Ex Parte Owen et alDownload PDFPatent Trial and Appeal BoardMar 18, 201911920632 (P.T.A.B. Mar. 18, 2019) Copy Citation UNITED STA TES p A TENT AND TRADEMARK OFFICE APPLICATION NO. FILING DATE FIRST NAMED INVENTOR 11/920,632 12/21/2007 Richard Harley Grenville Owen 22428 7590 03/20/2019 Foley & Lardner LLP 3000 K STREET N.W. SUITE 600 WASHINGTON, DC 20007-5109 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. 093840-0102 8592 EXAMINER EISEMAN, ADAM JARED ART UNIT PAPER NUMBER 3791 NOTIFICATION DATE DELIVERY MODE 03/20/2019 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): ipdocketing@foley.com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte RICHARD HARLEY GRENVILLE OWEN, STEPHEN BLATCHER, STEWART MADDISON FOX, and MARTIN LAWRENCE HUGHES Appeal2017-006668 Application 11/920,632 Technology Center 3700 Before BENJAMIN D. M. WOOD, ANNETTE R. REIMERS, and SEAN P. O'HANLON, Administrative Patent Judges. O'HANLON, Administrative Patent Judge. DECISION ON APPEAL STATEMENT OF THE CASE Richard Harley Grenville Owen et al. ("Appellants") 1 appeal under 35 U.S.C. § 134(a) from the Examiner's decision, as set forth in the Final Office Action mailed March 24, 2016 ("Final Act."), rejecting claims 57-75, 1 The Appeal Brief identifies PlaqueTec Limited as the real party-in-interest. Appeal Br. 2. Appeal2017-006668 Application 11/920,632 92-96, 101, and 102 (all pending claims). Appellants' representative presented oral argument on March 7, 2019. We have jurisdiction over this appeal under 35 U.S.C. § 6(b). We AFFIRM-IN-PART. SUMMARY OF THE INVENTION The claimed subject matter "relates to a catheter for insertion into a blood vessel allowing blood samples to be taken." Spec. 1. Claims 57, 72, and 92 are independent. Claims 57 and 92, reproduced below from pages 27 and 31 (Claims Appendix), respectively, of the Appeal Brief, are illustrative of the claimed subject matter: 57. A catheter device for insertion into a blood vessel, compnsmg: a sampling part arranged to collect and preserve a plurality of spatially separated discrete blood samples from a plurality of locations along a length of the blood vessel; wherein the sampling part includes: an axially elongated sample member having an axial array of a plurality of openings for receiving blood from outside of the catheter device at intervals along the length of the blood vessel; and an elongated sleeve coaxial with the sample member, the sleeve defining an axial passage for housing the sample member and including a plurality of through holes corresponding to said openings in the sample member, and wherein movement between the sleeve and the sample member aligns all the through holes with the openings of the sample member, to simultaneously expose all the openings to blood outside the catheter device so as to collect the plurality of discrete blood samples along the length of the blood vessel, and wherein the catheter device is flexible so as to be channeled through the blood vessel, and has a blunt distal end. 92. A method for positioning a catheter in a blood vessel, compnsmg: 2 Appeal2017-006668 Application 11/920,632 providing the catheter having a sampling part and a reference guide sleeve, the catheter being flexible so as to be channeled through the blood vessel, and having a blunt distal end· ' introducing said reference guide sleeve into the blood vessel at a fixed position relative to the blood vessel, wherein said reference guide sleeve has an axial duct for receiving the sampling part of said catheter; and collecting a plurality of spatially separated discrete blood samples from a plurality of locations along a length of the blood vessel, wherein the reference guide sleeve and sampling part have one or more indexing parts with respect to each other, which positions the sampling part at a predetermined position relative to the reference guide. REFERENCES The Examiner relies on the following prior art references in rejecting the claims on appeal: Kreuzer Martin Barbut Sutton Brown us 4,808,158 us 5,472,417 us 6,165,199 US 7,179,232 B2 WO 2004/010874 Al REJECTIONS Feb.28, 1989 Dec. 5, 1995 Dec. 26, 2000 Feb.20,2007 Feb. 5,2004 I. Claims 101 and 102 stand rejected under 35 U.S.C. § 112, second paragraph, as being indefinite. II. Claims 57----62, 65-75, and 102 stand rejected under 35 U.S.C. § I03(a) as being unpatentable over Brown, Barbut, and Kreuzer. III. Claims 63 and 64 stand rejected under 35 U.S.C. § I03(a) as being unpatentable over Brown, Barbut, Kreuzer, and Martin. 3 Appeal2017-006668 Application 11/920,632 IV. Claims 92-96 and 101 stand rejected under 35 U.S.C. § 103(a) as being unpatentable over Brown, Barbut, Kreuzer, and Sutton. ANALYSIS Rejection I The Examiner determines that "[t]he term 'about' in claims 101 and 102 is a relative term which renders the claim indefinite." Final Act. 2. According to the Examiner, "[t]he [S]pecification does not give any definition to the term about, and as such it is unclear as to what margin of error or tolerance is applied to the claimed ranges, thus leaving the claims indefinite." Id. at 2-3; see also Ans. 13-15. Appellants traverse, arguing that "the term 'about' as recited in claims 101 and 102 should be afforded its plain and ordinary meaning of 'approximately"' and that "those of ordinary skill in the art would have known the approximate volume of a sample needed for a diagnostic chemistry process." Appeal Br. 7, 8 (citing MPEP§ 2173.05(b)(III)). Appellants note that "[t]he term 'about' is routinely used in patent claims, and the courts routinely construe it as plain meaning [sic], accordingly to how 'a person having ordinary skill in the art' would understand it." Reply Br. 3. "[T]he word 'about' does not have a universal meaning in patent claims, and [its] meaning depends on the technological facts of the particular case." Pall Corp. v. Micron Separations, Inc., 66 F.3d 1211, 1217 (Fed. Cir. 1995). Use of the word about as part of a numeric range avoids a strict numerical boundary to the specified parameter. Cohesive Techs. Inc. v. Waters Corp., 543 F.3d 1351, 1368 (Fed. Cir. 2008). In determining the 4 Appeal2017-006668 Application 11/920,632 range encompassed by the term about, one must consider the context of the term as it is used in the specification and claims of the application. Pall, 66 F.3d at 1217. Here, the Specification discusses the sample volume as follows: "Many diagnostic chemistry processes require samples of approximately 50 µ1 and, hence, for many embodiments each discrete sampk is substantialzy of this value. Hmvever, the discrete samples may be behveen 0. 1 µland 100 µl, more preferably behveen 20 J.tl and 50 ~tL~' Spec. 6 (emphases added} Thus, the Specification supports Appellants' assertion that the tenn about as used in the claims means "approximately.'' See Appeal Br. 7; see also Merck & Co. v. Teva Pharms. USA, Inc., 395 F.3d 1364, 1369 (Fed. Cir. 2005) (recognizing the ordinary meaning of about to be approximately). The Examiner appears to apply a per se rule that because the claims include the word about, the claims are indefinite. Such an approach is improper, as it is well established that the use of relative terminology in claim language does not automatically render the claim indefinite. See, e.g., Seattle Box Co., Inc. v. Indus. Crating & Packaging, Inc., 731 F .2d 818, 826 (Fed. Cir. 1984). Rather, the correct test is whether one of ordinary skill in the art would understand what is claimed when the claim is read in light of the specification. Id. As set forth above, one of skill in the art would understand that a "volume ... between about lO~tl and 50j.tl" means a volume between approximately 10 µ1 and 50 µ1; in other words, Appellants' "use of the term 'about' shows that [Appellants] did not intend to limit the claimed ranges to their exact end-points." In re Harris, 409 F.3d 1339, 1343 (Fed. Cir. 2005). 5 Appeal2017-006668 Application 11/920,632 Accordingly, we do not sustain the rejection of claims 101 and 102 as being indefinite. Rejection II Independent claim 57 recites a catheter device "wherein movement between the sleeve and the sample member aligns all the through holes with the openings of the sample member ... so as to collect the plurality of discrete blood samples along the length of the blood vessel." Appeal Br. 27 (Claims App.). Independent claim 72 recites a catheter system "wherein movement between the sleeve and the sample member aligns all the through holes with the openings of the sample member ... so as to collect the plurality of discrete blood samples along the length of the blood vessel." Id. at 29-30. The Examiner relies on Barbut to teach this feature, finding: Barbut teaches a tissue extraction device comprising an elongate extraction member having a plurality of openings for receiving blood from outside the device and an elongate sleeve coaxial with the sample member including a plurality of through holes corresponding to said openings in the extraction/perfusion member and wherein movement between the sleeve and extraction/perfusion member aligns all the through holes with the openings of the sample member, to simultaneously expose all the openings or simultaneously close all openings. Final Act. 4--5 (citing Barbut, 7:23-37, Figs. 6-8). Barbut discloses medical devices for use in treating patients with acute stroke or occlusive cerebrovascular disease. Barbut, 1:7-9. In one embodiment, a catheter includes a lumen having a balloon occluder and an aspiration port at the distal end of the lumen. Id. at 5:66-6:9, Fig. 3. A chopping mechanism is closely associated with the aspiration port. Id. at 6 Appeal2017-006668 Application 11/920,632 6:9-12. The catheter is inserted into the patient's artery such that the balloon occluder is positioned proximate an occlusion in the artery. Id. at 6:23-35, Fig. 4A. The balloon is inflated to create a closed chamber between the balloon and the occlusion, blood is aspirated from the chamber, and the occluding material is removed through application of negative pressure and the chopping mechanism positioned adjacent an aspiration port at the distal end of the catheter. Id. at 6:35---65. In another embodiment of the device, the catheter also includes a perfusion lumen having two concentric cylindrical members, each having perfusion ports therein. Id. at 7:23-35. The perfusion ports are located proximal to the balloon occluder. Id. at 7:23-24, Fig. 6. "The second member can be rotated relative to the first member so that the perfusion ports on the first member align with the perfusion ports on the second member." Id. at 7:35-37. The catheter is inserted into the patient's artery and the balloon occluder is inflated as in the previously discussed embodiment. Id. at 7:38--47. The second member is then rotated relative to the first member to align the perfusion ports, and high pressure flow is released through the perfusion ports. Id. at 7:47-52, 8:7-19. This high pressure flow is directed through collateral arteries to provide improved perfusion to the restricted area. Id. at 7:52-57. As illustrated in Figure 8B, the inflated balloon occluder separates the opposing perfusion and aspiration flows. Thus, as correctly noted by Appellants, Barbut's perfusion ports are not used to collect samples therein. Appeal Br. 17. The Examiner does not rely on Brown or Kreuzer in any manner that would remedy the deficiency noted above with respect to Barbut. The rejection of claims 57 and 72 is, 7 Appeal2017-006668 Application 11/920,632 thus, based on an erroneous factual finding, and the conclusion of obviousness cannot stand. See In re Warner, 379 F.2d 1011, 1017 (CCPA 1967). Accordingly, we do not sustain the rejection of claims 57 and 72, or of their dependent claims 58---62, 65-71, 73-75, and 102, as being unpatentable over Brown, Barbut, and Kreuzer. Rejection III Claims 63 and 64 depend from claim 57. Appeal Br. 28. The Examiner does not rely on Martin in any manner that would remedy the deficiency noted above with respect to claim 57. Therefore, for the same reasons as explained above, we do not sustain the rejection of claims 63 and 64 as being unpatentable over Brown, Barbut, Kreuzer, and Martin. Rejection IV The Examiner finds that Brown discloses a method as substantially recited in independent claim 92, including, inter alia, collecting a plurality of blood samples from a plurality of locations along the length of a catheter, the catheter having a sampling part and a reference guide sleeve, but does not "explicitly disclose that the catheter is flexible so as to be channeled through the blood vessel and has a blunt distal end." Final Act. 3-5, 10 (incorporating the findings and determinations made with respect to Rejection II). The Examiner finds that Kreuzer "teaches a catheter for sampling blood from a blood vessel wherein the catheter is flexible so as to be channeled through the blood vessel and has a blunt distal end," and reasons that it would have been obvious to modify Brown's device to have these features "to allow the catheter to be channeled into the blood vessel 8 Appeal2017-006668 Application 11/920,632 and avoid puncturing the vessel unnecessarily." Id. at 5---6. The Examiner finds that the combination of references as applied in Rejection II does not specifically disclose the reference guide sleeve which receives the sampling part is inserted into the body first; or that the reference guide sleeve and the sampling part have one or more indexing parts with respect to each other, which positions the sampling part at a predetermined position relative to the reference guide. Id. at 10. The Examiner relies on Sutton to teach these features. Id. at 10-11. Appellants traverse the rejection of claim 92 by incorporating arguments made with respect to claim 57 and by asserting that Sutton does not cure the deficiencies alleged in such arguments. Appeal Br. 24--25. We note that some of the arguments made with respect to claim 57-including the argument relied upon above regarding Rejection II-are not applicable because claim 92 does not include the relevant recitations. First, Appellants argue that Brown is non-analogous and, therefore, cannot properly be used in an obviousness rejection. Id. at 8-15. Appellants cite extensively to the Declaration of Dr. Stephen Blatcher ("Blatcher Deel."), one of the inventors. Id. A reference qualifies as prior art for a determination under § 103 when it is analogous to the claimed invention. In re Clay, 966 F.2d 656, 658 (Fed. Cir. 1992). Two separate tests define the scope of analogous prior art: (1) whether the art is from the same field of endeavor, regardless of the problem addressed, and (2) if the reference is not within the field of the inventor's endeavor, whether the reference still is reasonably pertinent to the particular problem with which the inventor is involved. 9 Appeal2017-006668 Application 11/920,632 In re Bigio, 381 F.3d 1320, 1325 (Fed. Cir. 2004) (citing In re Deminski, 796 F.2d 436,442 (Fed. Cir. 1986)). The field of endeavor is determined "by reference to explanations of the invention's subject matter in the patent application, including the embodiments, function, and structure of the claimed invention." Id.; see also Deminski, 796 F.2d at 442 (finding that if a prior art reference discloses essentially the same structure and function as the invention, it is likely in the same field of endeavor). Appellants argue that Brown is from a different field of endeavor because "[t ]he claimed invention is directed to collecting blood samples," and "Brown is directed to collection of tissue biopsies." Appeal Br. 9; see also Blatcher Deel. ,r,r 5-8. Appellants argue that Brown's device "includes a sharp tip 52 ... [that] is completely unsuitable for the claimed invention, which is channeled through a blood vessel for sampling the blood." Appeal Br. 9 ( citing Brown, 7: 1 O); see also Blatcher Deel. ,r,r 9-12. Appellants argue that "the device in Brown allows for portions that 'deliberately break off during use', which is completely incompatible with being located in a blood vessel." Appeal Br. 9 ( citing Brown, 8: 14--19); see also Blatcher Deel. ,r 12. Appellants argue that "Brown discloses a preferred sampling volume of less than 1.2 cubic millimeters," which "is far too small for the types of diagnostic chemistry analysis facilitated by the present invention." Appeal Br. 10 (citing Brown, 2:13, 5:26-27); see also Blatcher Deel. ,r 14. Appellants reproduce several portions of the Blatcher Declaration. Appeal Br. 10-13. We are not persuaded by Appellants' arguments, which mischaracterize Brown's catheter. Contrary to Appellants' assertion that Brown is "directed to collection of tissue biopsies" (id. at 9; see also 10 Appeal2017-006668 Application 11/920,632 Blatcher Deel. ,r 8), Brown repeatedly discloses collection of fluid samples. For example, Brown discloses that the internal vacuum of its vacuum sampling device embodiment "draws either tissue or fluid from the exterior of the chamber 3 into the chamber 3." Brown, 9: 15-16 ( emphasis added); see also id. at 12: 19-21 ("mechanisms for collecting samples of tissue or fluids" ( emphasis added)), 13: 5 ( contrasting biopsy and sampling). Contrary to the assertions of Appellants' declarant (see Blatcher Deel. ,r 9), this embodiment does not "need" material to be cut or include a blade; rather, Brown discloses that the covering material can be contoured to cut through material drawn into the cavity (Brown, 9 :24--26), which would be unnecessary for collecting fluid samples, and the referenced blade pertains to "[a]n additional embodiment" (id. at 9:31). Brown also refers to its device as "a biopsy and/or fluid sampling device." Id. at 1 :30 (emphasis added). Thus, like Appellants' device, Brown discloses a catheter for collecting fluid samples. Regarding the "sharp tip 52" cited by Appellants, Brown discloses: "The catheter 50 includes a distal insertion end 52 and sampling devices 54. The distal end 52 is a sharp or pointed end that is inserted into the subject requiring removal of tissue or fluid samples." Id. at 7:9-11. That Brown uses a sharp or pointed tip does not differentiate Brown's field of endeavor from that of Appellants' claimed invention. Rather, like Appellants' device, Brown discloses a medical catheter for insertion into a patient for biopsy or other purposes. See id. at 7: 8-9. Regarding Appellants' assertion that Brown allows for portions to deliberately break off, Brown discloses that its sampling devices are fabricated with biodegradable polymers, and that the use of such polymers 11 Appeal2017-006668 Application 11/920,632 "allows implementations of this invention with portions that deliberately break off during use, are left within the body, and cause no harm." Brown, 8:14--16. Continuing, Brown discloses that "[t]he sampling devices 54 need not be fabricated with biodegradable materials; however, use of biodegradable materials removes the danger associated with portions that break or fail during use." Id. at 8: 17-19. Thus, Brown contemplates implementations of its device that have portions that deliberately break off, but does not require such implementations as suggested by Appellants. A skilled artisan would not use such a frangible implementation where it would be undesired or dangerous to the patient. See KSR Int 'l Co. v. Teleflex Inc., 550 U.S. 398,421 (2007) ("A person of ordinary skill is also a person of ordinary creativity, not an automaton."). Regarding the volume of Brown's sampling chambers, Appellants focus on the preferred volume to the exclusion of Brown's full disclosure. As correctly noted by the Examiner (see Final Act. 7-8, 14; Ans. 23-24), Brown discloses that "[ v ]olumes of such sampling chambers range from as small as about a picoliter or less and as large as about a few hundred microliters [(µl)] or more." Brown, 10:5---6. Thus, Brown discloses a volume ranging from 1x10-12 liter to at least 1x10-4 liter, which encompasses the volume range recited by Appellants. The additional assertions made by Appellants' declarant similarly fail to persuade us that Brown is not analogous to the claimed invention. For example, the declarant' s characterizations of Brown's catheter as being "stiff' and "inflexible" (see Blatcher Deel. ,r,r 10, 12) are unsupported by evidence or persuasive technical reasoning, and the Examiner does not suggest reusing Brown's catheter (see id. ,r 13). We additionally note that 12 Appeal2017-006668 Application 11/920,632 Dr. Blatcher is also an Inventor/ Appellant and, as such, the Declaration is less persuasive than that of a disinterested person. See In re McKenna, 203 F.2d 717, 720 (CCPA 1953) ("[A]n affidavit by an applicant or co-applicant as to the advantages of his invention is less persuasive than one made by a disinterested person."). In view of the foregoing, we determine that a preponderance of the evidence supports the Examiner's determination that Brown is analogous to the claimed invention. See Ans. 15-16. Because both Appellants' method and Brown's device are directed to medical catheters for insertion into a patient for obtaining fluid samples, Brown is in the same field of endeavor as the claimed subject matter. Appellants next argue that Brown does not disclose obtaining a plurality of blood samples. Appeal Br. 15-16; see also Reply Br. 12-14. According to Appellants, "Brown is directed to removing solid tissue or fluid using 'scrapping or cutting using a jaw or knife mechanism,"' and "[t]he use of sharp or cutting edges is completely unsuitable for the claimed invention." Appeal Br. 15 (citing Brown, 3:5---6). We are not persuaded by Appellants' arguments. As noted above, Brown discloses a vacuum sampling device embodiment that draws fluid into its chambers and that does not use a jaw or knife mechanism. Additionally, as correctly noted by the Examiner (see Final Act. 3--4; Ans. 20), Brown discloses that "[t]he multiple sampling devices are positioned along the outer diameter of the shaft portion of a single catheter or other device, and samples are collected and stored in respective chambers of the sampling devices." Brown, 1:33-2:2; see also id. at Fig. 1. 13 Appeal2017-006668 Application 11/920,632 Finally, Appellants argue that "there is no disclosure in Brown of the need or desire to collect blood samples" and "[Kreuzer] contains no disclosure or teaching regarding sampling of any kind." Appeal Br. 19. According to Appellants, "one of ordinary skill in the art would not have been motivated by the disclosure of Kreuzer to modify the catheter of Brown to be flexible for intravascular use." Id. Continuing, Appellants argue that because "[t]he catheter of Brown was suitable for its purpose (e.g., collecting fluid samples from diseased areas) ... there would have been no reason for one of ordinary skill in the art to modify the catheter of Brown to collect blood samples." Id. Appellants argue that "neither Kreuzer nor Brown disclose how to use the microminature manufacturing technologies (Brown at p. 1) to make a catheter having the necessary dimensions to be inserted into a blood vessel." Id. ( citing Blatcher Deel. ,r 12). We are not persuaded by Appellants' arguments. As correctly noted by the Examiner, and as discussed above, Brown discloses the collection of fluid samples from a patient. Appellants fail to apprise us of error in the Examiner's determination that blood qualifies as such a fluid. See, e.g., Final Act. 13-14. For the same reasons, Appellants' arguments against the application of Kreuzer's teaching to Brown's device are unpersuasive. Given that Brown contemplates collecting samples of body fluid, such as blood, Appellant fails to apprise us of error in the Examiner's determination that a skilled artisan would have formed Brown's device of a flexible material and provided a blunt distal end as taught by Kreuzer. Regarding Appellants' arguments regarding the manufacturing of Brown's modified device, Brown does not require any specific manufacturing method. The assertion that Brown's device would require 14 Appeal2017-006668 Application 11/920,632 "significant re-engineering" is premised on Dr. Blatcher' s characterization of the Brown catheter as being inflexible. Appeal Br. 19-20 ( citing Blatcher Dec. ,r,r 12-13). However, as noted above, the declarant does not provide an evidentiary basis for this conclusory assertion. Moreover, as flexible vascular catheters are well known, as evidenced, for example, by Kreuzer, Appellants fail to persuade us that forming Brown's device of a flexible material would be beyond the skill set of a person of ordinary skill in the art. Accordingly, for the foregoing reasons, we sustain the rejection of claims 92-96 and 101 as being unpatentable over Brown, Barbut, Kreuzer, and Sutton. DECISION The Examiner's decision to reject claims 101 and 102 as being indefinite is reversed. The Examiner's decision to reject claims 57----62, 65-75, and 102 as being unpatentable over Brown, Barbut, and Kreuzer is reversed. The Examiner's decision to reject claims 63 and 64 as being unpatentable over Brown, Barbut, Kreuzer, and Martin is reversed. The Examiner's decision to reject claims 92-96 and 101 as being unpatentable over Brown, Barbut, Kreuzer, and Sutton is affirmed. No time period for taking any subsequent action in connection with this appeal may be extended under 37 C.F.R. § 1.136(a)(l )(iv). AFFIRMED-IN-PART 15 Copy with citationCopy as parenthetical citation