Appeal No. 2004-1188 Page 2 Application No. 09/940,784 weight about 360,000; and a water-soluble polyethylene glycol; the total concentration of the linear polymer ingredients being about 0.5 to about 15 percent by weight/volume. The references relied upon by the examiner are: Shimizu et al. (Shimizu) 4,728,509 Mar. 1, 1988 Parnell 5,015,474 May 14, 1991 Gilbert et al. (Gilbert) 5,116,847 May 26, 1992 Rybacki et al. (Rybacki), “Auxiliary Substances in Technology of Drug Form,” Library of a Pharmicist, Vol. 7, pp. 1-12 (1980) GROUNDS OF REJECTION Claims 15-17 and 21-28 stand rejected under 35 U.S.C. § 103 as being unpatentable over the combination of Shimizu, Gilbert and Parnell. Claims 18-20 and 29-33 stand rejected under 35 U.S.C. § 103 as being unpatentable over the combination of Shimizu, Gilbert and Parnell, further in view of Rybacki. We reverse. DISCUSSION The combination of Shimizu, Gilbert and Parnell: According to the examiner (Answer, page 3), Shimizu disclose an aqueous nasal spray composition comprising, inter alia, a drug and polyvinylpyrrolidone (PVP) having an average molecular weight of about 25,000- 120,000 daltons. The examiner recognizes, however, that Shimizu does not teach the (1) use of two or more PVPs having different average molecular weights, or (2) oxymetazoline hydrochloride. Answer, page 4. The examiner relies on Gilbert and Parnell to make up these deficiencies.Page: Previous 1 2 3 4 5 6 7 NextLast modified: November 3, 2007