`__________
`
`BEFORE THE PATENT TRIAL AND APPEAL BOARD
`__________
`
`
`Moderna Therapeutics, Inc.
`
`Petitioner
`
`v.
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`Protiva Biotherapeutics, Inc.
`
`Patent Owner
`___________
`
`
`Case No. IPR2018-00739
`U.S. Patent No. 9,364,435
`
`___________
`
`
`PETITIONER’S SUR-REPLY TO PATENT OWNER’S
`CONTINGENT MOTION TO AMEND
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`
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`Mail Stop: PATENT BOARD
`Patent Trial and Appeal Board
`U.S. Patent & Trademark Office
`P.O. Box 1450
`Alexandria, VA 22313-1450
`
`10679120
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`Case No. IPR2018-00739
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`TABLE OF CONTENTS
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`I.
`II.
`
`Page
`INTRODUCTION ........................................................................................ 1
`DISCUSSION ............................................................................................... 1
`A. Patent Owner Fails To Rebut Petitioner’s Showing That The
`Substitute Claims Are Invalid ............................................................... 2
`B. Patent Owner Fails To Rebut Petitioner’s Showing that The
`Prior Art Discloses Systemic Use ......................................................... 6
`C. Patent Owner Fails To Rebut Petitioner’s Showing That
`Narrowed Claimed Concentrations Are Obvious ................................. 8
`D. Patent Owner Fails To Rebut Petitioner’s Showing That The
`Proposed Substitute Claims Lack Support And Are Not
`Enabled ............................................................................................... 11
`III. CONCLUSION ........................................................................................... 12
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`TABLE OF AUTHORITIES
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` Page(s)
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`Cases
`In re Baxter-Travenol Labs.,
`952 F.2d 388 (Fed. Cir. 1991) .............................................................................. 9
`In re Clemens,
`622 F.2d 1029 (C.C.P.A. 1980) ............................................................................ 8
`E.I. du Pont de Nemours & Co. v. Synvina C.V.,
`904 F.3d 996 (Fed. Cir. 2018) .............................................................................. 8
`Gemtron Corp. v. Saint-Gobain Corp.,
`572 F.3d 1371 (Fed. Cir. 2009) ...................................................................passim
`In re Peterson,
`315 F.3d 1325 (Fed. Cir. 2003) .......................................................................... 11
`Scentair Techs., Inc. v. Prolitec, Inc.,
`IPR2013-00179, Paper 84, 13 (P.T.A.B. Apr. 10, 2019) ..................................... 2
`Regulations
`37 C.F.R. § 42.6 ....................................................................................................... 10
`37 C.F.R. § 42.121 ................................................................................................... 11
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`LIST OF EXHIBITS RELIED UPON IN THE REPLY AND THE OPPOSITION TO AMEND
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`
`References
`
`U.S. Patent No. 9,364,435
`International Publication No. WO 2005/007196
`U.S. Publication No. US2006/0134189
`U.S. Publication No. US2006/0240554
`Lin, Alison J. et al., Three-Dimensional Imaging of Lipid Gene-
`Carriers: Membrane Charge Density Controls Universal
`Transfection Behavior in Lamellar Cationic Liposome-DNA
`Complexes, 84 BIOPHYSICAL JOURNAL, 3307–16 (2003) (“Lin”)
`Ahmad, Ayesha et al., New multivalent cationic lipids reveal bell
`curve for transfection efficiency versus membrane charge density:
`lipid-DNA complexes for gene delivery, 7 J GENE MED 739–48
`(2005) (“Ahmad”)
`Declaration of Dr. Andrew S. Janoff
`Gao, Xiang et al., Nonviral Gene Delivery: What We Know and
`What Is Next, 9 AAPS JOURNAL Article 9, pp. E92-E104 ( 2007)
`(“Gao”)
`Bennett, Michael J. et al., Cholesterol Enhances Cationic Liposome-
`Mediated DNA Transfection of Human Respiratory Epithelial Cells,
`15 Bioscience Reports, pp. 47-53 (1995) (“Bennett”)
`Heyes, James et al., Cationic lipid saturation influences
`intracellular delivery of encapsulated nucleic acids, 107 JOURNAL
`OF CONTROLLED RELEASE 276–87 (2005) (“Heyes”)
`U.S. Patent No. 5,753,613
`U.S. Patent No. 7,939,505
`U.S. Publication No. US2007/0042031
`U.S. Publication No. US2006/0008910
`Excerpts from ’069 Patent File History
`’435 Patent File History
`U.S. Patent No. 5,264,618
`Curriculum Vitae of Dr. Andrew S. Janoff
`Deposition Transcript of David H. Thompson – Volume 1 (February
`4, 2019)
`Deposition Transcript of David H. Thompson – Volume 2 (February
`5, 2019)
`
`iii
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`Exhibit
`No.
`1001
`1002
`1003
`1004
`1005
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`1006
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`1007
`1008
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`1009
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`1010
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`1011
`1012
`1013
`1014
`1015
`1016
`1017
`1018
`1019
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`1020
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`Exhibit
`No.
`1021
`1022
`1023
`1024
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`1025
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`1026
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`
`
`References
`
`Reply Declaration of Dr. Andrew S. Janoff
`Janoff Declaration for Opposition to Motion to Amend
`Patent Owner Response in IPR2018-00739
`Kauffman, et al. Optimization of Lipid Nanoparticle Formulations
`for mRNA Delivery in Vivo with Fractional Factorial and Definitive
`Screening Designs, Nano Letters (2015) (“Kauffman”)
`Decision on Appeal, Appeal No. 2016-008388 (P.T.A.B. July 18,
`2018)
`Transcript of April 30, 2019 Conference Call
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`I.
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`INTRODUCTION
`Patent Owner’s (“PO”) Reply in support of its MTA is nothing more than
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`attorney argument and mischaracterizations of the existing record, applicable rules,
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`and newly added references. It is well established that such attorney argument is
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`not evidence. Gemtron Corp. v. Saint-Gobain Corp., 572 F.3d 1371, 1380 (Fed.
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`Cir. 2009) (“[U]nsworn attorney argument ... is not evidence and cannot rebut ...
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`other admitted evidence ....”). Based upon the actual evidence of record, substitute
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`claim 21 presented in the MTA fails to remedy the issues raised in these
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`proceedings and is invalid by the preponderance of the evidence. Moreover, PO
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`fails to even address a prior Board decision addressing the failure of PO’s own
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`substantively similar disclosure to adequately describe use of mRNA payloads.
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`The Board’s reasoning in this prior decision is sound and equally applicable here.
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`II. DISCUSSION
`In its Opposition, Petitioner set forth its position that the “substitute claims …
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`do not remedy the invalidity issues raised” in the IPR proceeding. See Opp., 1.
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`Petitioner then went on to explain how each of PO’s added limitations (and the
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`substitute claim as a whole) are disclosed in the prior art. Id., 3-8.
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`Unable to substantively rebut Petitioner’s invalidity showing, PO resorts to
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`mischaracterizations of the record and applicable rules. For example, PO claims that
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`it cannot fathom the prior art combinations that underlie the discussions. Reply, 1.
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`Immediately thereafter, however, PO sets forth its response to the prior art
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`combinations of Grounds 1-3 as enumerated in the Petition. Id., 2-4. PO also
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`complains that the Opposition focuses on new limitations in the substitute claim and
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`does not reargue limitations that have remained substantively the same. See Reply,
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`2. There is no rule requiring rehashing of every argument in every filing. PO itself
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`cites to arguments put forth in its PO Response instead of needlessly repeating them
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`in this briefing. See, e.g., Reply, 2 (“Patent Owner believes that the addition of
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`‘serum stable’ is superfluous … (see Response 11-13) ….”). Indeed, PO’s own cited
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`case support states that “the Board determines whether substitute claims are
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`unpatentable by a preponderance of the evidence based on the entirety of the record
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`….” Scentair Techs., Inc. v. Prolitec, Inc., No. IPR2013-00179, Paper 84, 13-14
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`(P.T.A.B. Apr. 10, 2019) (emphasis added). While the panel in Scentair did reject a
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`generic reference in an Opposition to a MTA to un-instituted grounds in a Petition
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`regarding “one or more … ‘other’ references” presented regarding different claims
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`(id., 20), that is simply not analogous to the briefing here.
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`A.
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`PATENT OWNER FAILS TO REBUT PETITIONER’S SHOWING THAT
`THE SUBSTITUTE CLAIMS ARE INVALID
`The references of record establish that (1) certain cationic lipids (e.g., DLin-
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`DMA) are sufficiently non-toxic that they can be tolerated at high concentrations in
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`vivo and (2) nucleic acid-lipid particles with high cationic lipid concentrations (e.g.,
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`at or above 50 mol%) can be formed that are “substantially non-toxic” with such
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`lipids. See, e.g., EX1003, [0152] (cationic lipid 2-60 mol%), [0151] (resulting
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`particles “substantially non-toxic”); EX1022, ¶¶54-57 (sworn expert testimony on
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`substantially non-toxic ionizable cationic lipids). Rather than addressing the
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`substance of the prior art disclosures and related sworn expert testimony, PO resorts
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`to blatant mischaracterizations. See, e.g., Reply, 4 (calling disclosures “attorney
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`argument [and] a false narrative”). But the same basic science underlies the ’435
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`patent as well. EX1001, 3:18-20 (using DLin-DMA to create “… lipid particles
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`[that] are substantially non-toxic” at cationic lipid concentrations greater than 50
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`mol%). The question is whether this basic science was known prior to the ’435
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`patent, and the record indisputably demonstrates that this was in fact known.
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`PO also argues that all cationic lipids are toxic to some extent. Reply, 5. Even
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`if accepted as true, ionizable cationic lipids like DLin-DMA on the “lower end of
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`the toxicity spectrum” were admittedly known and used. EX1020, 268:12-15. Patent
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`Owner’s prior disclosures specifically state that “substantially non-toxic” nucleic
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`acid-lipid particles can be created using DLin-DMA in ranges up to 60 mol%.
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`EX1002, [0011], [0088]; EX1003, [0152], [0155]. The ’435 patent is based upon
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`almost verbatim disclosures but with the cationic lipid range adjusted slightly. See
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`EX1001, 3:13-31, 6:2-5 (“substantially non-toxic” particles using DLin-DMA). This
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`is in no way a “false narrative” as PO claims.
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`PO’s attempt to limit its prior disclosures of the cationic lipid range in
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`particles for systemic use to just 5-15 mol% (Reply, 3) is inconsistent with the other
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`disclosures therein. For example, the ’189 publication describes systematic in vivo
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`testing of 40 mol% cationic lipid. EX1003, [0351]-[0391] (2:40 formulation).
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`Limiting the cationic lipid range to 5-15 mol% for systemic use cannot be reconciled
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`with this systemic testing at 40 mol%—a fact PO and its expert conveniently ignore.
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`Unrelated new exhibits (EX2051-EX2052) do not change this analysis. First,
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`PO offers only unsupported attorney argument regarding these exhibits—this is not
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`evidence. Gemtron, 572 F.3d at 1380. Second, these references disclose work done
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`by Petitioner in 2016-2017 to further improve on ionizable cationic lipids. See
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`EX2051-2052. PO cherry picks single paragraphs from each of these references and
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`argues that these excerpts confirm that ionizable cationic lipids (e.g., DLin-DMA)
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`are too toxic to be used at high mol%. See Reply, 5. PO’s proposed conclusion,
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`however, directly contradicts not only the basic science underlying the ’189
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`publication, but the ’435 patent as well.
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`EX2051 is a 50-page disclosure detailing a “method for producing lipid
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`nanoparticles” using a “lower alkanol solution.” EX2051, 1:21-25. PO cites to a
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`single paragraph directed to a single embodiment regarding the optional use of
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`“biodegradable cationic lipids to produce … rapidly eliminated lipid nanoparticle
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`(reLNP).” Id., 21:9-18. The disclosure notes that such reLNPs can increase
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`tolerability because “[i]onizable cationic lipids, such as … DLinDMA … have been
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`shown to accumulate in plasma and tissues over time and may be a potential source
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`of toxicity.” Id. PO ignores that EX2051 discloses various high cationic lipid
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`embodiments (e.g., id., 9:23-26 (70 mol%)) and nowhere says that only
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`biodegradable cationic lipids should be used with such embodiments.
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`EX2052 is a 326-page disclosure detailing nucleic acid-lipid particles having
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`an improved structure comprising an “inner core” and “outer shell.” See, e.g.,
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`EX2052, cl. 1. PO again cites to a single paragraph stating that “the lipid compounds
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`described herein have a lower immunogenicity as compared to a reference lipid (e.g.,
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`MC3, KC2, or DLinDMA).” Reply, 5 (citing EX2052, 57:29-58:9). Again, the
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`reference in no way states that the reference lipids (e.g., DLin-DMA) are too toxic
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`to be used at high cationic lipid concentrations.
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`PO’s attorney’s argument that toxicity is unrelated to charge or whether a
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`cationic lipid is ionizable citing Ahmad (Reply, 5) is no more availing. Ahmad
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`discloses that “[m]embrane charge density is a universal parameter” (EX1006, 743)
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`and shows that at high membrane charge densities, transfection efficiency drops off
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`precipitously (id., Fig. 3). This is consistent with other cited prior art emphasizing
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`the importance of particle charge. EX1002, [0015] (overall neutral charge are
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`preferred), EX1003, [0219] (same); EX1010, 277 (“low surface charge required for
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`systemic delivery”). While Ahmad advocates the use of multivalent lipids, nowhere
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`does it state that toxicity is unrelated to charge. Even PO’s own expert admitted
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`charge may effect toxicity: “Q. … does the charge of the cationic lipid used, the pH
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`of the in vitro experiment affect its acute toxicity? A. The details matter. I can't—I
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`can't answer that with—with any kind of precision because it's—it depends on the
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`material and the formulation.” EX1019, 66:18-23.
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`B.
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`PATENT OWNER FAILS TO REBUT PETITIONER’S SHOWING THAT
`THE PRIOR ART DISCLOSES SYSTEMIC USE
`PO’s stated purpose for the added limitations regarding “serum stability and
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`nuclease resistance” is to limit “the claimed particles to those that are suitable for
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`systemic use.” Reply, 3. Each of the primary prior art references, however, disclose
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`both of these added limitations and systemic use. See, e.g., EX1002, [0002] (“serum-
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`stable nucleic acid-lipid particle”), cl.2, [0011] (“… the nucleic acid in the nucleic
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`acid-lipid particle is resistant in aqueous solution to degradation by a nuclease”),
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`[0204] (stability tested at 37 degrees for 30 minutes); EX1003, [0182] (“serum-
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`stable nucleic acid-lipid particles”), cl. 31 (“… the nucleic acid in said nucleic acid-
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`lipid particle is not substantially degraded after exposure of said particle to a
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`nuclease at 37° C. for 20 minutes.”), [0013] (nuclease resistance for “at least 20, 30,
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`45, or 60 minutes” at 37°C); EX1004, [0136] (“the present invention provides a
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`serum-stable formulated molecular composition ... in which the biologically active
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`molecule is encapsulated in a lipid bilayer and is protected from degradation”); see
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`also EX1022, ¶¶54, 60. Contrary to PO’s assertions (Reply, 6), these disclosures are
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`not limited to mere testing for nuclease degradation.
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`PO offers no substantive argument regarding these disclosures in the ’196
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`PCT and ’189 publication, arguing only that the provided disclosures are insufficient
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`without further explanation. See Reply, 6. It is unclear what more is required than
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`repeated disclosure of verbatim limitations in the prior art.
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`Regarding the ’544 publication, PO offers attorney argument that the
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`formulations disclosed therein are limited to the use of chemically modified RNA
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`constructs to protect the nucleic acid from enzymatic degradation. Reply, 4, 6. But,
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`that is only one of the disclosed embodiments. The ’544 publication also discloses
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`embodiments achieving nuclease resistance through encapsulation: “… serum-stable
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`formulated molecular composition (e.g., comprising a biologically active molecules
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`… including siNA …) in which the biologically active molecule is encapsulated in
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`a lipid bilayer and is protected from degradation ….” EX1004, [0136].
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`In any event, the substitute claim includes the term “serum-stable” only to the
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`preamble, which a POSITA would not consider limiting. See EX1022, ¶53. PO
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`nevertheless relies on the term to differentiate prior art. Reply, 2. PO offers no
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`evidence (e.g., sworn expert testimony) on importing this limitation from the
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`preamble, instead offering mere attorney argument that the term “is tied to the added
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`limitation” regarding nuclease degradation. Id., 3. PO also fails to address its own
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`expert’s testimony that the term “serum stable” has a different scope than the
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`nuclease degradation limitation. EX1020, 368:2-18 (nuclease degradation limitation
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`can refer to resistance to nuclease in vitro).
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`C.
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`PATENT OWNER FAILS TO REBUT PETITIONER’S SHOWING THAT
`NARROWED CLAIMED CONCENTRATIONS ARE OBVIOUS
`As presented in the Petition (Paper 2) and Reply (Paper 28), the overlapping
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`and encompassing ranges for the various lipid components in the prior art establish
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`a prima facie case of obviousness. E.I. du Pont de Nemours & Co. v. Synvina C.V.,
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`904 F.3d 996, 1006 (Fed. Cir. 2018) (“overlap [in ranges] creates a presumption of
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`obviousness”). By its motion, PO has proposed a narrowed range for the cationic
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`lipid to more closely align the claimed range with testing on which PO relies in an
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`attempt to demonstrate unexpected results to rebut this showing. See Reply, 8
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`(“The substitute claims narrow the cationic lipid range to 50% to 75% ....”). As
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`Petitioner has explained, the substitute lipid ranges, if anything, actually increase
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`the overlap with the prior art. See Opp., 8. PO’s complaint that the Opposition
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`focuses on the changes to the cationic lipid range (id., 7) makes no sense—of
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`course Petitioner is focused on PO’s substantive amendment. While PO also
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`increase the range for the non-cationic lipid accordingly to 23-49.5 mol% (MTA,
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`4), this amended range similarly increases the overlap with the prior art. EX1002,
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`[0091] (20-85%); EX1003 [0152] (20-80%); EX1004, [0313] (20-85%).
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`PO’s further efforts to rebut Petitioner’s showing are also insufficient. PO’s
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`test data is still not commensurate with the scope of the narrowed claims. In re
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`Clemens, 622 F.2d 1029, 1035 (C.C.P.A. 1980) (test data must be commensurate
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`with the scope of claims). First, the narrowed range for the cationic lipid
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`concentration is 50-75 mol%. Reply, 8. PO’s test data admittedly covers only
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`select points between the lesser range of 50-70 mol% and there is no basis to
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`believe that concentrations between 70-75 mol% would behave the same. MTA, 16
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`(test data in patent of “54 mol% to 70 mol%” and “post-filing date data” for “50
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`mol% and 57 mol% cationic lipid” (citing EX2017-19, EX2021)). To explain the
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`gap in the data, PO cites to a statement from the ’435 patent that “lipid ratios as
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`target formulations … may vary by ±5 mol%.” Reply, 8. But, as PO has pointed
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`out previously, the ’435 patent claim “recites a nucleic acid-lipid particle with
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`specific concentration ranges of” lipid components, not target formulations. POR,
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`39-40. Moreover, there is no evidence that the cited test formulations have cationic
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`lipid concentrations other than those stated.
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`Second, PO’s test data merely shows that the tested formulations, in some
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`cases, show some efficacy. See Reply, 8. It is well settled that “results must be shown
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`to be unexpected compared with the closest prior art.” In re Baxter-Travenol Labs.,
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`952 F.2d 388, 392 (Fed. Cir. 1991). During prosecution, PO compared the tested
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`formulations in the ’435 patent to the admitted prior art 2:40 formulation. EX1015
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`(PO argued Examples 3-4 show 1:57 formulation more effective than “previously
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`described (‘2:40 SNALP’)”). The testing beyond Examples 3-4 on which PO now
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`relies contains no basis for comparison to any prior art formulations. See EX1001
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`(Examples 2, 5-11); EX2017-19, EX2021, EX2047-50 (no comparison to prior art
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`formulations). This new “evidence” is thus irrelevant to the question of unexpected
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`results and does not impact the inquiry. In addition, PO’s post-’435 patent test data
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`demonstrates that certain formulations falling within the scope of the claims have no
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`activity whatsoever, let alone activity better than the prior art. Opp., 10 (discussing
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`examples). This shows that the data is not coextensive with the substitute claims.
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`Third, regarding new exhibits (EX2046-50), PO offers only unsupported
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`attorney argument—not evidence. Gemtron, 572 F.3d at 1380. Also, PO only makes
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`offhand reference to summary EX2046 without substantive discussion. Reply, 8.
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`This is improper under 37 C.F.R. § 42.6(a)(2).
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`Given the extensive overlap in the claimed ranges (e.g., 2-60 mol% in the
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`prior art compared to 50-75 mol% in the substitute claim) in a defined system
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`using the same lipid components, same formulation methods and same payloads
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`(see EX1001, EX1003), it would have been a matter of routine optimization for a
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`POSITA to select a cationic lipid concentration between 50-60% within the prior
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`art range. EX1007, ¶110 (“… determining the optimal proportion of cationic lipid
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`for a given lipid combination would be a simple matter of varying the proportion
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`using prior art methodologies.”). PO’s argument that motivation is lacking (Reply,
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`7-8) ignores the Federal Circuit’s holding that “[t]he normal desire of scientists …
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`provides the motivation to determine where in a disclosed set of percentage ranges
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`is the optimum combination of percentages.” In re Peterson, 315 F.3d 1325, 1330
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`(Fed. Cir. 2003).
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`D.
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`PATENT OWNER FAILS TO REBUT PETITIONER’S SHOWING THAT
`THE PROPOSED SUBSTITUTE CLAIMS LACK SUPPORT AND ARE NOT
`ENABLED
`Petitioner’s expert has offered testimony that a POSITA would not consider
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`the inventors of the ’435 patent to be in possession of nucleic-acid lipid particles
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`with an mRNA payload, and thus written description is lacking. EX1022, ¶68-77.
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`PO offers no rebuttal evidence (e.g., sworn expert testimony), but instead improperly
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`relies on mere attorney argument. Gemtron, 572 F.3d at 1380.
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`PO improperly points to disclosures regarding mRNA added to the ’435 patent
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`in 2015. The ’435 patent as filed contained claims referring only to generic “nucleic
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`acid” payloads (claim 1) or siRNA (claim 2). EX1016 (8/18/14 application). In 2015
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`(when PO was seeking to improperly expand the scope of its patent protections), PO
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`added the unsupported claim to mRNA (claim 2). Id. (2/26/15 Amendment). PO’s
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`reliance on this late-added claim for written description support is improper. 37
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`C.F.R. § 42.121(b)(2) (support required from “original disclosure”).
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`Regarding enablement, PO cites to testimony from its expert (Reply, 9) that
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`(1) conflicts with his prior repeated answers that a formulation for a given payload
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`is merely a “starting point for whatever nucleic acid [one] might want to deliver”
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`(EX1019, 109:23-111:17); and (2) PO’s attorneys only elicited on redirect and then
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`Case No. IPR2018-00739
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` U.S. Patent No. 9,364,435
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`only after meeting with the witness for 1 hour and forty minutes to specifically
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`discuss how he should answer redirect questions. EX1020, 413:7-16.
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`PO also offers attorney argument that mRNA has been shown to have some
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`effect with a formulation previously used with siRNA. Reply, 9 (citing to EX2019,
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`EX2048). These references are silent, however, on the additional research and
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`testing that was required. Indeed, EX2048 states that as of 2017, the authors “set out
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`to describe, for the first time, the pharmacology and toxicologic effects of repeated
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`administration of hEPO-mRNA in LNPs.” EX2048, 2. PO also points to testing
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`performed by Petitioner’s expert. Reply, 11. Dr. Janoff testified that after spending
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`3-4 months and $100K to try to make the system of the ’435 patent work with
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`mRNA, there was no functional system and extensive further testing would be
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`required. EX2055, 15:17-18:19; 87:11-88:18. This weighs against enablement.
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`Finally, PO offers no analysis whatsoever regarding the decision in Ex parte
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`Guild, in which the Board carefully analyzed substantively the same disclosures
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`regarding nucleic-acid lipid particle payloads in one of Patent Owner’s own prior
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`disclosures and determined there was a lack of support regarding mRNA. See
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`EX1025. The Board’s reasoning in Guild is firmly based in the applicable science
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`and the analysis is equally applicable to the present proceedings.
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`III. CONCLUSION
`For the foregoing reasons, Patent Owner’s motion to amend should be denied.
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`Dated: May 10, 2019
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`Respectfully submitted,
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`By: Michael R. Fleming
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`Michael R. Fleming (Reg. No. 67,933)
`C. Maclain Wells (Reg. No. 48,991)
`IRELL & MANELLA LLP
`1800 Avenue of the Stars, Suite 900
`Los Angeles, California 90067-4276
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`Attorneys for Petitioners
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`CERTIFICATE OF SERVICE
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`I hereby certify, pursuant to 37 C.F.R. section 42.6, that on May 10, 2019, a
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`complete copy of the PETITIONER’S SUR-REPLY TO PATENT OWNER’S
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`CONTINGENT MOTION TO AMEND is being served via electronic mail upon
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`the following:
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`WILSON SONSINI GOODRICH & ROSATI
`Michael T. Rosato, Reg. No. 52,182
`mrosato@wsgr.com
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`Steven W. Parmelee, Reg. No. 31,990
`sparmelee@wsgr.com
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`Sonja R. Gerrard, Reg. No. 72,802
`sgerrard@wsgr.com
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`Edward R. Reines
`Edward.reines@weil.com
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`Derek C. Walter
`Derek.walter@weil.com
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`Susan M. Langworthy
`Susan M. Langworthy
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