Forest Laboratories, Inc. And Ony, Inc. v. Abbott Laboratories, and Tokyo Tanabe Company, Ltd.

339 F.3d 1324, 67 U.S.P.Q. 2d (BNA) 1682, 2003 U.S. App. LEXIS 16170, 2003 WL 21804831
CourtCourt of Appeals for the Federal Circuit
DecidedAugust 7, 2003
Docket03-1067
StatusPublished
Cited by101 cases

This text of 339 F.3d 1324 (Forest Laboratories, Inc. And Ony, Inc. v. Abbott Laboratories, and Tokyo Tanabe Company, Ltd.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Federal Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Forest Laboratories, Inc. And Ony, Inc. v. Abbott Laboratories, and Tokyo Tanabe Company, Ltd., 339 F.3d 1324, 67 U.S.P.Q. 2d (BNA) 1682, 2003 U.S. App. LEXIS 16170, 2003 WL 21804831 (Fed. Cir. 2003).

Opinion

LOURIE, Circuit Judge.

Abbott Laboratories appeals from the decision of the United States District Court for the Western District of New York awarding attorney fees and expenses to ONY, Inc. and Forest Laboratories, Inc. based on Abbott’s conduct that led to a holding of equitable estoppel. Forest Labs., Inc. v. Abbott Labs., No. 96-CV-159A (W.D.N.Y. Sept. 4, 2001) (“Forest TV”). Because we conclude that the court erred in finding this case to be “exceptional” under 35 U.S.C. § 285, we reverse.

BACKGROUND

Tokyo Tanabe Company, Ltd. owns U.S. Patents 4,338,301 and 4,397,839, which are directed to a lung surfactant composition for treating respiratory distress syndrome in premature babies. Pursuant to an exclusive license of the '301 and '839 patents, Abbott developed a commercial product known as Survanta® in the 1980s. At about the same time, ONY developed its own product for treating neonatal respiratory distress syndrome called Calf Lung Surfactant Extract (“CLSE”). In June 1991, ONY entered into an agreement with Forest for Forest to further develop and market CLSE under the trade name Infa-surf®.

From 1983 until 1991, Abbott and ONY maintained contact regarding the development of CLSE. Abbott met with ONY in November 1983 to discuss the development, composition, and testing of CLSE, and later informed ONY that it had opted to develop the Tanabe product instead of CLSE because the Tanabe product had patent protection. In April 1984, at Abbott’s request, ONY submitted a memorandum of invention to Abbott disclosing “everything known about CLSE” for Abbott to conduct a patentability search. Upon completion of the search, Abbott informed ONY that CLSE was likely not patentable in light of two “pertinent references,” but did not mention the '301 and '839 patents; nonetheless, Abbott encouraged ONY that it “look[ed] forward to working with [ONY] in the future.” In April 1986, Abbott again met with ONY to discuss the possibility of joint development of CLSE and suggested that “some future collaboration” might still be possible. Abbott continued to monitor the development of CLSE until 1991, while internally expressing concern that ONY might receive FDA approval for CLSE before Abbott could do so for Survanta®.

In July 1991, Abbott received both FDA approval and orphan drug status (providing seven years’ market exclusivity) for Survanta®, which it then proceeded to market. Several years later, Abbott informed ONY and Forest that it had reason to believe that Infasurf® would infringe the '301 and '839 patents if it were to be marketed. Nonetheless, in March 1995, ONY filed a new drug application for approval to market Infasurf®. The FDA then notified ONY that Infasurf® was the “same drug” as Survanta® under the Orphan Drug Act, 21 U.S.C. §§ 360aa-360dd (1994), and that it therefore could not be approved for sale until Abbott’s period of exclusivity expired in July 1998.

In light of Abbott’s June 1994 letter claiming infringement and the FDA’s noti *1327 fication that Infasurf® and Survanta® were the “same drug,” ONY and Forest sued Abbott and Tanabe in the U.S. District Court for the Western District of New York, seeking a declaratory judgment of noninfringement and invalidity of the '301 and '839 patents. Abbott and Tanabe counterclaimed for infringement. A jury found both patents infringed and not invalid and, in an advisory verdict, rejected ONY and Forest’s defense of equitable estoppel. The district court, however, granted ONY and Forest a judgment of noninfringement as a matter of law (“JMOL”) on the ground that Abbott and Tanabe had failed to present any evidence at trial to show that CLSE met the water content limitations of the patents in suit either literally or under the doctrine of equivalents. Forest Labs., Inc. v. Abbott Labs., No. 96-CV-159A, 1999 U.S. Dist. LEXIS 23217, at *20-21, 1999 WL 33299123 (W.D.N.Y. June 23, 1999) (“Forest I”). In a separate opinion, the court also ruled that Abbott, and Tanabe by imputation, was equitably estopped from asserting infringement of the '301 and '839 patents against ONY and Forest because: (1) Abbott, in bad faith, misled ONY and Forest to believe that it would not assert infringement by encouraging their development of Infasurf® and by neglecting its duty to inform them of any possible infringement; (2) ONY and Forest reasonably relied on Abbott’s misleading conduct; and (3) ONY and Forest would suffer economic and evidentiary prejudice if Abbott were permitted to proceed with its infringement counterclaim. Forest Labs., Inc. v. Abbott Labs., No. 96-CV-159A, 1999 U.S. Dist. LEXIS 23215, at *25-26 (W.D.N.Y. June 23, 1999) (“Forest II”). On appeal, we affirmed the JMOL of non-infringement and, having done so, declined to consider the equitable estoppel issue. Forest Labs., Inc. v. Abbott Labs., 239 F.3d 1305, 1314 (Fed.Cir.2001) (“Forest III”).

The district court subsequently granted ONY and Forest’s motion for attorney fees and expenses against Abbott, but not Tan-abe. The court found the case to be “exceptional” under 35 U.S.C. § 285 because Abbott, in bad faith, encouraged ONY to develop CLSE, disregarded its duty to advise ONY and Forest of possible infringement, and pursued its infringement counterclaim with a “reckless disregard for the facts in an attempt to prevent Infasurf from reaching the market.” Forest IV, slip op. at 12. In so finding, the court rejected Abbott’s argument that fees could not be awarded for bad-faith conduct that occurred prior to litigation and held that, in any event, Abbott had acted in bad faith during litigation by bringing suit with knowledge of its prior bad-faith conduct toward ONY and Forest. Id. at 11. Having found the case to be exceptional, the court then chose to exercise its discretion and award attorney fees in order to avoid a “gross injustice” and to deter patentees from similar bad-faith conduct in the future. Id. at 15. Upon the parties’ stipulation as to the amount of any fee award, the court entered an award against Abbott of $6.5 million in attorney fees and expenses. Forest Labs., Inc. v. Abbott Labs., No. 96-CV-159A (W.D.N.Y. Sept. 30, 2002).

Abbott timely appealed the fee award to this court. We have jurisdiction pursuant to 28 U.S.C. § 1295(a)(1).

DISCUSSION

A determination whether to award attorney fees under 35 U.S.C. § 285 involves a two-step process. First, a district court must determine whether the prevailing party has proved by clear and convincing evidence, Ruiz v. A.B. Chance Co., 234 F.3d 654, 669 (Fed.Cir.2000), that the case is “exceptional.” 35 U.S.C. § 285 (2000); Cybor Corp. v. FAS Techs.,

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339 F.3d 1324, 67 U.S.P.Q. 2d (BNA) 1682, 2003 U.S. App. LEXIS 16170, 2003 WL 21804831, Counsel Stack Legal Research, https://law.counselstack.com/opinion/forest-laboratories-inc-and-ony-inc-v-abbott-laboratories-and-tokyo-cafc-2003.