Ex Parte Zelkha et alDownload PDFPatent Trials and Appeals BoardJan 23, 201913137061 - (D) (P.T.A.B. Jan. 23, 2019) Copy Citation UNITED STA TES p A TENT AND TRADEMARK OFFICE APPLICATION NO. FILING DATE 13/137,061 07/18/2011 23117 7590 01/25/2019 NIXON & V ANDERHYE, PC 901 NORTH GLEBE ROAD, 11 TH FLOOR ARLINGTON, VA 22203 FIRST NAMED INVENTOR Morris Zelkha UNITED STATES DEPARTMENT OF COMMERCE United States Patent and Trademark Office Address: COMMISSIONER FOR PATENTS P.O. Box 1450 Alexandria, Virginia 22313-1450 www .uspto.gov ATTORNEY DOCKET NO. CONFIRMATION NO. GPK-6278-4 8408 EXAMINER KIM, JENNIFER M ART UNIT PAPER NUMBER 1628 NOTIFICATION DATE DELIVERY MODE 01/25/2019 ELECTRONIC Please find below and/or attached an Office communication concerning this application or proceeding. The time period for reply, if any, is set in the attached communication. Notice of the Office communication was sent electronically on above-indicated "Notification Date" to the following e-mail address(es): PTOMAIL@nixonvan.com pair_nixon@firsttofile.com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte MORRIS ZELKHA, RACHEL LEVY, ESTHER P ARAN, YOA V SHARON!, and JOSEPH LEVY Appeal2018-001897 Application 13/137,061 1 Technology Center 1600 Before RICHARD M. LEBOVITZ, JEFFREY N. FRED MAN, and ELIZABETH A. LA VIER, Administrative Patent Judges. LA VIER, Administrative Patent Judge. DECISION ON APPEAL Pursuant to 35 U.S.C. § 134(a), Appellants seek review of the Examiner's rejection of claims 1, 15-17, 25, and 26. We have jurisdiction under 35 U.S.C. § 6(b ). For the reasons set forth below, we AFFIRM. BACKGROUND The Specification describes compositions combining polyphenols and carotenoids, which may be useful in the inhibition of inflammatory mediators. See Spec. 1. Claim 1 is illustrative, and recites: 1 Appellants identify Lycored, Ltd., as the real party in interest. Br. 3. Appeal2018-001897 Application 13/137 ,061 1. A therapeutic composition comprising curcumin, and lutein and lycopene combined in the following weight ranges: Lycopene: Lutein: Curcumin, 0.1-1.5: 0.1-1.5: 0.1-1.0. Br. 11 (Claims Appendix) (some formatting added). REJECTION MAINTAINED ON APPEAL Claims 1, 15-17, 25, and 26 stand rejected under 35 U.S.C. § I03(a) (pre-AIA) as unpatentable over Nishino, 2 Stahl, 3 and Sharoni. 4 Ans. 2. DISCUSSION As relevant to illustrative claim 1, the Examiner relies on Nishino as teaching compositions including, inter alia, lycopene, lutein, and curcumin. See Final Action 4 ( citing Nishino,r,r 104, 5 105 and Example 1 ). The Examiner notes that although Example 1 ofNishino provides for lycopene: lutein: curcumin in a 1: 0.6: 10 ratio (id.), Nishino also discloses that "the amount of curcumin can be employed approximately 5 to 250 parts by weight (particularly about 10-100 parts by weight) per 100 parts by weight 2 Nishino et al., US 2004/0116514 Al, published June 17, 2004. 3 Stahl et al., Carotenoid Mixtures Protect Multilamellar Liposomes against Oxidative Damage: Synergistic Effects of Lycopene and Lutein, 427 FEBS LETTERS 305 (1998). 4 Sharoni et al, US 2004/0259959 Al, published Dec. 23, 2004. 5 The Examiner cites to paragraph "140" ofNishino rather than paragraph 104, as we have cited here. As Nishino does not include a paragraph 140, we presume the Examiner meant to cite paragraph 104, which, along with paragraph 105, constitutes Nishino's Example 1. 2 Appeal2018-001897 Application 13/137 ,061 of carotenoid compounds" (id. (citing Nishino ,r 75)). Nishino lists lycopene and lutein among its examples of carotenoid compounds. See Nishino ,r 48. Therefore, Nishino's ratio ranges of carotenoids:curcumin overlap with the ratio ranges of lycopene:lutein:curcumin recited in claim 1. See Final Action 4. This alone constitutes a prima facie case of obviousness of claim 1. See In re Peterson, 315 F.3d 1325, 1329 (Fed. Cir. 2003) ("In cases involving overlapping ranges, we and our predecessor court have consistently held that even a slight overlap in range establishes a prima facie case of obviousness."); see also In re Aller, 220 F.2d 454, 456-58 (CCPA 1955) ("[W]here the general conditions of a claim are disclosed in the prior art, it is not inventive to discover the optimum or workable ranges by routine experimentation."). However, the Examiner further supports the rejection through reference to Stahl, for the synergistic effect of lycopene and lutein. See Final Action 5 ( citing Stahl 307, Title). 6 The Examiner finds it would have been obvious to combine the references by optimizing the amount of curcumin in Nishino 's Example 1 to curcumin levels within the claimed range, because it would be a matter of discovering optimal or workable ranges, well within the abilities of the ordinarily skilled artisan. See id. at 5- 6 ( citing Aller). Appellants do not dispute the Examiner's specific findings regarding the individual elements of claim 1. See generally Br. 6-9. Instead, 6 The Examiner also cites to Sharoni, as teaching that lycopene, or lycopene and additional carotenoids, can enhance the inhibitory effects of phytoene and phytofluene on mammary cancer cell proliferation. See Final Action 5 ( citing Sharoni Abstract, ,r,r 8, 25). These teachings are relevant to certain dependent claims, which recite phytoene and/or phytofluene. 3 Appeal2018-001897 Application 13/137 ,061 Appellants assert that their claims embody a previously-unappreciated insight, i.e., that "curcumin at certain levels ( e.g. as defined by the ratio between the carotenoids and curcumin) results in a previously entirely unknown - and previously unexpected - synergistic interaction with certain carotenoids, leading to unexpectedly high levels of inhibition of the production of some key anti-inflammatory mediators." Id. at 6. Therefore, according to Appellants, the teachings of synergism between carotenoids cited by the Examiner would not have motivated the ordinarily skilled artisan to optimize curcumin levels to achieve the claimed ranges. See id. at 8; see also id.at 9. In support, Appellants point to Figures 13A, 13B, and 14 of the drawings filed with the Specification, which Appellants assert show a "marked synergism" when lycopene, lutein, and curcumin are used in combination, as compared to the additive effect one would expect from summing the results for each component individually. Id. at 8 ( discussing Figs. 13A, 13B); see also id. at 9 (discussing Fig. 14). Having reviewed Appellants' Figures 13A, 13B, and 14, we conclude that Appellants' proffered evidence of unexpected results are not entitled to substantial weight. Figure 14 is reproduced below: 4 Appeal2018-001897 Application 13/137 ,061 :fig. 14 60·1 i ! 50~ .: 1 :.i 40~ .:.! l .! 30- CurcuminPC l 20~ 1~]____._ __ ~----···-.---..._L...,._._ Cur-,:;vmml'C ZµM + LycOmcto 1 µ.M lutein 1µM 60· 50· 40 + Pure Curcum in o +, ...,.J..m.=.,:;i'' :............., _ ___._..__,...--1'""--J--~ Cvr-.::1,ul!tin 2µM LyeOmcto 1 i.J,1 l U1t,i11 1 µht + + + + • + s s + + + + + + s s Figure 14 is a pair of bar graphs demonstrating the percentage of nitrous oxide (NO) inhibition observed in the presence of curcumin, lycopene, or lutein alone (first three bars, both graphs), curcumin and lycopene together (fourth bar, both graphs), and curcumin, lycopene, and lutein together (last 5 Appeal2018-001897 Application 13/137 ,061 bar, both graphs). 7 The "S" indicates what Appellants calculate to constitute synergistic inhibition. See Spec. 50. As illustrated by (but not limited to) Figure 14 of the Specification, Appellants' data do not include a comparison with the combination already known in the prior art as having synergistic effects, i.e., lycopene and lutein together. See, e.g., Stahl Abstract; Sharoni ,r 8. Nor did Appellants compare their combination(s) to the composition of Example 1 ofNishino, to show that claimed ratio had unexpected advantages while the composition of Nishino having all three components did not. See Ans. 4. Without such a comparison, a determination cannot be made as to whether the synergistic effects reported in the Specification and Figures 13A, 13B, and 14 are due to the combination of lycopene and lutein, to the addition of curcumin to the already-known-to-be-synergistic lycopene/lutein combination, or, as Appellants maintain, to the specifically claimed ratios of lycopene: lutein: curcumin. Thus, we agree with the Examiner's general finding that Appellants have failed to compare their invention to the closest prior art. See Ans. 4. Having considered Appellants' arguments, we are not persuaded of any reversible error by the Examiner in rejecting claim 1. Appellants do not separately argue claims 15-17, 25, or 26; these fall with claim 1. See 37 C.F.R. § 4I.37(c)(l)(iv). 7 "Curcumin-PC" is a commercially available curcumin preparation with improved miscibility. See Spec. 8. "Curcumin" refers to pure curcumin. See id. at 50. "Lycomato" is a commercially available tomato extract, used as a source of lutein. See id. at 8, 16. 6 Appeal2018-001897 Application 13/137 ,061 CONCLUSION We sustain the Examiner's rejection of claims 1, 15-17, 25, and 26. No time period for taking any subsequent action in connection with this appeal may be extended under 3 7 C.F .R. § 1.13 6( a)( 1 )(iv). AFFIRMED 7 Copy with citationCopy as parenthetical citation