`Filed: Enter a date.
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`UNITED STATES PATENT AND TRADEMARK OFFICE
`____________________
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`BEFORE THE PATENT TRIAL AND APPEAL BOARD
`___________________
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`NEPTUNE GENERICS, LLC
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`PETITIONER
`
`V.
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`AVENTIS PHARMA S.A.
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`PATENT OWNER
`
`___________________
`
`CASE NO.: IP2019-00136
`PATENT NO. 5,847,170
`FILED: MARCH 26, 1996
`ISSUED: DECEMBER 8, 1998
`INVENTORS: HERVÉ BOUCHARD,
`JEAN-DOMINIQUE BOURZAT, ALAIN COMMERÇON
`
`
`TITLE: TAXOIDS, THEIR PREPARATION, AND PHARMACEUTICAL
`COMPOSITIONS CONTAINING THEM
`___________________
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`PETITIONER’S REQUEST FOR REHEARING
`UNDER 37 C.F.R. § 42.71(d)(1)
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`TABLE OF CONTENTS
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`I.
`Statement of Precise Relief Requested ....................................................................... 1
`II. Legal Standard for Rehearing ....................................................................................... 3
`III. Statement of Reasons for Relief Requested .............................................................. 4
`A. The Panel Erred in Determining Neptune’s Use of a Different Lead
`Compound Was Substantially Similar to Mylan’s Arguments ............................. 5
`B. The Panel Erred in Finding Commerçon and Neptune’s Related Arguments
`Are Cumulative to Arguments Presented in Mylan ............................................... 9
`C. The Decision Erred in Finding Wong and Klein Substantially Similar ....... 14
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`i
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`I.
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`STATEMENT OF PRECISE RELIEF REQUESTED
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`Petitioner Neptune Generics, LLC (“Neptune”), requests rehearing, pursuant
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`to 37 C.F.R. § 42.71(d)(1), of the Board’s Decision denying institution of review
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`for challenged claims 1-2 of U.S. Patent No. 5,847,170 (“the ’170 patent”). (Paper
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`15, “Decision” or “Dec.”). Petitioner is simultaneously requesting a Precedential
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`Opinion Panel by contacting the appropriate e-mail address, as instructed in the
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`relevant Standard Operating Procedure. The proper application of 325(d) to a new
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`chemical compound obviousness analysis is of such extraordinary and recurring
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`importance to the PTAB and its participants that a precedential panel is necessary
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`to supply uniform guidance for future cases. The panel denied institution because
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`the prior art or arguments in Neptune’s petition were purportedly “substantially
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`similar” to those presented in a previous petition in Mylan Laboratories Limited v.
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`Aventis Pharma S.A., IPR2016-00627 (filed Feb. 17, 2016). See Dec. at 25-35.
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`This finding distorts both 325(d) and the law of obviousness.
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`The panel found “substantial similarity” even though Neptune presented:
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`(1) a different lead compound (paclitaxel) and different reasons for selecting the
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`lead compound than Mylan’s lead compounds (Kant Compound 20 or docetaxel);
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`(2) a different primary reference for selection of paclitaxel as the lead compound
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`and for promising areas for substitutions of that lead compound (Commerçon) than
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`Mylan used to select and modify its different lead compounds (Kant); (3) different
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`1
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`primary references for substitution at the C-7 position (Commerçon and Wong)
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`than Mylan used for C-7 substitution (Klein); and (4) a different primary reference
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`for substitution at the C-10 position (Commerçon) than Mylan used (Kant), as well
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`as different arguments for applying Kant—the only Neptune primary reference
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`that overlaps with a Mylan primary reference—as an additional basis to substitute
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`paclitaxel’s C-10 position (Kant’s paclitaxel data as a control) than Mylan used
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`when it applied Kant as its sole reference to modify its different lead compound
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`(Kant contains no data as a control that supports modifying the C-7 position of
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`Compound 20 or docetaxel); and (5) a different expert declarant presenting a
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`different lead compound and different primary references.
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`Neptune respectfully submits that the panel overlooked or misapprehended
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`the law governing new chemical compound obviousness, the plain and material
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`factual differences between the art and arguments in the Neptune and Mylan
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`petitions, and misapprehended or misapplied recent 325(d) decisions to reach an
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`unreasonable judgment in weighing the relevant factors. Section 325(d) simply
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`does not (and cannot) support discretionary denial of an obviousness challenge to a
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`new chemical compound where the lead compound, and two of the three primary
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`references presented in support of modifying it—have never been presented to or
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`considered by the Patent Office—particularly where the Office rejected the prior
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`petition because the lead compounds selected had no evidentiary support and were
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`2
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`based entirely on hindsight. Neptune argued the challenged claims are obvious
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`when a POSA starts with paclitaxel, and modifies it based on Commerçon, Kant
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`and Wong. Mylan’s petition did not select paclitaxel as a lead compound—and it
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`did not even cite Commerçon or Wong. A discretionary denial under these
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`circumstances makes a mockery of both 325(d) and the law governing obviousness
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`of new chemical compounds.
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`For these reasons, as discussed in detail below, Neptune respectfully
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`requests rehearing of the panel’s decision declining to institute review.
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`II. LEGAL STANDARD FOR REHEARING
`A rehearing request “must specifically identify all matters the party believes
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`the Board misapprehended or overlooked, and the place where each matter was
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`previously addressed in a motion, an opposition, or a reply.” Id. Institution
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`decisions are reviewed on rehearing for an abuse of discretion. See 37 C.F.R. §
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`42.71(c). “An abuse of discretion may be indicated if a decision is based on an
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`erroneous interpretation of law, if a factual finding is not supported by substantial
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`evidence, or if the decision represents an unreasonable judgment in weighing
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`relevant factors.” Google LLC v. Cywee Group Ltd., IPR2018-01257, Paper No. 12
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`at 2 (Jan. 30, 2019) (citing Star Fruits S.N.C. v. U.S., 393 F. 3d 1277, 1281 (Fed.
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`Cir. 2005).
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`3
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`III. STATEMENT OF REASONS FOR RELIEF REQUESTED
`Neptune’s Petition established that a POSA starting with paclitaxel as the
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`lead compound renders the cabazitaxel of challenged claim 1 in view of the
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`Commerçon (Ex. 1009), Kant (Ex. 1010), and Wong references (Ex. 1011). (Pet. at
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`36-37.) Mylan’s prior petition selected Kant Compound 20 or docetaxel as lead
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`compound argued obviousness based on Kant and Klein. (Pet. at 77-78.) Neither
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`Neptune’s obviousness argument, nor Neptune’s combination of references has
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`ever been considered by the Office. (Pet. at 77-78; Reply at 1-4.) In fact, Neptune’s
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`lead reference, Commerçon—has never been presented to or considered by the
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`Office. (Pet. at 26, 77-78; Reply at 1.) And Neptune’s Wong reference has never
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`been considered by the Board, and although a European counterpart to Wong was
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`cited during prosecution, the Office has never commented on Wong or applied any
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`rejection based on Wong. (Pet. at 31, 77-78; Dec. at 19, n.4, and at 30, n.21.)
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`In denying institution, the panel overlooked or misapprehended both the law
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`of new chemical compound obviousness and the differences between Neptune’s
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`and Mylan’s petitions. Under black-letter law governing the obviousness analysis
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`for a new chemical compound, neither Neptune’s art, nor its arguments presented
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`in its Petition are similar—much less substantially similar—to the arguments
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`presented to and considered by the Board in Mylan’s petition.
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`4
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`A. The Panel Erred in Determining Neptune’s Use of a Different Lead
`Compound Was Substantially Similar to Mylan’s Arguments
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`In a challenge to a claim directed to a new chemical compound, the selection
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`of a lead compound is the “anchor” of any obviousness theory. Eisai Co. Ltd. v.
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`Dr. Reddy's Labs., Ltd, 533 F.3d 1353, 1359 (Fed. Cir. 2008). A lead compound is
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`“a compound in the prior art that would be most promising to modify in order to
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`improve upon its [] activity and obtain a compound with better activity.” (Pet. at
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`37, citing Takeda at 1357.) The analysis “focuses” on the identification of a lead
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`compound to determine whether “the skilled artisan would have had a reason to
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`select from the panoply of known compounds in the prior art.” Otsuka Pharm. Co.
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`v. Sandoz, Inc., 678 F.3d 1280, 1292 (Fed. Cir. 2012). (Pet. at 36, citing Otsuka.)
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`Mylan selected Kant Compound 20 and docetaxel as its lead compounds for
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`grounds one and two, respectively. (Pet. at 78.) The Board denied institution
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`because it found Mylan failed to present sufficient evidence showing a POSA
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`would select Compound 20 as a promising compound for further modification.
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`(Pet. at 77-78; Reply at 2, n.1.) Not a single one of the reasons the Board raised in
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`rejecting Compound 20 as the lead applies to paclitaxel as the lead compound (Pet.
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`at 2-3)—and nothing in the Decision found to the contrary. That should end the
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`inquiry under 325(d). (Pet. at 78); Juniper Networks, Inc. v. Finjan, Inc., IPR2019-
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`00026, Paper 7 at 25 (PTAB April 9, 2019) (instituting review, “[b]ecause [the
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`new reference] does not share those deficiencies [of previously presented
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`5
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`
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`reference], we find that Petitioner’s arguments concerning [new reference], also
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`differ substantively from those present by the previous petitions.).
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`First, the Mylan decision denying institution (“Mylan”) held that a POSA
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`would not select Compound 20 as the lead compound—a finding the Decision here
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`did not and could not make—which unmistakably establishes Neptune presented
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`different art and different arguments to the Board than Mylan’s petition:
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`Kant Compound 20 as a lead compound
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`We begin by observing that Kant uses 10-DAB as “the ideal
`starting material” to synthesize paclitaxel analogues by selective
`substitution at only the C-10 position. Ex. 1005, 5543 ¶ 3. Kant does not
`teach or suggest additional structural modifications to Compound 20 or
`docetaxel, which cuts against the notion of selecting Kant Compound 20
`as a lead compound for further modification of this docetaxel analogue.
`Kant itself indicates the authors chose to use 10-DAB as the starting
`material for making selective C-10 substitutions in order to synthesize
`“novel paclitaxel analogues.” Id. (Mylan at 12.)
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`Mylan found that starting with Compound 20 as the lead compound was not
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`supported by the sole reference (Kant) Mylan cited in support of selecting it. (Pet.
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`at 2, n.1.) And it is indisputable that Neptune identified paclitaxel as lead—which
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`is not subject to Mylan’s finding that Kant does not support selecting Compound
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`20 as the lead compound. To the contrary, Neptune uses Kant as a supporting
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`reference to modify lead compound paclitaxel—which Mylan expressly found
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`Kant to teach. (Reply at 2, n.1, citing Mylan, 10-11.) Paclitaxel is not only a
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`6
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`suitable lead compound, as was detailed in Neptune’s petition, it is the most
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`suitable lead compound, as Patent Owner admitted. (Pet. at 37-38.)
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`Mylan also rejected Compound 20 as the lead base on hindsight bias:
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`Petitioner also errs by starting with a hindsight-biased structural
`comparison of docetaxel, Kant Compound 20, and cabazitaxel in side-
`by-side fashion. Prelim. Resp. 31–34 (citing Pet. 31). As noted by Patent
`Owner, without a docetaxel control, Kant does not provide any
`information as to whether a particular compound performs better or
`worse than docetaxel. Id. at 33. Kant makes clear that the authors were
`synthesizing paclitaxel analogues and using paclitaxel, not docetaxel, as a
`control. Ex. 1005, 5545 Table II n.a (IC50 cytotoxicity measured as a “[r]atio
`of analogue relative to paclitaxel”). (Mylan at 12, cited in Reply at 2, n.1.)
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`Here again, Mylan’s criticism of using Kant to modify lead Compound 20
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`does not apply to Neptune’s Petition—because the lead compound is paclitaxel—
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`which is the very compound Kant used as a control in the context of synthesizing
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`paclitaxel analogues. (Pet. at 47-48.)
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`Mylan also rejected the argument that Kant suggested the possibility of
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`simultaneous substitutions of both the C-7 and C-10 positions of Compound B to
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`increase lipophilicity:
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`Kant also does not teach or suggest the possibility of simultaneous
`substitution of both the C-7 and C-10 positions, whether to increase
`potency and lipophilicity (cell membrane permeability) as argued by
`Petitioner (Pet. 21–22, 33), or for some other reason. Prelim. Resp. 20–26.
`Rather, Kant focuses on the possibility of improving anti-tumor cytotoxicity
`of paclitaxel analogues by selective substitution and functionalization of
`only the C-10 position, a point aptly made in the title, abstract, and text of
`Kant’s article… Petitioner does not address why a POSA would have
`simultaneously modified the C-7 and C-10 positions in Kant Compound
`20 to optimize lipophilicity, thereby minimizing aqueous solubility, when a
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`7
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`POSA would have known docetaxel and paclitaxel were highly
`lipophilic and insoluble in water, which made their commercial
`formulation challenging… Petitioner recognizes that alkylating the C-7 and
`C-10 functional groups would optimize lipophilicity (Pet. 22) but does not
`address the well-known problems with lipophilicity and limited aqueous
`solubility of intravenously administered paclitaxel and docetaxel.
`(Mylan at 13.)
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`In contrast, Neptune relied on Commerçon and laboratory best practices—
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`not Kant alone—to establish motivation and expected success for substitutions of
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`both the C-7 and C-10 positions. (Pet. at 39-40, citing Commerçon, best practices,
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`Dr. Wood; see also Reply at 4 (“nor does Neptune’s petition focus on a motivation
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`to increase lipophilicity…[which] separately addressed and accounted for
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`motivations regarding increased stability and any solubility concerns”).) Neptune
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`relied on Kant and Wong to establish an “additional motivation” (i.e., additional to
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`Commerçon) (Pet. at 40) for a POSA to make a substitution at the C-7 position—
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`which is exactly what Mylan found Kant to teach—and did so in the context of
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`modifications to paclitaxel (Neptune’s lead compound) not modifications to
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`Compound 20 (Mylan’s lead compound). Mylan at 13. Moreover, unlike Mylan’s
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`petition—Neptune did not argue that a POSA would be motivated to make
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`substitutions of the C-7 and C-10 positions to increase lipophilicity—an argument
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`Mylan appropriately rejected as shown above. Likewise, Neptune both
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`acknowledged and addressed the potential lipophilicity issue from the C-7 and C-
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`10 substitutions (Pet. at 46-50; Reply at 4)—but did not argue that increased
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`8
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`lipophilicity is a reason to make the substitutions. Both the art and arguments
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`Neptune presented on this issue are completely different than presented before.
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`Mylan also found a POSA would not modify Compound 20 based on the
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`teachings of Mylan’s second reference, Klein. Critically, Mylan found that the
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`petition failed to explain “why a POSA would have disregarded [a] key teachings
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`of Klein [to] increase aqueous solubility and chemical stability by reducing the C-9
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`carbonyl to a hydroxyl…in order to synthesize cabazitaxel from Kant Compound
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`20.” Mylan at 15.
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`This criticism simply does not apply to the art and arguments in Neptune’s
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`petition. Unlike the art and arguments in Mylan, Neptune did not select Compound
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`20 as the lead compound for modification—nor did it rely on the Klein reference
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`for modifications of its lead compound in its obviousness ground based on
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`Commerçon, Kant, and Wong. Juniper Networks, IPR2019-00026, Paper 7 at 25.
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`B.
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`The Panel Erred in Finding Commerçon and Neptune’s Related
`Arguments Are Cumulative to Arguments Presented in Mylan
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`Mylan’s petition does not identify or rely in any way on the Commerçon
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`reference (Ex. 1009), which Neptune relied upon as its lead reference for selecting
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`its lead compound and how to modify it. (Pet. at 78; Reply at 1.)1 “That the
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`principal reference asserted by Petitioner in this proceeding” was not previously
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`1 Mylan’s petition refers to a different Commerçon reference, (Mylan Ex. 1016),
`referred to as the Margraff reference in the Neptune petition (Ex. 1018).
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`9
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`“considered on the merits weighs against a discretionary denial when applied” to
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`the 325(d) factors. Garmin Intl. v. Wisc. Archery Prod., LLC, IPR2018-01137
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`(PTAB Dec. 11, 2018) (Paper 11 at 40).
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`Indeed, no better lead compound obviousness illustration could be presented
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`than in the prior art by Commerçon Fig. 2. (Pet. at 27, 37-42.) Titled
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`“Modifications influencing the cytotoxicity of paclitaxel” the figure succinctly
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`shows paclitaxel as a lead compound, shows portions of the molecule that are
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`“crucial” and must not be altered, shows a portion that is flexible at position 3’
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`(with a preference for the patent’s claimed BOC over paclitaxel’s PhCO), and
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`shows two flexible portions at positions C-7 and C-10. (Id.) The Decision simply
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`does not identify any reference cumulative to Commerçon—and its broad-brush
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`reliance on Mylan’s “background” as a substitute for Neptune’s lead reference is
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`clear error. Plain as could be, this lead compound is revealed along with a roadmap
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`for well-defined changes that would lead one directly to the claimed cabazitaxel, in
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`view of Kant and Wong. There is no such roadmap in Mylan’s petition, and thus
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`the two petitions are not cumulative or “substantially similar.”
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`The Decision misapprehended or overlooked Neptune’s scope of reliance
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`upon Commerçon when it adopted Patent Owner’s argument that Commerçon
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`merely disclosed that functional groups located at the C-7 and C-10 positions of an
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`analog were available for possible substitution. (Dec. at 31-32 citing POPR at 23-
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`10
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`24.) But Neptune relied on Commerçon to show much more, including: 1) the
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`phenylisoserine side-chain, as well as main carbon skeleton defined by C-1
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`through C-14, and most functional groups on the lower portion of the molecule are
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`all “crucial” to biological activity; 2) replacing the benzoyl with a BOC group at
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`C-3’in paclitaxel presented superior activity; (3) the C-7 and C-10 positions on the
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`main skeleton were flexible, able to withstand replacements without decreasing
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`activity; (4) the phenyl group directly attached at C-3’ was important and
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`significantly more active than methyl or hydrogen at that position, and that it is
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`most active in its unsubstituted rather than substituted form; and (5) per Figure 2,
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`Neptune argued Commerçon disclosed to a POSA that the vast supermajority of
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`locations in the paclitaxel analog, following the substitution of the benzoyl with a
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`BOC group at C-3', should be maintained, because they constituted either the most
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`active known functional groups at those locations, or those groups were crucial and
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`their removal would otherwise decrease an analog’s biological activity. (Pet. at 27-
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`29, 39, 40-42; Reply at 1.)
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`The Decision compounded its error when it did not even consider the alleged
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`cumulative nature of Commerçon on its own, but stated simply that all of
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`“Petitioner’s background discussion and reliance on Commerçon is, on balance
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`cumulative to art and arguments that the Board already considered in the Mylan
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`proceeding.” Dec. at 32. By painting with such an overly broad brush—and not
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`11
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`even addressing the totality of disclosures from Commerçon, and arguments
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`Neptune presented about Commerçon, the Decision committed clear error.
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`“A reference is cumulative when it teaches no more than what a reasonable
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`examiner would consider to be taught by the prior art already before the PTO.”
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`Regeneron Pharm., Inc. v. Merus N.V., 864 F.3d 1343, 1350 (Fed. Cir. 2017). The
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`Decision at 31-32 provides no basis to determine that many of the specific
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`disclosures within Commerçon identified by Neptune, and relied upon in
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`Neptune’s arguments (such as the motivation and basis for not changing the vast
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`majority of the disclosed paclitaxel analog, except at the C-7 through C-10
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`locations, such that these unchanged portions remain consistent with the claimed
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`cabazitaxel structure of the challenged claims) are cumulative with arguments in
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`Mylan’s Petition. (Pet. at 1, 3-5, 27-29, 39, 40-42, 56; Reply at 1.)
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`Likewise, Mylan and Neptune’s background sections reveal numerous
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`distinct, non-cumulative arguments presented. (Compare, e.g., Mylan’s reference
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`to the purported superiority of docetaxel over paclitaxel (Ex. 2011 at 20-21) which
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`was of course absent from Neptune’s background section (Pet. at 17-18); Mylan’s
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`affirmative motivation to increase a taxol analog’s lipophilicity (Ex. 2011 at 22)
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`versus Neptune’s absence of such an affirmation motivation, instead emphasizing a
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`motivation to maximize an analog’s biological activity before addressing solubility
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`issues, which could be significantly addressed through formulation studies (Pet. at
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`12
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`23-24; Reply at 3-4). Far from being cumulative, each petition’s background
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`section presented and emphasized issues more central to their respective different
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`lead compounds, and respective different primary references in support of
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`different steps taken by a POSA using different motivations to make different
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`modifications of their different lead compounds. Further Neptune presents an
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`extensive discussion of best laboratory practices involving detailed examples and
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`images of homologation and explanations regarding prodrugs (Pet. 20-22),
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`compared to Mylan’s lengthy discussion based on different motivations for
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`simultaneous substitution of functional groups at the C-7 and C-10 positions. (Ex.
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`2011 at 24-25). Accordingly, the Decision abused its § 325(d) discretion by
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`erroneously and unreasonably determining that key disclosures and arguments
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`Neptune made with respect to Commerçon (such as the motivation to maintain the
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`majority of the taxane analog that is consistent with the claimed cabazitaxel
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`structure) are cumulative of arguments made in by Mylan. Samsung Elec. Co., Ltd.
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`v. Immersion Corp., IPR2018-01469, Paper No. 10 at 13-14(PTAB March 7, 2019)
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`(rejecting 325(d) argument where it “is not merely the presence of an additional
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`reference but rather that the additional reference changes the character of the
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`overall teaching of the art to be something different from what the examiner
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`considered before.”) In view of the above, the Decision overlooked the way
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`Neptune’s arguments, particularly with respect to Commerçon and the process of
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`13
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`modifying paclitaxel, are “presented in a different manner with a different focus”
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`than Mylan’s failed petition. Becton Dickinson, IPR2017-01586, Paper 8 at 17–18.
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`C. The Decision Erred in Finding Wong and Klein Substantially Similar
`No reasonable examiner reviewing Klein and Wong would find these
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`references remotely similar—much less find that Wong “teaches no more” than
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`Klein. Klein discloses 9-dihydrotaxane analogs, which Mylan used in support of
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`modifications to Compound 20 (which is not a 9-dihydrotaxane)—and Wong
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`discloses paclitaxel analogs, which Neptune used in support of modifications to
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`paclitaxel. Thus, apart from the fact that Klein and Wong are clearly different
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`references directed to synthesizing different compounds—those different
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`references were used in support of making different modifications to different
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`lead compounds. There is no interpretation of 325(d) that can result in a finding
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`that these references are even a little bit similar—much less substantially similar.
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`See, e.g., Unified Patents Inc., v. Bradium Tech. LLC., IPR2018-00952, Paper 31
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`at 16 (PTAB December 20, 2018) (325(d) not triggered where a different petitioner
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`relied on combination involving one new and two old references).
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`In short, Mylan used Klein in error (as the Board found) in an attempt to
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`show motivation to make a substitution of Kant Compound 20 at the C-7
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`position. The Board found a POSA would not use Klein to modify Kant Compound
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`20 because it required ignoring a key teaching of Klein—a teaching that is not in
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`14
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`any of Neptune’s references Commerçon, Kant, or Wong. The Board found Mylan
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`could not use Klein in support of making a change to Compound 20 at C-7—while
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`rejecting Klein’s teaching about position C-9. Mylan at 16. Wong does not suffer
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`from this deficiency. Finding the references cumulative was legal error. This,
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`however, constitutes legal error. Regeneron, 864 F.3d at 1350; Juniper Networks,
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`IPR2019-00026, Paper 7 at 25; Amneal Pharma. v. Almirall, LLC, IPR2019-00207
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`at 115-117 (PTAB May 10, 2019) (Paper 8) (rejecting Patent Owner “swapped”
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`arguments amid improved or better disclosure). Although Neptune cited Klein, it
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`was for motivation to not alter the C-9 functional group in view of Commerçon,
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`Kant, or Wong disclosures. (Pet. at 44-45.) Unlike Mylan, Neptune did not rely
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`upon Klein as a primary reference. Neptune and Mylan used Klein for
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`fundamentally different purposes. See Vestas-American Wind Tech., Inc. v. Gen.
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`Elec. Co., IPR2018-01563 (reference that is found deficient or insufficient for
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`reading on a particular limitation can nonetheless still serve a different purpose).2
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`2 The Decision erred in finding that District Court litigation on appeal supports
`non-institution. First, this was not an independent reason to decline institution, and
`if the 325(d) analysis fails, rehearing is required. Second, Neptune’s obviousness
`combination was not presented, its references appear only as part of a list of
`references, and the District Court did not consider or rely upon the combinations or
`even the art presented in this petition as a basis for its decision. Third, the Decision
`failed to consider the merits of this petition as part of its balanced assessment
`under section 314(a), relying wholesale on the District Court’s order which did not
`address the merits of this petition at all. The burdens of proof differ between the
`forums such that a decision rendered under a more stringent “clear and convincing
`standard” is not dispositive in an IPR where there is no presumption of validity.
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`15
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`Dated June 5, 2019
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`Respectfully Submitted,
`
`/Alexander E. Gasser/
`Alexander E. Gasser (Reg. No. 48,760)
`SKIERMONT DERBY LLP
`1601 Elm Street, Suite 4400
`Dallas, TX 75201
`P: 214-978-6600/F: 214-978-6601
`Lead Counsel for Petitioner
`
`Sarah Spires (Reg. No. 61,501)
`Paul J. Skiermont (pro hac vice to be
`requested)
`SKIERMONT DERBY LLP
`1601 Elm Street, Suite 4400
`Dallas, TX 75201
`P: 214-978-6600/F: 214-978-6601
`
`Mieke Malmberg (pro hac vice to be
`requested)
`SKIERMONT DERBY LLP
`800 Wilshire Blvd., Suite 1450
`Los Angeles, CA 90017
`P: 213-788-4500/F: 213-788-4545.
`
`Back-Up Counsel for Petitioner
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`16
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`CERTIFICATE OF SERVICE
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`I hereby certify that on June 5, 2019, a copy of this Petitioner’s Request for
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`Rehearing under 37 C.F.R. § 42.71(d)(1), including any papers filed therewith, was
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`served by delivering a copy via electronic mail to the attorneys of record for the
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`Patent Owner as follows:
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`Daniel J. Minion (Reg. No. 53,329)
`Dominick A. Conde (Reg. No. 33,856)
`William E. Solander (pro hac vice to be filed)
`Melinda R. Roberts (pro hac vice to be filed)
`Venable LLP
`1290 Avenue of the Americas
`New York, NY 10104-3800
`DMinion@Venable.com
`DConde@Venable.com
`WSolander@Venable.com
`MRRoberts@Venable.com
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`
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`/Alexander E. Gasser/
`
`Alexander E. Gasser (Reg. No. 48,760)
`SKIERMONT DERBY LLP
`1601 Elm Street, Suite 4400
`Dallas, TX 75201
`
`P: 214-978-6600/F: 214-978-6601
`
`17
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