expectation of success. Although Tidwell [ ] report[s] that the claimed compounds are specific for the RSV etiologial agent, the statement at column 11 and the presented data render such averments moot. Thus, two distinct and powerful motivations [exist] [sic] to employ Applicants’ compounds in retroviral therapy. It would follow therefore that the instant claims recite prima facie obvious subject matter, and are properly rejected under 35 USC 103. Id. at 3-4. Appellants argue that the Tidwell references are all cumulative to one another, and all deal with the RSV virus. According to Appellants, RSV is not a retrovirus, but a paramyxovirus and that paramyxovirus and its replicative scheme is not analogous to that of a retrovirus. Vonderfecht, Appellants argue, relates to a rotavirus, which again, is not a retrovirus. Moreover, Appellants contend that, contrary to the statement in the rejection that the claimed compounds are useful against retroviruses, “Vonderfecht only states that a number of viruses require host proteases for productive infection and that therefore protease inhibitors MAY have a broad range of antiviral activity.”Page: Previous 1 2 3 4 5 6 7 8 NextLast modified: November 3, 2007