Therapure Biopharma, Inc. v. DynPort Vaccine Company, LLC

CourtDistrict Court, D. Maryland
DecidedJune 5, 2020
Docket1:19-cv-02092
StatusUnknown

This text of Therapure Biopharma, Inc. v. DynPort Vaccine Company, LLC (Therapure Biopharma, Inc. v. DynPort Vaccine Company, LLC) is published on Counsel Stack Legal Research, covering District Court, D. Maryland primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Therapure Biopharma, Inc. v. DynPort Vaccine Company, LLC, (D. Md. 2020).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF MARYLAND

THERAPURE BIOPHARMA, INC., *

Plaintiff, * Civil Action No. RDB-19-2092 v. *

DYNPORT VACCINE COMPANY * LLC, * Defendant.

* * * * * * * * * * * * * MEMORANDUM OPINION At issue in this case is an agreement between Plaintiff Therapure Biopharma, Inc. (“Plaintiff” or “Therapure”) and Defendant DynPort Vaccine Company LLC (“Defendant” or “DVC”) with respect to a subcontract to provide goods and services in connection with the development of a nerve agent antidote for military and commercial purposes. Therapure alleges that DVC failed to meet its obligations under the parties’ contract and asserts four claims in its Amended Complaint against DVC: breach of contract (Count I); quantum meruit (Count II); and unjust enrichment (Counts III and IV). Presently pending is Defendant’s Motion to Dismiss Plaintiff’s Amended Complaint. (ECF No. 31.) The parties’ submissions have been reviewed, and no hearing is necessary. See Local Rule 105.6 (D. Md. 2018). For the reasons that follow, Defendant’s Motion to Dismiss (ECF No. 31) shall be GRANTED IN PART and DENIED IN PART. Specifically, Counts II, III, and IV will be DISMISSED. BACKGROUND In ruling on a motion to dismiss, this Court “accept[s] as true all well-pleaded facts in a complaint and construe[s] them in the light most favorable to the plaintiff.” Wikimedia Found. v. Nat’l Sec. Agency, 857 F.3d 193, 208 (4th Cir. 2017) (citing SD3, LLC v. Black & Decker (U.S.) Inc., 801 F.3d 412, 422 (4th Cir. 2015)). The Court may consider only such sources outside the complaint that are, in effect, deemed to be part of the complaint, for example, documents

incorporated into the complaint by reference and matters of which a court may take judicial notice. Sec’y of State for Defence v. Trimble Navigation Ltd., 484 F.3d 700, 705 (4th Cir. 2007). Plaintiff Therapure is a privately held business organized and existing under the laws of Ontario, Canada with its principal place of business and headquarters in Mississauga, Ontario. (Am. Compl. ¶ 9, ECF No. 27.) It consists of two business units: (1) a Contract Development and Manufacturing Organization that provides a range of therapeutic protein

development manufacturing services and (2) a product unit “focused on commercializing plasma proteins derived primarily using its proprietary technology.” (Id.) Defendant DVC is a corporation organized under the laws of Virginia, with its principal place of business and headquarters in Frederick, Maryland.1 (Id. ¶ 10.) DVC manages product development programs for the United States and international government entities and provides consulting services to biotechnology and pharmaceutical companies. (Id.)

I. The Basic Ordering Agreement In or around May of 2013, Therapure and DVC entered into a Basic Ordering Agreement (“BOA”), under which Therapure was subcontracted by DVC to provide certain goods and services in support of the development of a nerve agent antidote. (Id. ¶¶ 1, 13, 18; BOA, ECF No. 31-42.) DVC had the prime contract with the Department of Defense

1 This Court has subject matter jurisdiction in this matter pursuant to 28 U.S.C. § 1332(a) and the diversity of citizenship between the parties. 2 The Court may properly consider “any document that the defendant attaches to its motion to dismiss if the document was integral to and explicitly relied on in the complaint and if the plaintiffs do not challenge (“DoD”) to develop the antidote.3 (Am. Compl. ¶ 1.) Therapure alleges that, under the subcontractor’s proposal incorporated by reference in the BOA, the parties agreed to certain assumptions regarding the paste material that would be used in the clinical trials for the

approval of the nerve antidote. (Id. ¶¶ 15, 17, 19.) Specifically, Therapure alleges that the proposal included the following assumptions about the paste: “DVC would deliver Cohn Fraction IV-4 paste, meeting acceptance criteria outlined by Therapure; DVC-procured Cohn Fraction IV-4 paste would be sourced from FDA-approved collection centers, would meet FDA requirements, and would have undergone testing for pathogens; and would meet certain requirements regarding average yield, failure rate, and purity.” (Id. ¶ 17.)

Therapure alleges that the BOA requires DVC to reimburse Therapure for various performance-related costs and that the BOA establishes procedures for Therapure to submit Requests for Equitable Adjustments (“REAs”), seeking recovery of additional unexpected costs for which it believes DVC is liable. (Id. ¶ 20.) The BOA also contains a “quality assurance” provision, requiring that the goods and services are developed according to the terms of the BOA and the applicable task order. (Id. ¶ 21.) In addition, the BOA contains a

“Notice of Delay” provision and “invoice instructions.” (Id. ¶ 22; BOA, ECF No. 31-4.) The Notice of Delay provision provides, “[i]n the event that DVC has knowledge that any actual

its authenticity.” Tucker v. Specialized Loan Servicing, LLC, 83 F. Supp. 3d 635, 648 (D. Md. 2015) (quoting CACI Int’l v. St. Paul Fire & Marine Ins. Co., 566 F.3d 150, 154 (4th Cir. 2009)). The Court will consider the BOA, attached as an exhibit to Defendant’s Motion to Dismiss, because Plaintiff explicitly relies on the BOA in its Amended Complaint: “This action raises out of a basic ordering agreement (‘BOA’ or ‘subcontract’) entered into by Therapure and Defendant in May 2013….” (See Am. Compl. ¶ 13, ECF No. 27.) The Court will also consider the License Agreement (ECF No. 31-5), which Plaintiff also incorporates by reference in the Amended Complaint: “through a separately executed license agreement attached to the BOA, Therapure insisted that Defendant agree that Therapure would retain certain commercial rights to manufacture the developed Bioscavenger product.” (Am. Compl. ¶ 25.) 3 The DoD is not a party to this litigation. situation may delay or threaten to delay the timely performance of this Subcontract…DVC shall, within five (5) business days provide written notification to Therapure’s Project Manager of the nature of the anticipated delay.” (Id.) The invoice instructions provide that DVC

would pay Therapure “the amounts specified” by Therapure “in duly prepared and submitted invoices, subject to the resolution of any questions the Contractor may have about the services performed or amounts invoiced.” (Id.) Finally, Therapure alleges that the BOA contains specific procedures regarding the resolution of disputes, none of which cite, quote, contain, reference, or incorporate the “Disputes Clause” of the Federal Acquisition Regulations (“FAR”), 48 C.F.R. § 52.233-1.

(Am. Compl. ¶ 24.) Instead, Therapure alleges that, under the BOA, “any disputes that do not involve a decision by the contracting officer with respect to the prime contract ‘shall be decided by DVC,’ unless Therapure notified DVC within thirty days that it disagreed with such decision, in which case Therapure ‘may proceed to have the dispute settled through appropriate legal action.’” (Id. ¶ 23.) Therapure alleges that it would not have executed the BOA absent retention of certain commercial rights to manufacture the developed product,

which was also memorialized in a separate License Agreement between Therapure and DVC. (Id. ¶¶ 25, 26; License Agreement, ECF No. 31-5.) Therapure estimates the revenue opportunity associated with these rights as worth approximately $100 million per year. (Id.) II.

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Therapure Biopharma, Inc. v. DynPort Vaccine Company, LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/therapure-biopharma-inc-v-dynport-vaccine-company-llc-mdd-2020.