Cyprium Therapeutics, Inc. v. Curia Global, Inc.

2024 NY Slip Op 51698(U)
CourtNew York Supreme Court, Albany County
DecidedDecember 11, 2024
DocketIndex No. 905902-22
StatusUnpublished

This text of 2024 NY Slip Op 51698(U) (Cyprium Therapeutics, Inc. v. Curia Global, Inc.) is published on Counsel Stack Legal Research, covering New York Supreme Court, Albany County primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Cyprium Therapeutics, Inc. v. Curia Global, Inc., 2024 NY Slip Op 51698(U) (N.Y. Super. Ct. 2024).

Opinion

Cyprium Therapeutics, Inc. v Curia Global, Inc. (2024 NY Slip Op 51698(U)) [*1]
Cyprium Therapeutics, Inc. v Curia Global, Inc.
2024 NY Slip Op 51698(U)
Decided on December 11, 2024
Supreme Court, Albany County
Platkin, J.
Published by New York State Law Reporting Bureau pursuant to Judiciary Law § 431.
This opinion is uncorrected and will not be published in the printed Official Reports.


Decided on December 11, 2024
Supreme Court, Albany County


Cyprium Therapeutics, Inc., Petitioner,

against

Curia Global, Inc., Respondent.




Index No. 905902-22

DLA Piper LLP (US)

Attorneys for Petitioner

(Brett Ingerman, of counsel)

650 S. Exeter Street, Suite 1100

Baltimore, Maryland 21202

—and—

(Steven M. Rosato, of counsel)

1251 Avenue of the Americas

New York, New York 10020

Nixon Peabody LLP

Attorneys for Respondent

(Daniel J. Hurteau, of counsel)

677 Broadway, 10th Floor

Albany, New York 12207

Vedder Price P.C.

Co-Attorneys for Respondent

(Richard H. Tilghman, of counsel)

222 North LaSalle Street

Chicago, Illinois 60601
Richard Platkin, J.

Petitioner Cyprium Therapeutics, Inc. ("Cyprium") brought this special proceeding under CPLR 7502 (c), seeking a preliminary injunction in aid of arbitration against respondent Curia Global, Inc. ("Curia"). The Court granted an injunction on September 12, 2022, and the arbitration concluded with an award in Curia's favor on March 8, 2024.

Curia moves by Order to Show Cause dated August 6, 2024, "pursuant to CPLR §§ 6315 and 7511 and 22 NYCRR 130-1.1," for an order directing payment of the undertaking posted by Cyprium, along with monetary sanctions under Part 130 (NYSCEF Doc No. 154).

Cyprium opposes the motion and cross-moves under CPLR 6315 for an order "discharging the undertaking in the amount of $934,400 posted . . . on December 21, 2022" (NYSCEF Doc No. 157).



BACKGROUND

A. Injunction Proceedings

Cyprium commenced this special proceeding on August 4, 2022 for a preliminary injunction in aid of an anticipated arbitration challenging Curia's purported termination of a master services agreement.

"Cyprium is a biotechnology company that develops novel therapies for Menkes disease" (NYSCEF Doc No. 1 ["Petition"], ¶ 36), a rare but severe childhood illness for which there is no treatment approved by the U.S. Food and Drug Administration ("FDA") (see id., ¶ 6). The injectable drug that Cyprium sought to bring to market, Copper Histidinate, was shown to increase patients' average life expectancy from 16 months to nearly 15 years (see id., ¶¶ 6-7).

Cyprium engaged Curia, a "global contract research, development and manufacturing organization that assists biotechnology companies in the development and manufacturing of drug therapies" (id., ¶ 37), to produce the drug for clinical trials. Following successful trials, Cyprium began preparing a new drug application for the FDA's approval. The parties anticipated that Curia would serve as the commercial manufacturer of the drug, and Curia began upgrading its production facility in preparation for the work.

Pursuant to a master services agreement dated December 9, 2021 (see Petition, Ex. 1 ["MSA"]) and two work orders dated February 23, 2022 (see id., Exs. 2-3 ["Work Orders"]), Curia agreed to manufacture two batches of the drug for Cyprium to confirm that the upgrades and modifications to the production facility had not affected the quality of the finished product.

The MSA required Cyprium to make an upfront payment of 30% of the overall value of the Work Orders (see MSA, ¶ 6 [b]; Work Orders, § 7.2) and to "pay each invoice . . . within thirty (30) days of the date such invoice is sent" (MSA, ¶ 6 [c]). However, "[i]f any portion of an invoice is disputed in good faith, [Cyprium] will pay the undisputed amounts and promptly notify Curia in writing of the nature of the dispute, whereupon the parties will use good faith efforts to reconcile the disputed amount as soon as practicable" (id.).

On April 7, 2022, Curia invoiced Cyprium for the Work Orders, calling for payment by May 7, 2022 (see NYSCEF Doc Nos. 25-26 ["Invoices"]). However, disagreements between the parties arose concerning production delays, quality assurance issues, the proposed testing regime and the overarching question of whether Curia would be manufacturing "commercial" batches of the Product, as requested by Cyprium, or producing clinical batches "using commercial production standards," as Curia insisted (Petition, ¶ 54).

At Cyprium's request, a teleconference was held on April 29, 2022. According to Cyprium, no one from Curia "could provide a meaningful explanation for the delays" or for [*2]Curia's position that it was not obliged to test the confirmation batches in accordance with FDA regulations (id., ¶ 61). "Given Curia's apparent inability and unwillingness to deliver the manufacturing services that it promised under the February 23 Work Orders, Cyprium made clear during the April 29th teleconference that no payment on the Disputed Invoices would be forthcoming until the parties' issues were resolved" (id., ¶ 62).

"Curia concluded the [call] by assuring Cyprium that it would meet internally to discuss the disputes and would be in touch shortly with a proposed solution. Instead, the next communication that the parties had regarding this ongoing dispute was Curia's June 9, 2022 Termination Letter" (id., ¶ 63), which stated that Curia was terminating the MSA on account of two material breaches by Cyprium: (1) failure to pay the Invoices, and (2) unauthorized regulatory communications with the FDA (see NYSCEF Doc No. 27).

Cyprium demanded that Curia rescind the termination and continue performing under the MSA (see NYSCEF Doc No. 37), but Curia refused. Cyprium then commenced this special proceeding for a preliminary injunction obliging Curia to continue performing under the MSA during the pendency of anticipated arbitration (see NYSCEF Doc No. 12).

In maintaining that Cyprium was unlikely to prevail in arbitration on its claim that the MSA was wrongfully terminated for non-payment, Curia argued that Cyprium did not object to the Invoices when presented, and it heard nothing from Cyprium about the Invoices until after the Termination Letter. And despite detailed meeting minutes and project notes, there was no record of Cyprium raising a payment dispute or even referring to the Invoices during the April 29, 2022 teleconference.

In a Decision & Order dated September 12, 2022 ("PI Decision"), the Court granted an injunction restraining Curia from terminating the MSA during the pendency of the arbitration (see 81 Misc 3d 1238[A], 2022 NY Slip Op 51426[U] [Sup Ct, Albany County 2022]).

In finding that Cyprium had demonstrated a sufficient likelihood of success in arbitration, the Court relied upon the sworn statements of Cyprium's Petition, as verified by Dr. Lung Yam, the company's chief executive officer:

18.

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Cite This Page — Counsel Stack

Bluebook (online)
2024 NY Slip Op 51698(U), Counsel Stack Legal Research, https://law.counselstack.com/opinion/cyprium-therapeutics-inc-v-curia-global-inc-nysupctalbany-2024.