ROBERT C. JONES, District Judge.
These four consolidated cases arise out of Defendants' application with the Food and Drug Administration ("FDA") to manufacture and sell generic versions of a patented drug. Pending before the Court are a Motion to Stay (ECF No. 463), a Motion to Reconsider (ECF No. 465), two Motions to Strike (ECF Nos. 474, 477), and nine Motions to Seal (ECF Nos. 462, 464, 467, 471, 476, 478, 480, 482, 485).
These cases arise out of the alleged infringement of Plaintiff Ferring B.V.'s ("Ferring") U.S. Patent No. 7,947,739 for tranexamic acid tablets sold under the trademark Lysteda® (the "`739 Patent" or "Tablet Patent"), (see Compl. ¶¶ 13-17, July 7, 2011, ECF No. 1; Compl. ¶¶ 9-13, July 8, 2011, ECF No. 1 in Case No. 3:11-cv-00485), and the alleged infringement of Ferring's U.S. Patent No. 8,022,106 for tranexamic acid formulations and methods of treating menorrhagia therewith (the "`106 Patent" or "Formulas and Treatment Patent"), (see Compl. ¶¶ 13-17, Nov. 25, 2011, ECF No. 1 in Case No. 3:11-cv-00853; Compl. ¶¶ 9-13, Nov. 25, 2011, ECF No. 1 in Case No. 3:11-cv-00854).
The Court consolidated the four cases, with the `481 Case as the lead case. It also granted motions to dismiss the counterclaims for invalidity and to strike affirmative defenses for invalidity in the `481 and `854 Cases, with leave to amend. The Court ruled that affirmative defenses must specify a distinct legal theory of invalidity under Rule 8(c) but need not be pled according to the Iqbal plausibility standard, as the counterclaims must be under Rule 8(a). Watson Defendants and Apotex Defendants amended their answers and counterclaims, accordingly. (See ECF Nos. 93, 94). Apotex Defendants later further amended its answer and counterclaim. The Court denied motions to dismiss the amended counterclaims for invalidity. The Court held a Markman hearing and issued a claim construction order. The Court held a bench trial and gave its findings of fact and conclusions of law from the bench, requesting counsel to draft a written order. The parties have since filed several motions.
Before addressing the other motions, the Court will grant the nine motions for leave to file those motions and related pleadings under seal.
Watson asks the Court to stay judgment pending appeal. The Court denies the motion. Watson argues that Ferring will not be irreparably harmed by a stay because: (1) under an agreement with a third party, Ferring would have saved $12.5 million upon the entry of a generic competitor into the market before May 13, 2013; and (2) the entry of a generic competitor into the market can actually benefit a brand name product, and that is, according to Watson, the case here. As to the first argument, it is not clear whether Ferring was able to take advantage of its alleged contractual provision with the third party. Even if it were so, that issue is settled. Ferring either did or did not avoid the additional $12.5 million payment to the third party based upon Watson's pre-May 13, 2013 marketing of its infringing product. The harm to Ferring going forward is from further competition by an infringing product. Also, even assuming for the sake of argument that all of Ferring's profit from Lysteda could be attributed to Watson's entry into the market, an infringement defendant cannot argue that the patentee has not been harmed by infringement simply because his sales have increased. The harm is not purely economic but also in the loss of good faith with the consuming public that comes from being an innovator with an exclusive product. That good faith carries forward to future endeavors of the company unrelated to the sale of a particular product. Moreover, Watson's argument that as a competitor it actually benefitted Ferring implicitly admits that Watson's marketed product infringed Ferring's patent(s). That admission also severely damages Watson's argument that its ANDA filing did not infringe Ferring's patents under 35 U.S.C. § 271(e)(2). See Glaxo, Inc. v. Novopharm, Ltd., 110 F.3d 1562, 1567-68 (Fed. Cir. 1997) ("The relevant inquiry is whether the patentee has proven by a preponderance of the evidence that the alleged infringer will likely market an infringing product."). Watson has not shown that it is likely to succeed on the merits of the appeal.
This issue is unripe. Because the Court has not yet entered any injunction but only indicated its tentative inclinations, the Court will not "reconsider" entry of a potential future injunction.
First, Watson asks the Court to strike a letter to the Court from Ferring concerning the substantive issue of a request for a preliminary injunction as an improper communication with the Court. The Court denies the motion. As Ferring notes, the letter accompanied the proposed form of judgment the Court requested Ferring to file and did not constitute a request for any separate injunction.
Second, Apotex asks the Court to strike Ferring's proposed findings of fact and conclusions of law as to Apotex, because the Court indicated that it intended to rule in favor of Apotex given Apotex's post-trial agreement to amend its ANDA to exclude the possibility that FDA approval would permit Apotex to sell products within the scope of Ferrings claims. Apotex argues that the Court instructed Ferring and Apotex to agree upon an appropriate stipulation but that Ferring instead simply wrote the proposed judgment as if there were to be no stipulation but Apotex simply lost at trial. The Court addressed the issue at the March 5, 2013 hearing.
IT IS HEREBY ORDERED that the Motions to Seal (ECF Nos. 462, 464, 467, 471, 476, 478, 480, 482, 485) are GRANTED.
IT IS FURTHER ORDERED that the Motion to Stay (ECF No. 463), the Motion to Reconsider (ECF No. 465), and the Motions to Strike (ECF Nos. 474, 477) are DENIED.
IT IS SO ORDERED.