Ex Parte Taneri et alDownload PDFBoard of Patent Appeals and InterferencesApr 13, 201111260697 (B.P.A.I. Apr. 13, 2011) Copy Citation UNITED STATES PATENT AND TRADEMARK OFFICE __________ BEFORE THE BOARD OF PATENT APPEALS AND INTERFERENCES __________ Ex parte JIM TANERI, YI HSIN CHANG, RAFAEL AKYUZ, and SUSAN GOLDSBERRY __________ Appeal 2010-012041 Application 11/260,697 Technology Center 1600 __________ Before TONI R. SCHEINER, DEMETRA J. MILLS, and JEFFREY N. FREDMAN, Administrative Patent Judges. FREDMAN, Administrative Patent Judge. DECISION ON APPEAL This is an appeal under 35 U.S.C. § 134 involving claims to a method of preparing a body surface for epilation. The Examiner rejected the claims as obvious. We have jurisdiction under 35 U.S.C. § 6(b). We affirm. Appeal 2010-012041 Application 11/260,697 2 Statement of the Case Background According to the Specification, it “has surprisingly been discovered that, prior to epilation, by applying a composition that includes a fluid vehicle and is adapted to leave a powder residue on the skin and hair, one or more of hair removal, pain mitigation, and convenience of cleanup are improved” (Spec. 1, ll. 29-32). The Claims Claims 1-6 and 9-23 are on appeal. Independent claims 1 and 21 are representative and read as follows: 1. A method of preparing a body surface for epilation, said method comprising prior to said epilation, applying to said body surface a composition that is adapted to leave a powder residue on said body surface, wherein said composition comprises from about 3% by weight to about 60% by weight of a powder residue generating material and a fluid vehicle. 21. A method of epilating a body surface, said method comprising: applying to said body surface a composition that is adapted to leave a powder residue on said body surface, wherein said composition comprises a water-insoluble solid and a fluid vehicle; and epilating said body surface after said composition is allowed to dry. Appeal 2010-012041 Application 11/260,697 3 The issue The Examiner rejected claims 1-6 and 9-23 under 35 U.S.C. § 103(a) as obvious over Marron 1 and Kaleta 2 (Ans. 3-6). The Examiner finds that “Marron discloses a numbing gel composition used in preparation for a body hair removal procedure, such as the hot wax method (abstract, lines 1-2), and the composition taught is a pain blocker composition that comprises lidocaine to reduce the pain associated with the body hair removal” (id. at 4). The Examiner finds that Kaleta “discloses oil-in-water compositions useful for topical application to the human skin that have an aesthetically pleasing skin feel and are also useful for delivering a wide variety of active ingredients . . . Kaleta et al. also teaches the formulation for the delivery of anesthetic agents such as lidocaine” (id.). The Examiner finds that Kaleta “is silent as to whether the ingredients present in the taught composition will generate a powder residue, and whether the composition is adapted to generate a powder residue on the body” (id.). The Examiner finds that “one of ordinary skill in the art would expect that a powder residue would necessarily form from the use of the formulation taught by Kaleta” (id. at 4-5). Appellants contend that “one skilled in the art could not expect to preserve the low viscosity that appears to be required in Marron‟s gel, while somehow incorporating Kaleta‟s emulsion (which appears to have, at minimum a viscosity that is ten times as much)” (App. Br. 4-5). Appellants 1 Marron, US 2004/0077593 A1, published Apr. 22, 2004. 2 Kaleta et al., US 5,618,522, issued Apr. 8, 1997. Appeal 2010-012041 Application 11/260,697 4 contend that one “skilled in the art would reasonably conclude that these two systems would not be compatible with one another. Alternatively, one skilled in the art would reasonably conclude that in order to somehow force them to be compatible, one would expect to lose the pleasant skin feel advantages of Kaleta” (App. Br. 5). Appellants contend that if one were to somehow combine these dissimilar compositions, that one would still not have a composition that includes from about 3% by weight to about 60% by weight of a powder residue generating material as required in independent claim 1. Furthermore, there is no teaching or suggestion within either of these references to adjust the amount of powder generating residue to within Applicant's claimed range. (Id.) Appellants contend that the “Office has failed to show a reason for one skilled in the art, faced with countless possible skin care formulations, each with various benefits as well as tradeoffs, to substitute the emulsions of Kaleta for the numbing gels of Marron” (id.). The issue with respect to this rejection is: Does the evidence of record support the Examiner‟s conclusion that Marron and Kaleta render claims 1 and 21 obvious? Findings of Fact 1. The Specification teaches that in “order to ensure that the composition is adapted to leave a residue, the composition includes a powder residue-generating material. Suitable powder residue-generating Appeal 2010-012041 Application 11/260,697 5 materials include water-insoluble solids, water-soluble salts, and combinations thereof” (Spec. 3, ll. 6-8). 2. The Specification teaches that one “example of a suitable water-insoluble solid includes inorganic particulates, such as . . . silicates . . . Particularly preferred examples of inorganic particles include silicon oxides” (Spec. 3, ll. 19-25). 3. The Specification teaches that “the powder residue-generating material is present in the composition in a weight percentage relative to the total composition of at least about 1%” (Spec. 3, ll. 11-13). 4. Marron teaches that there “is a need for an effective, economical, topical, anesthetic composition for assisting in the field of human body hair removal” (Marron 1 ¶ 0004). 5. Marron teaches “a topical anesthetic gel composition comprising lidocaine, tetracaine, methylcellulose, and normal saline solution for reducing pain associated with human body hair removal” (Marron 1 ¶ 0002). 6. Kaleta teaches an “oil-in-water emulsion compositions useful for topical application to human skin. These compositions have an aesthetically pleasing skin feel and are also useful for delivering a wide variety of active ingredients to the skin” (Kaleta, col. 1, ll. 6-10). 7. Kaleta teaches an “an oil-in-water emulsion composition useful for topical application to human skin comprising: (a) from about 5% to about 60% by weight of the total composition of an oil phase . . . (i) from about 0.1% to about 10% by weight of the total composition of a particulate Appeal 2010-012041 Application 11/260,697 6 thickener selected from the group consisting of silica, treated silica” (Kaleta, col. 2, l. 55 to col. 3, l. 1). 8. Kaleta teaches that the composition may comprise “from 0% to about 10% by weight of the total composition of an aqueous phase emulsifier” (Kaleta, col. 3, ll. 14-15). 9. Kaleta teaches that the “oil phase comprises from about 0.1% to about 10% by weight of the total composition of a particulate thickener selected from the group consisting silica, treated silica . . . Silica is also known as silicon dioxide” (Kaleta, col. 5, ll. 38-55). 10. Kaleta teaches that “[a]nesthetic actives preferred for inclusion in compositions of the present invention include pharmaceutically- acceptable salts of lidocaine” (Kaleta, col. 11, ll. 13-15). Principles of Law “The combination of familiar elements according to known methods is likely to be obvious when it does no more than yield predictable results.” KSR Int’l Co. v. Teleflex Inc., 550 U.S. 398, 416 (2007). “If a person of ordinary skill can implement a predictable variation, § 103 likely bars its patentability.” Id. at 417. Where … the claimed and prior art products are identical or substantially identical, or are produced by identical or substantially identical processes, the PTO can require an applicant to prove that the prior art products do not necessarily or inherently possess the characteristics of his claimed product. Whether the rejection is based on “inherency” under 35 U.S.C. § 102, on “prima facie obviousness” under 35 U.S.C. § 103, jointly or alternatively, the burden of proof is the same, and its fairness is evidenced by the PTO's inability to manufacture products or to obtain and compare prior art products. Appeal 2010-012041 Application 11/260,697 7 In re Best, 562 F.2d 1252, 1255 (CCPA 1977). Analysis Marron teaches that hair removal may be painful, and suggests application of an anesthetic composition to skin prior to human body hair removal (FF 4-5). Kaleta teaches a topical composition with “an aesthetically pleasing skin feel and are also useful for delivering a wide variety of active ingredients to the skin” (Kaleta, col. 1, ll. 6-10; FF 6). Kaleta teaches that the composition may comprise up to 10% of silica as well as lidocaine (FF 7-10). Applying the KSR standard of obviousness to the findings of fact, we agree with the Examiner that it would have been obvious to apply the topical composition of Kaleta prior to human body hair removal as suggested by Marron, in order to minimize pain with an aesthetically pleasing skin feel (FF 4-10). Such a combination is merely a “predictable use of prior art elements according to their established functions.” KSR, 550 U.S. at 417. Appellants contend that “one skilled in the art could not expect to preserve the low viscosity that appears to be required in Marron‟s gel, while somehow incorporating Kaleta‟s emulsion (which appears to have, at minimum a viscosity that is ten times as much)” (App. Br. 4-5). Appellants contend that one “skilled in the art would reasonably conclude that these two systems would not be compatible with one another. Alternatively, one skilled in the art would reasonably conclude that in order to somehow force them to be compatible, one would expect to lose the pleasant skin feel advantages of Kaleta” (id. at 5). Appeal 2010-012041 Application 11/260,697 8 We are not persuaded. This argument of Appellants‟ mischaracterizes the rejection. The Examiner‟s rejection does not suggest mixing or combining the compositions of Kaleta and Marron. Instead, the Examiner suggests that “it would have been prima facie obvious to one of ordinary skill in the art at the time the invention was made to have used the emulsion formulation taught by Kaleta et al. to deliver lidocaine” (Ans. 5). The Examiner relies upon Marron to suggest a reason to deliver the lidocaine comprising composition of Kaleta to a person about to undergo hair removal (FF 5). Appellants contend that if one were to somehow combine these dissimilar compositions, that one would still not have a composition that includes from about 3% by weight to about 60% by weight of a powder residue generating material as required in independent claim 1. Furthermore, there is no teaching or suggestion within either of these references to adjust the amount of powder generating residue to within Applicant's claimed range. (App. Br. 5.) We are not persuaded. Appellants‟ Specification teaches that powder generating materials may include silicates and silicon oxides (FF 1-3). Kaleta teaches that the composition may comprise “from about 0.1% to about 10% by weight of the total composition of a particulate thickener selected from the group consisting of silica, treated silica” (Kaleta, col. 2, l. 55 to col. 3, l. 1; FF 7). So Kaleta teaches incorporation of silica, which Appellants own Specification acknowledges is a powder generating material (FF 1-3, 7-9). With regard to the range, Kaleta‟s range of 0.1% to about Appeal 2010-012041 Application 11/260,697 9 10% for silica significantly overlaps the claimed range of “3% by weight to about 60% by weight of a powder generating material” 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.) Appellants contend that the “Office has failed to show a reason for one skilled in the art, faced with countless possible skin care formulations, each with various benefits as well as tradeoffs, to substitute the emulsions of Kaleta for the numbing gels of Marron” (App. Br. 5). We are not persuaded. The Examiner provided a very specific reason why “the skilled artisan would use the emulsion formulation disclosed by Kaleta et al. (the aesthetically pleasing skin feel)” (Ans. 8). Appellants contend that the “Examiner has not however shown after use thereof there would be a reasonable expectation of successfully epilating the skin” (App. Br. 5). We are not persuaded by the reasonable expectation of success argument. Marron demonstrates successful use of a lidocaine containing composition prior to epilation to anesthetize the skin (FF 4-5). Kaleta teaches skin treating compositions which are aesthetically pleasing and which contain lidocaine as an active ingredient (FF 6-10). Kubin stated that “[r]esponding to concerns about uncertainty in the prior art influencing the purported success of the claimed combination, this court [in O’Farrell] stated: „[o]bviousness does not require absolute predictability of success … all that is required is a reasonable expectation of success.”‟ In re Kubin, 561 F.3d 1351, 1360 (Fed. Cir. 2009) (citing In re O’Farrell, 853 F.2d 894, 903- Appeal 2010-012041 Application 11/260,697 10 904 (Fed. Cir. 1988)). Appellants have provided no evidence that Kaleta‟s lidocaine containing composition would not have been reasonably expected to function to anesthetize skin prior to epilation, and we agree with the Examiner that “the skilled artisan would expect both formulations to have the same effect (anesthetizing the skin) as both formulations contain the same active ingredient” (Ans. 8). Conclusion of Law The evidence of record supports the Examiner‟s conclusion that Marron and Kaleta render claims 1 and 21 obvious. SUMMARY In summary, we affirm the rejection of claims 1 and 21 under 35 U.S.C. § 103(a) as obvious over Marron and Kaleta. Pursuant to 37 C.F.R. § 41.37(c)(1)(vii)(2006), we also affirm the rejection of claims 2-6, 9-20, 22, and 23, as these claims were not argued separately No time period for taking any subsequent action in connection with this appeal may be extended under 37 C.F.R. § 1.136(a)(1). AFFIRMED JNF cdc Copy with citationCopy as parenthetical citation