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`BEFORE THE PATENT TRIAL AND APPEAL BOARD
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`TEVA PHARMACEUTICALS USA, INC.,
`Petitioner
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`V.
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`CORCEPT THERAPEUTICS, INC.
`
`Patent Owner
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`Case PGR2019-00048
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`Patent No. 10,195,214 B2
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`DECLARATION OF UMA N. EVERETT IN SUPPORT OF PETITIONER’S
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`MOTION FOR PRO HAC VICE ADMISSION
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`TEVA1 061
`Teva v. Corcept
`PG R201 9-00048
`
`TEVA1061
`Teva v. Corcept
`PGR2019-00048
`
`
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`PGR2019—00048
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`US. Patent No. 10,195,214
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`1, Uma N. Everett, declare as follows:
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`1.
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`I am a Director with the law firm of Sterne Kessler Goldstein & Fox
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`PLLC. I represent and advise Petitioner Teva Pharmaceuticals USA, Inc. (“Teva”)
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`in connection with the above—captioned post grant review (“PGR”) proceeding. I
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`also represent Teva in connection with the underlying district court litigation
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`(Corcept Therapeutics, Inc. v. Teva Pharmaceuticals USA, Inc, No. 1:18-cv—
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`03632 (D.N.J.)) on the patent at issue in this PGR proceeding, 10,195,214 (“the
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`’214 patent”).
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`2.
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`I have been a member in good standing of the Bar of the District of
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`Columbia since 2002. I am admitted to practice in several US. district courts, the
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`US. Court of Appeals for the Federal Circuit, and the Third Circuit.
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`3.
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`I have not been suspended or disbarred from practice before any court
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`or administrative body.
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`4.
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`No sanction or contempt citation has been imposed against me by any
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`court or administrative body.
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`5.
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`I have never had an application for admission to practice before any
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`court or administrative body denied.
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`6.
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`I practice litigation, primarily patent litigation, and have done so
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`throughout my career as an attorney. I have litigated dozens of patent cases across
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`the country, including in Delaware, New Jersey, and the International Trade
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`-1-
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`
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`IPR2019—00048
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`U.S. Patent No. 10,195,214
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`Commission.
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`7.
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`I have extensively reviewed the ’214 patent, its prosecution history
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`and related materials, and the Patent Owner’s infringement contentions served in
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`the litigation against Teva. Additionally, I worked on Petitioner’s invalidity
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`contentions in the litigation, and accordingly have gained significant familiarity
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`with the invalidity issues in that case. These issues significantly overlap with the
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`corresponding issues in this PGR proceeding. My involvement in the concurrent
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`litigation has made me very familiar with the proposed invalidity grounds and the
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`cited references in this proceeding.
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`8.
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`In this PGR proceeding, I have worked with lead counsel and backup
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`counsel named in this proceeding to identify and analyze the references relied upon
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`in the petition and to assist with drafting the petition.
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`9.
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`The prior-art references at issue in the PGR proceeding are also
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`relevant in the underlying litigation in the case against Teva, and I have reviewed a
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`vast amount of additional, related prior art for the invalidity contentions in the
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`district-court litigation.
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`10.
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`I have conferred with Dr. Greenblatt, and I thoroughly understand Dr.
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`Greenblatt’s testimony related to prior-art publications cited in this PGR
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`proceeding.
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`11.
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`Since 2005, I have represented pharmaceutical companies in
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`
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`IPR2019—00048
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`U.S. Patent No. 10,195,214
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`connection with multiple patent litigations regarding various technologies,
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`including, but not limited to, the mifepristone drug product at issue in this PGR.
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`This includes the following recent litigations:
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`Par Pharm, Inc. v. American Regent, Inc, No. 1:19—cv-Ol490 (DED);
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`Cipla Ltd. v. AstraZeneca A.B., Nos. 1:19-cv—00733, 1:19-cv—00438 (DNJ);
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`Celgene Corporation v. Cipla Ltd, Nos. 2:18—cv-08964, 2:17—cv—06l63
`(DNJ);
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`Meda Pharm. Inc. v. Perrigo UK FINCO Ltd. P ’Ship, No. 1:16—cv—00794
`(DED);
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`.Meda Pharm. Inc. v. Apotex Inc, No. 1:14-cv-01453 (DED);
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`Auxilum Pharm. Inc. v. Upsher-Smith Labs, Inc. Nos. l—l.3—cv-00148, 1-08—
`cv—00908 (DED);
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`Endo Pharm. Inc. v. Amneal Pharm, LLC, No. 1:12—cv~081 15 (SDNY) ;
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`Lithium Silicate Materials & Prods. Containing the Same, 337—TA—911
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`(ITC); and
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`Corcept Therapeutics, Inc. v. Teva Pharm. USA, Inc, No. 2:18—cv—03632
`(DNJ).
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`12.
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`Through this work, I have developed in—depth knowledge of the
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`relevant issues in this proceeding. This knowledge includes my analysis of a
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`significant number of patents, articles, books, and other materials regarding these
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`technologies. My experience also includes knowledge gained from working closely
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`with several technical experts from academia and industry. And I have participated
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`in meetings with Teva’s in—house employees regarding various technologies and
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`applications, including, for example, as related to mifepristone.
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`_3_
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`
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`IPR2019-00048
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`US. Patent No. 10,195,214
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`13. Within the past three years, I have requested to appear pro hac vice
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`before the Office in Argentum Pharmaceuticals LLC et a] v. Cz’pla Limited 61 al.,
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`IPR2017—00807 (PTAB), and my request was granted.
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`14.
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`I have read and will comply with the Office Patent Trial Practice
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`Guide and the Board’s Rules of Practice for Trials set forth in part 42 of the Code
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`of Federal Regulations.
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`15.
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`I understand that I will be subject to the USPTO Rules of Professional
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`Conduct set forth in 37 C.F.R. §§ 11.101 et seq. and disciplinary jurisdiction
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`pursuant to 37 C.F.R. § 11.19(a).
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`16.
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`I hereby declare that all statements made herein of my own
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`knowledge are true and that all statements made on information and belief are
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`believed to be true. I further declare that these statements were made with the
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`knowledge that Willfill false statements and the like so made are punishable by fine
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`or imprisonment, or both, under Section 1001 of Title 18 of the United States Code
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`and that such willful false statements may jeopardize the validity of this
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`proceeding.
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`Respectfully submitted,
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`
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`Date:
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`l'll“l 1
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`
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`District of Columbia, SS.
`ed and Sworn to bet ,re m-
`Subscri
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`
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`N e' NN-WHITE
`EARN ESTEE
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`Notary Public. District of Columbia
`My commission expires May 31, 2023
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