Cellectis S.A. v. Precision Biosciences

883 F. Supp. 2d 526, 2012 WL 3195087, 2012 U.S. Dist. LEXIS 109969
CourtDistrict Court, D. Delaware
DecidedAugust 6, 2012
DocketCiv. No. 11-173-SLR
StatusPublished
Cited by4 cases

This text of 883 F. Supp. 2d 526 (Cellectis S.A. v. Precision Biosciences) is published on Counsel Stack Legal Research, covering District Court, D. Delaware primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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Cellectis S.A. v. Precision Biosciences, 883 F. Supp. 2d 526, 2012 WL 3195087, 2012 U.S. Dist. LEXIS 109969 (D. Del. 2012).

Opinion

MEMORANDUM OPINION

SUE L. ROBINSON, District Judge.

I. INTRODUCTION

Plaintiff Cellectis S.A. (“Cellectis”) filed the present action against defendant Precision Biosciences, Inc. (“Precision”) on March 1, 2011, alleging infringement of U.S. Patent No. 7,897,372 (“the '372 patent”), which is assigned to Cellectis. (D.I. 1) The '372 patent, entitled “I-Cre 1 Mega-nuclease Variants with Modified Specificity, Method of Preparation and Uses Thereof,” is directed to particular I-Cre 1 meganucleases having mutations that permit binding and cleavage of DNA at specific sites. (Id. at ¶ 8) Currently before the court is Precision’s motion to stay the present litigation pending the completion of ex parte reexamination of the '372 patent. (D.I. 41) Also before the court is Precision’s motion for leave to amend its answer and counterclaims to add allegations of inequitable conduct in the procurement of the '372 patent. (D.I. 113) For the reasons that follow, the court denies both motions.

II. BACKGROUND

A. Procedural Posture

The litigation history between Cellectis and Precision is extensive. In March of 2008, Cellectis sued Precision in the United States District Court for the Eastern District of North Carolina for infringement of U.S. Patent Nos. 6,610,545 (“the '545 patent”) and 7,309,605 (“the '605 patent”). See Cellectis S.A. v. Precision BioSciences, Inc., Civ. No. 08-118 (E.D.N.C.) (“North Carolina I ”). The '545 and '605 patents each issued from an application first filed by Institut Pasteur in 1992, and relate to DNA encoding the meganuclease I-Scel. Subsequent to the initiation of suit, Precision requested, and was granted, inter partes reexamination of the '545 and '605 [529]*529patents. Precision filed a motion to stay North Carolina I, which motion was granted in August 2010 at the close of fact discovery. (D.I. 23 at 6) The United States Patent and Trademark Office (“PTO”) has since rejected the claims of the '545 and '605 patents, and the Board of Patent Appeals and Interferences affirmed the rejection.1

On March 1, 2011 at 5:59 a.m., as soon as U.S. Patent No. 7,897,372 (“the '372 patent”) issued and was publicly available from the PTO’s website, Celleetis filed the instant litigation against Precision for infringement of the '372 patent.2 Later that same day, Precision filed a declaratory judgment action on the '372 patent in North Carolina (E.D.N.C. Civ. No. 11-91 (“North Carolina II ”)).

On March 22, 2011, Celleetis filed a motion to enjoin Precision from prosecuting its declaratory judgment actions. (D.I. 7)3 Thereafter, Precision answered the complaint in this action and asserted affirmative defenses and counterclaims of non-infringement and invalidity of the '372 patent. (D.I. 10) On April 8, 2011, Precision filed a motion to transfer the present action to the United States District Court for the Eastern District of North Carolina. (D.I. 16)

On April 18, 2011, Celleetis amended its complaint in this action and added claims of unfair competition (“count II”) and violations of the Lanham Act, 15 U.S.C. § 1125(a) (“count III”), each relating to allegedly false and misleading commercial representations on Precision’s website. (D.I. 22 at ¶¶ 15-19, 24-31) Precision filed a Request for Ex Parte Reexamination of the '372 patent with the PTO on April 29, 2011. (D.I. 42 at 6) Precision filed its answer to Cellectis’s amended complaint on May 5, 2011, adding a third affirmative defense that Celleetis is barred from relief on counts II and III of its amended complaint “in whole or in part by laches, estoppel and/or other equitable doctrines.” (D.I. 27 at 5) The court entered a scheduling order on May 17, 2011. (D.I. 33)

The PTO granted Precision’s request for ex parte reexamination of the '372 patent on July 8, 2011 and, on August 8, 2011, Precision filed a motion to stay the present suit pending the outcome of that proceeding. (D.I. 41; D.I. 42 at 1, 6) On December 6, 2011, Celleetis filed a request for a certificate of correction for the '372 patent to change its claim of priority under 35 U.S.C. § 119 to a claim of priority under 35 U.S.C. § 120. (D.I. 113, ex. A at ¶ 31) The PTO issued the certificate on January 10, 2012.

Discovery has since proceeded in the litigation. On March 28, 2012, Precision moved for leave to amend its answer to add claims of inequitable conduct in the procurement of the '372 patent. (D.I. 113) On May 3, 2012, upon consideration of all of the relevant factors, the court found that Precision did not tip the scales in favor of transferring the case to North Carolina, and denied Precision’s motion to transfer. (D.I. 134; D.I. 135) The court also found that the instant suit (Civ. No. 11-173) was the first-filed case vis a vis North Carolina II. Insofar as none of the [530]*530exceptions to the first-filed rule were applicable, the court granted Cellectis’ motion to enjoin the North Carolina litigation. (Id.)

B. The '372 Patent

The '372 patent, entitled “I-Oe 1 Mega-nuclease Variants with Modified Specificity, Method of Preparation and Uses Thereof,” is directed to particular mutated I-Oe 1 meganucleases that bind and- cleave DNA at specific sites. The '372 patent issued from U.S. Patent Application Serial No. 11/908,798 (“the 798 application”), the U.S. phase application under 35 U.S.C. § 271 of PCT No. PCT/IB2006/001203, filed March 15, 2006 (hereinafter, the “Parent PCT”). The Parent PCT, in turn, claimed priority to two foreign applications: (1) PCT/IB2005/000981 (March 15, 2005); and (2) PCT/IB2005/003083 (September 19, 2005). The '372 patent names two inventors: Philippe Duchateau (“Du-chateau”); and Frederic Paques (“Pa-ques”).

C. Reexamination Status

The PTO mailed its initial Office Action rejecting all claims (1-54) of the '372 patent on January 18, 2012. Therein, the examiner rejected claims 1-10, 13-16, 19-28, 31-34, 37-46 and 49-52 as anticipated under 35 U.S.C. § 102(e) by another Cellectis patent application, WO 2004/067736 by Arnould et al. (“Arnould”). (D.I. 70) Arnould is a PCT (international) application bearing a filing date of January 28, 2004; priority is claimed to two United States publications published January 28, 2003 and August 1, 2003.4 (D.I. 113, ex. 1) Arnould lists several inventors: (1) Du-chateau; (2) Paques; (3) Sylvain Arnould (“S. Arnould”); (4) Jean-Pierre Cabaniols; (5) Patrick Chames (“Chames”); (6) Andre Choulika; Jean-Charles Epinat (“J.C. Epinat”); (7) Emmanuel LaCroix (“LaCroix”); (8) Christophe Pere^-Michaut; (9) Julianne Smith; and (10) David Sourdive. (Id.)

The examiner asserts that Arnould discloses SEQ ID 70 as claimed in independent claim 1, as Arnould’s SEQ ID 5 (Fig. 2C) encodes the first 164 residues of this sequence. (D.I. 116, ex. 9 at p.

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883 F. Supp. 2d 526, 2012 WL 3195087, 2012 U.S. Dist. LEXIS 109969, Counsel Stack Legal Research, https://law.counselstack.com/opinion/cellectis-sa-v-precision-biosciences-ded-2012.