Appeal No. 2004-1790 Page 6 Application No. 09/836,971 Appellants argue that “Crowson has a critical and fatal flaw. Crowson exposes HT 29 colorectal cancer cells, in vitro, to various agents. There is not one word concerning administration of the agents to a mammal as explicitly claimed by the Appellants.” Appeal Brief, pages 9-10 (emphasis in original). We agree. In order for a prior art reference to serve as an anticipatory reference, it must disclose every limitation of the claimed invention, either explicitly or inherently. See In re Schreiber, 128 F.3d 1473, 1477, 44 USPQ2d 1429, 1432 (Fed. Cir. 1997). The examiner asserts that “Crowson discloses that HT29 colorectal cells are of known malignancy and PEG inhibits the growth of HT29 cancer cell lines,” arguing that “it is implicit that PEG is effective in treating or inhibiting colon or rectal cancer.” That is not, however, explicit or inherent teaching of administering the PEG to a mammal, thus Crowson fails to teach every limitation of the claimed invention, and the rejection is reversed. 3. Rejection under 35 U.S.C. § 103(a) Claims 9-11 and 15-19 stand rejected under 35 U.S.C. § 103(a) as being obvious over Crowson. The rejection is set forth below. Crowson [ ] (described above) teaches the use and efficacy of several cytocidal and bowel preparation agents such as PEG, cetrimide, povidone iodine, etc. Crowson shows that the compounds are capable of killing colorectal cell lines with different efficacies and concludes that only cetrimide is capable of completely killing the cells. However, the instant claims do not mention the amount of therapeutic activity desired. Besides, PEG still exhibits about 30 to 40% activity, which is considered to be significant. Further, the results in table Iv [sic] shows [sic] that the activity is varies [sic] with the compounds as well as incubation time. Accordingly depending on the amount of activity desired, a skilled artisan would be able to use PEG of Crowson, for different time intervals with an expectation to achieve the desiredPage: Previous 1 2 3 4 5 6 7 8 9 NextLast modified: November 3, 2007