Ex Parte Anderson et alDownload PDFPatent Trial and Appeal BoardMar 12, 201913867510 (P.T.A.B. Mar. 12, 2019) Copy Citation UNITED STA TES p A TENT AND TRADEMARK OFFICE APPLICATION NO. FILING DATE 13/867,510 04/22/2013 93726 7590 03/14/2019 EPA - Bozicevic Field & Francis LLP Bozicevic, Field & Francis 201 REDWOOD SHORES PARKWAY SUITE 200 REDWOOD CITY, CA 94065 FIRST NAMED INVENTOR Carter R. Anderson 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. VERDE-001DIV2 7411 EXAMINER CHANNA V AJJALA, LAKSHMI SARADA ART UNIT PAPER NUMBER 1611 NOTIFICATION DATE DELIVERY MODE 03/14/2019 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): docket@bozpat.com PTOL-90A (Rev. 04/07) UNITED STATES PATENT AND TRADEMARK OFFICE BEFORE THE PATENT TRIAL AND APPEAL BOARD Ex parte CARTER R. ANDERSON and RUSSELL L. MORRIS 1 Appeal2018-000474 2 Application 13/867,510 Technology Center 1600 Before DEMETRA J. MILLS, TA WEN CHANG, and RACHEL H. TOWNSEND, Administrative Patent Judges. MILLS, Administrative Patent Judge. DECISION ON APPEAL This is an appeal under 35 U.S.C. § 134. The Examiner has rejected the claims 34--46 and 49-51 for obviousness. We have jurisdiction under 35 U.S.C. § 6(b). We reverse. 1 Appellants state that the real party in interest is Verde Environmental Technologies, Inc. App. Br. 3. 2 Related Appeals, Application No, 14/827 ,998, Appeal 2018-000621 and Application No. 14/828005, Appeal No. 2018-000874. Appeal2018-000474 Application 13/867,510 STATEMENT OF CASE The following claims are representative ( emphasis added). 34. A method for reducing potential for substance abuse from a skin-worn transdermal patch device comprising an abusable substance layer containing residual amounts of an abusable substance of interest after removal from a user, the method comprising: inserting the transdermal patch device into a container and thereby contacting the abusable substance layer of the transdermal patch device as removed from a user to an anti- abuse substance present in an anti-abuse layer that is attached to an interior wall of the container, wherein the anti-abuse substance is selected from the group consisting of co-soluble antagonists, irritants and combinations thereof so that the potential for abuse is reduced. 39. A system for reducing potential for substance abuse from a skin-worn transdermal patch device comprising an abusable substance layer containing residual amounts of abusable substance after administration to a user, said system compnsmg: (a) a disposable container having an opening therein to receive a skin-worn patch device containing a residual amount of an abusable substance therein; (b) an anti-abuse layer attached to an interior wall of the container and containing an amount of an anti-abuse substance selected from the group consisting of co-soluble antagonists, irritants and combinations thereof, said anti-abuse layer being disposed in said container in a manner such that a skin-worn patch device properly inserted into said container causes said abusable substance of said skin-worn patch device to contact said anti-abuse substance; and ( c) a closure for closing said container containing a used skin-worn patch device. 44. A method for reducing potential for substance abuse from a skin-worn transdermal patch device having an abusable 2 Appeal2018-000474 Application 13/867,510 substance layer containing a residual amount of an abusable substance of interest and an anti-abuse layer, the method compnsmg: contacting said abusable substance layer with said anti- abuse layer by removing the transdermal patch from a user and thereby removing a membrane from between the abusable substance layer and the anti-abuse layer, wherein said anti- abuse layer comprises a substance selected from the group consisting of co-soluble antagonists, irritants and combinations thereof. Cited References Warner et al. ("Warner") US 2005/0112068 Al May 26, 2005 Shevchuk et al. ("Shevchuck") US 2004/0126323 Al July 1, 2004 Cubbage et al. ("Cubbage") US 5,804,215 September 8, 1998 Grounds of Rejection 3-13. 1. Claims 34, 36-40, 42--43 are rejected under pre-AIA 35 U.S.C. § I03(a) as being unpatentable over Warner. 2. Claims 35 and 41 are rejected under pre-AIA 35 U.S.C. § I03(a) as being unpatentable over Warner further in view of Shevchuk. 3. Claims 44--46, 49, and 51 are rejected under pre-AIA 35 U.S.C. § I03(a) as being unpatentable over Cubbage in view of Warner. FINDINGS OF FACT The Examiner's findings of fact are set forth in the Answer at pages 3 Appeal2018-000474 Application 13/867,510 1. The system described by Warner includes a dermal patch containing an active substance such as fentanyl or other opiates (see ,r 36 and examples), which reads on the dependent claim limitations of instant claims 37-38 and 45--46, and further meets the claimed abusable substance. 2. According to Warner, the active agent (prone to unintended use), can be present in a first side of the dermal patch or peel and configured to deliver the active agent to skin or mucosa (i-f 10). In the method of reducing the unintended use of active agent, a destructive agent that is chemically reactive with the active ingredient is employed, which includes chemical substances such as sodium hypochlorite, oxidants, permanganate; trace metals, etc. (i-f 36 and ,r,r 42--43). 3. In Warner, the active agent can be chemically reacted with the destructive agent present in a supporting device or an absorber (i-fi-f 7-8). 4. Warner describes a device having a glue coated surface that is configured to adhere to the active containing adhesive side of the patch, such that the unspent active agent is rendered substantially inaccessible for unintended use (i-f 10). 5. Further, Warner describes that the device is configured to envelope and seal the dermal patch, such that the unspent active agent is rendered substantially inaccessible for unintended use (i-f 12). 6. In one embodiment, Warner teaches that a destructive material can be impregnated on to an absorber and stored in the container, 4 Appeal2018-000474 Application 13/867,510 wherein the container is provided with a resalable lid, cap, or plug to prevent spillage (i1i134--38). 7. Shevchuk teaches a tamper resistant dosage form comprising an active such as an opioid; an adverse agent such as an opioid antagonist and a salt thereof (abstract & figure 3A). 8. For the abusive drugs, Shevchuk teaches opioids (i158) including fentanyl and for the adverse agent, Shevchuk teaches opioid antagonists such as naloxone (i167). In particular, Shevchuk teaches combination of fentanyl and naltrexone (i1 78). 9. Shevchuk further teaches that in one embodiment, Fig 3A, wherein the active agent (opioid), and the adverse agent (antagonist), are separated by a barrier layer (i1 44). 10. Specification, Fig 1 is reproduced below. Specification, Fig. 1 shows, A disposal container or pouch designed to accompany the skin-worn patch 10 is shown generally by the reference character 16 and includes a layer of absorbent material 18 attached to one side of the container 16 in the manner such that insertion of the used skin-worn patch 10 as is shown by the arrow 20 with the opioid layer 14 facing the adsorptive material 18, ensures that contact will occur between the layers 14 and 18, thereby adsorbing and deactivating the 5 Appeal2018-000474 Application 13/867,510 opioid from layer 14. Spec. 7; italicized emphasis added. PRINCIPLES OF LAW In making our determination, we apply the preponderance of the evidence standard. See, e.g., Ethicon, Inc. v. Quigg, 849 F.2d 1422, 1427 (Fed. Cir. 1988) (explaining the general evidentiary standard for proceedings before the Office). "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'! Co. v. Teleflex Inc., 550 U.S. 398,416 (2007). Moreover, "obviousness requires a suggestion of all limitations in a claim." CFMT, Inc. v. Yieldup Int'! Corp., 349 F.3d 1333, 1342 (Fed. Cir. 2003) (citing In re Royka, 490 F.2d 981,985 (CCPA 1974)). Obviousness Rejections The Examiner finds that W amer "teaches a system drawn to and a method of reducing unintended use of an active ingredient, such as residual active ingredients present in spent dermal patches and peels ( abstract; 0007- 0014 ). " Final Act. 3. The Examiner finds that the: Instant claims do not require any glue coated anti-abuse layer and instead only require that the anti-abuse layer is attached to a side of the container. In other words, one of an ordinary skill in the art would be motivated to dispose the patch in to the glue-coated container with or without an absorber, and still be able to attach the spent patch (with residual active agent) to the glue coated surface of the disposing container. Ans. 12. 6 Appeal2018-000474 Application 13/867,510 Appellants contend that: the Examiner errs in asserting that the glue-coated surface and absorber are described in one embodiment. The system of paragraph [001 OJ fails to disclose any absorber element and the method of Claims 3 8 and 41 of Warner fails to disclose any glue-coated device. Nowhere does Warner teach or suggest that the glue-coated device and a container having an absorber are both components of a single embodiment. As reviewed above, Warner provides no guidance to a container where an anti-abuse layer is attached to an interior wall of a container. App. Br. 6; italicized emphasis added. ANALYSIS Rejection 1- Obviousness Warner We do not find that the Examiner has provided evidence to support a prima facie case of obviousness. The dispositive issue for each of the rejections is whether Warner teaches an "anti-abuse substance present in an anti-abuse layer that is attached to an interior wall of the container." Claim 34. Claim 34 requires, "in an anti-abuse layer that is attached to an interior wall of the container." (emphasis added). "[O]bviousness requires a suggestion of all limitations in a claim." CFMT, Inc. v. Yieldup Int 'l Corp., 349 F.3d 1333, 1342 (Fed. Cir. 2003) (citing In re Royka, 490 F.2d 981,985 (CCPA 1974)). The burden is on the examiner to set forth a prima facie case ofunpatentability. See In re Glaug, 283 F.3d 1335, 1338 (Fed. Cir. 2002). We agree with Appellants that "Warner provides no guidance to a container where an anti-abuse layer is attached to an interior wall of a 7 Appeal2018-000474 Application 13/867,510 container." App. Br. 6. The Examiner contends that the absorber, which may be included in a container, "implicit[ly] ... sticks to the interior of the container ... because a solution or an absorber material in a container touche[s] the bottom and/or side surfaces of the container." (Ans. 11.) The Examiner further states that "it would have been obvious for one of an ordinary skill in the art at the time of the instant invention was made to place the glue-coated absorber in a suitable position to the sides or the base of the container and see that the patch with unspent abusive agent is properly attached/secured to the absorber .... " (Id.) We do not agree with the Examiner that Warner teaches a glue-coated absorber or that the absorber is inherently "attached" to a container in Warner. In particular, Warner teaches separate embodiments, one that involves the use of a destructive agent that deactivates the active agent of a spent dermal drug delivery device (i1i1 7-9), and another that involves adhering the spent dermal drug delivery device to a glue coated surface of a device (i-fi-fl0-11). The Examiner has not indicated where the prior art discloses a container where an anti-abuse layer is attached to an interior wall of a container, as claimed. Rejections 2 and 3 as set forth in the Grounds of Rejection also rely on Warner for the claimed feature of a container where an anti-abuse layer is attached to an interior wall of a container. In addition, Cubbage, Fig. 2, discloses a transdermal patch disposal system where "the inner surface 21 of the preferred substrate 20 is coated with an adhesive 22 which is aggressively self-sticking such that once the facing surface 21 of the disposal substrate 20 is pressed against itself." Col. 2, 11. 64-68. However, the Examiner has not provided evidence in the prior art that either Warner or 8 Appeal2018-000474 Application 13/867,510 Cubbage disclose an "anti-abuse substance present in an anti-abuse layer that is attached to an interior wall of the container," as claimed. W amer discloses the inclusion of a destructive agent in a method for reducing the unintended use of active ingredients in dermal delivery devices i-f3 6, but does not specifically disclose that the anti-abuse substance/layer is attached to an interior wall of the container. Rejections 2-3 are reversed for the same reasons as rejection 1. CONCLUSION OF LAW The cited references do not support the Examiner's obviousness rejections, which are reversed. REVERSED 9 Copy with citationCopy as parenthetical citation