Appeal No. 2001-1221 Page 2 Application No. 08/442,957 According to the examiner (Answer, page 4) Teutsch [teaches] a genus of 19-nor steroid compounds having a keto group in the 3-position and double bonds in the 4 and 9 positions and a substituted phenyl group at the 11-position (cols. 1-6). The 11-phenyl group of the compounds are substituted with an alkynyl group of 2 to 8 carbon atoms which may be substituted with a hydroxy group (col. 1, lines 43-47). The 17-position substituents include those of the claims (col. 2). The compounds are taught to have antiprogestomimetic and antiglucocorticoid activities. Similarly (id., page 5) Loozen teaches a genus of 19-nor steroid compounds having a keto group in the 3-position and double bonds in the 4 and 9 positions. The compounds have a homocyclic or heterocyclic aryl group in the 11- position substituted with a hydrocarbon group of 1-10 carbon atoms which is substituted with oxo and/or hydroxyl groups (col. 1 to col. 2, line 9). The compounds are taught to have antiprogestinic activity (Col. 1, lines 27-29). Further according to the examiner (id., pages 4, 5, and 6), each of the claims differs from the prior art by reciting a more limited genus than the reference having an organic radical, which may be arylene, attached to the 11-position through a carbon atom which terminates in a CH2OH group. However, it would have been obvious to one having ordinary skill in the art at the time of the invention to select any of the species of the genus taught by the reference, including those of the claims having the hydroxy group attached to the terminal carbon of the 11-position substituent, because an ordinary artisan would have the reasonable expectation that any of the species of the genus would have similar properties and, thus, the same use as the genus as a whole. There would appear to be no dispute that the claimed species and subgenus are encompassed by the generic 19-nor steroid formulas described in Teutsch and Loozen. Nevertheless, without conceding that the claimed compounds would have been prima facie obvious over the prior art, appellants argue that the references Adescribe final products which have a particular pharmacological activity which is completely non- analogous to Applicants= pharmacological activity,@ thus, Athe decision of [In re Magerlein, 602 F.2d 366, 202 USPQ 473 (CCPA 1979)] is pertinent to the presentPage: Previous 1 2 3 4 5 6 NextLast modified: November 3, 2007