CSL Behring, LLC v. Bayer Healthcare, LLC

CourtDistrict Court, D. Delaware
DecidedSeptember 17, 2019
Docket1:18-cv-00170
StatusUnknown

This text of CSL Behring, LLC v. Bayer Healthcare, LLC (CSL Behring, LLC v. Bayer Healthcare, LLC) 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.

Bluebook
CSL Behring, LLC v. Bayer Healthcare, LLC, (D. Del. 2019).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF DELAWARE ) CSL BEHRING, LLC, ) Plaintiff, V. Civ. No. 18-170-RGA BAYER HEALTHCARE, LLC, ) ) Defendant. ) a)

MEMORANDUM Plaintiff CSL Behring, LLC and Defendant Bayer Healthcare, LLC are parties to a License and Supply Agreement (the “Supply Agreement”) that memorialized Bayer’s obligation to supply CSL with recombinant Factor VIII, a human blood factor used to treat hemophilia A patients. Previously, CSL moved to dismiss Counts 2 and 3 of Bayer’s counterclaims, which alleged breach of contract under the Uniform Commercial Code (“U.C.C.”) and breach of the implied covenant of good faith and fair dealing. (D.I. 31). I granted the motion with leave to amend, and Bayer filed amended counterclaims. (D.I. 69, D.I. 70, D.I. 75). Currently pending before the court is CSL’s motion to dismiss the same claims in Bayer’s amended counterclaims. (D.I. 77). The court has jurisdiction over this matter pursuant to 28 U.S.C. §§ 1331 and 1338(a). For the reasons discussed below, CSL’s motion to dismiss the amended counterclaims is granted.

I. BACKGROUND A. The Parties’ Relationship The Supply Agreement is governed by New York law and terminated by its own terms on December 31, 2017. (D.I. 78-1 at §§ 7.1, 11.2). Under the Supply Agreement, Bayer agreed to manufacture and supply CSL with two human recombinant Factor VIII products that CSL sold under the trade names “Helixate” and “Iblias.” (D.I. 75 at 4 41-44). Bayer concurrently made and sold the same products for itself under the trade names “Kogenate” and “Kovaltry.” (/d.). In May 2016, CSL obtained FDA approval of its own human recombinant Factor VIII product that competes with Helixate and is sold under the trade name “Afstyla.” (/d. at 70). B. Relevant Terms of the Supply Agreement Two provisions in the Supply Agreement govern CSL’s purchasing obligations. First, there is a “minimum purchase obligation,” found in Section 2.2.3.2 of the Supply Agreement, which states: “For Calendar Year 2011 and beyond, CSL’s minimum purchase obligation will be sixty percent (60%) of the previous Calendar Year’s actual purchase.” (D.I. 78-1 at § 2.2.3.2). Second, there is a mechanism set forth in Section 2.3.1 by which CSL provides Bayer, on a monthly basis, rolling forecasts that govern CSL’s future orders. (/d. at § 2.3.1). The first three months of each forecast are considered a “firm order.” (/d.). The second three months (i.e., months four through six) cannot change by more than 15% when those months become firm orders. (/d.). Specifically, Section 2.3.1 states, in relevant part: CSL shall provide Bayer with a rolling twelve (12) month forecast of its requirements of Product broken down by calendar months. .... The first three (3) calendar months of this forecast shall represent a firm order .... The second three (3) calendar months of this forecast may not change more than plus or minus fifteen percent (15%) from the immediately preceding twelve (12) month forecast when the second three (3) months of the immediately preceding forecast are upgraded to the status of a firm order.

Il. STANDARD OF REVIEW Under Rule 12(b)(6), a party may move to dismiss a complaint for failure to state a claim upon which relief can be granted. Fed. R. Civ. P. 12(b)(6). To survive the motion to dismiss, the complaint must contain sufficient factual matter “to state a claim to relief that is plausible on its face.” Ashcroft v. Iqbal, 556 U.S. 662, 677-78 (2009) (quoting Bell Atl. Corp. v. Twombly, 550 U.S. 544, 570 (2007)). The factual allegations do not have to be detailed, but they must provide more than labels, conclusions, or a “formulaic recitation” of the claim elements. Twombly, 550 U.S. at 555. In assessing the plausibility of a claim, the court must accept all well-pleaded factual allegations in the complaint as true and draw all reasonable inferences in favor of the plaintiff. Jn re Rockefeller Ctr. Prop., Inc. Sec. Litig., 311 F.3d 198, 215 (3d Cir. 2002). The court’s review is limited to the allegations in the complaint, exhibits attached to the complaint, documents incorporated by reference, items subject to judicial notice, and matters of the public record. Mayer v. Belichick, 605 F.3d 223, 230 (3d Cir. 2010). Il. DISCUSSION Bayer asserts amended counterclaims for breach of contract based on U.C.C. § 2-306 (Count 2) and breach of the implied covenant of good faith and fair dealing (Count 3). CSL has moved to dismiss both counts for failure to state a claim pursuant to Rule 12(b)(6). Each count is addressed in turn. A. Count 2: Breach of Contract — U.C.C. § 2-306 In Count 2 of the amended counterclaims, Bayer alleges that the Supply Agreement is a “requirements contract” under U.C.C. § 2-306, which CSL breached by failing to order the amount of Helixate that CSL could have sold in calendar year 2017. (D.I. 75 at §§ 107-08). An agreement is not a requirements contract unless it: (1) obligates the buyer to buy the goods exclusively from

the seller, and (2) obligates the buyer to buy all of its requirements for goods of a particular kind from the seller. Jn re Hawker Beechcraft, Inc., 2013 WL 2663193, at *4 (Bankr. S.D.N.Y. June 13, 2013). I previously dismissed this counterclaim, because Bayer failed to show an express or implied promise of exclusivity. (D.I. 69 at 6). With the amended counterclaims, Bayer tries to establish an express or implied promise primarily through extrinsic evidence, specifically allegations regarding its exclusive manufacturing license and the prior course of dealings between the parties and their predecessors. (D.I. 75, Counterclaims at §§ 12-45). Bayer also tries to establish a promise of exclusivity through intrinsic evidence, specifically terms of the Supply Agreement providing for remedies and quantities. For the reasons described below, neither the extrinsic evidence nor the intrinsic evidence can establish that the Supply Agreement is a requirements contract. 1. Extrinsic Evidence According to Bayer, I am obligated by U.C.C. § 2-202 to consider the extrinsic evidence even if the contract is not ambiguous. (D.I. 82 at 8-14). In general, Section 2-202 provides that the terms of a contract may be supplemented, but not contradicted, by extrinsic evidence related to the parties’ course of performance, course of dealing, or usage of trade. Specifically, it states in relevant part: Terms with respect to which the confirmatory memoranda of the parties agree or which are otherwise set forth in a writing intended by the parties as a final expression of their agreement with respect to such terms as are included therein may not be contradicted by evidence of any prior agreement or of a contemporaneous oral agreement but may be explained or supplemented (a) by course of performance, course of dealing, or usage of trade (Section 1-303).... N.Y. U.C.C. § 2-202(a) (emphasis added).

Section 2-202, however, bars the use of extrinsic evidence when the contract at issue is fully integrated. An annotation to Section 2-202 states: “Writings which are a complete ‘integration’ of the parties’ agreement may not be supplemented, contradicted, or varied by parol evidence under the Code and the New York cases.” New York Annotation 1 to N.Y. U.C.C. § 2- 202; see also W. 63 Empire Assocs., LLC v.

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CSL Behring, LLC v. Bayer Healthcare, LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/csl-behring-llc-v-bayer-healthcare-llc-ded-2019.