United Therapeutics Corp. v. Liquidia Techs., Inc.

2025 NCBC 37
CourtNorth Carolina Business Court
DecidedJuly 29, 2025
Docket21-CVS-4094
StatusPublished

This text of 2025 NCBC 37 (United Therapeutics Corp. v. Liquidia Techs., Inc.) is published on Counsel Stack Legal Research, covering North Carolina Business Court primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
United Therapeutics Corp. v. Liquidia Techs., Inc., 2025 NCBC 37 (N.C. Super. Ct. 2025).

Opinion

United Therapeutics Corp. v. Liquidia Techs., Inc., 2025 NCBC 37.

STATE OF NORTH CAROLINA IN THE GENERAL COURT OF JUSTICE SUPERIOR COURT DIVISION DURHAM COUNTY 21CVS004094-310

UNITED THERAPEUTICS CORPORATION and LUNG BIOTECHNOLOGY PBC, ORDER AND OPINION ON Plaintiffs, DEFENDANT LIQUIDIA TECHNOLOGIES, INC.’S MOTION v. FOR SUMMARY JUDGMENT LIQUIDIA TECHNOLOGIES, INC. [PUBLIC] 1 and ROBERT ROSCIGNO,

Defendants.

1. Dr. Robert Roscigno (Roscigno) spent a decade working with United

Therapeutics Corporation (UTC) to develop a therapy for pulmonary arterial

hypertension (PAH) using the drug treprostinil. When he resigned in June 2007,

UTC alleges that he left with a number of documents that UTC contends contain

trade secrets chronicling its drug development efforts. Some eight years later

Roscigno joined a competitor, Liquidia Technologies, Inc. (Liquidia), to lead that

company in its development of an inhaled treprostinil treatment for PAH. UTC

alleges that Roscigno used its trade secrets while employed by Liquidia, giving

Liquidia an impermissible head start in its drug development efforts. Liquidia now

moves for summary judgment arguing, among other things, that the documents at

1 Because certain materials referenced in this Order and Opinion were filed under seal, the Court’s ruling was provisionally filed under seal on 23 July 2025. The Court then permitted counsel for the parties to confer and advise the Court whether they contend any matters referenced herein should be sealed. Having afforded the parties this opportunity, the Court now files its Order and Opinion on the public record. issue do not contain trade secrets. (Liquidia Technologies, Inc’s Motion for Summary

Judgment [Motion], (ECF No. 284).)

2. Having considered the Motion, the related briefing, the arguments of

counsel at a hearing on the Motion, and other appropriate matters of record, the

Court concludes that the Motion should be DENIED.

Brooks, Pierce, McLendon, Humphrey & Leonard, L.L.P, by Eric M. David, Jim W. Phillips, Jr., Kasi W. Robinson, and Sarah N. Schiavone; McDermott Will & Emery LLP, by Douglas H. Carsten, Arthur P. Dykhuis, Katherine Pappas, Joshua Revilla, Courtney Seams, and Lillian J. Spetrino; and Goodwin Proctor LLP, by William C. Jackson, for Plaintiffs United Therapeutics Corporation and Lung Biotechnology PBC.

Parker Poe Adams & Bernstein LLP, by Stephen V. Carey, Corri A. Hopkins, and Andrew P. Tabeling; and Cooley, LLP, by Jonathan Davies, Sanya Sukduang, Lauren Strosnick, Adam Pivovar, Rachel L. Preston, Phillip Morton, Daniel Knauss, and Kyung Taeck Minn, for Defendant Liquidia Technologies, Inc.

McGuireWoods LLP, by David E. Finkelson, Miles O. Indest, Mark E. Anderson, Corrine S. Hockman, and Kyle S. Smith, for Defendant Robert Roscigno.

Earp, Judge.

I. FACTUAL BACKGROUND

3. The Court does not make findings of fact when ruling on a motion for

summary judgment. Instead, the Court summarizes below the material facts it

considers to be uncontested and those facts on which a material dispute forecloses

summary adjudication. See, e.g., Vizant Techs., LLC. v. YRC Worldwide, Inc., 373

N.C. 549, 551 (2020); Ehmann v. Medflow, Inc., 2017 NCBC LEXIS 88, at *6 (N.C.

Super. Ct. Sept. 26, 2017). Roscigno’s Employment with UTC

4. Plaintiffs UTC and Lung Biotechnology PBC (collectively UTC) and

Defendant Liquidia are competitors in the development of treatments for PAH, a rare

disease involving abnormally high blood pressure in the lungs. Elevated pressure

strains the right side of the heart as it pumps blood to the lungs and ultimately could

lead to heart failure. (See Vallerie V. McLaughlin, et al., Addition of Inhaled

Treprostinil to Oral Therapy for Pulmonary Arterial Hypertension, 55 J. AM. COLL.

CARDIOLOGY (2010), ECF No. 285.1; UTC Annual Report (Form 10-K), ECF No.

256.3.) While there is no cure for PAH, the U.S. Food and Drug Administration (FDA)

has approved several drugs for its treatment. (See, e.g., Flolan Prescribing Info., ECF

No. 285.2; Ventavis Prescribing Info., ECF No. 285.3.)

5. Roscigno was employed by UTC from 1997 to 2007. 2 (Def. Robert

Roscigno’s Aff. Supp. Mot. Summ. J. [Roscigno Aff.] ¶ 3, ECF No. 212.6 (under seal),

ECF No. 376 (public version).) At the start of his employment, Roscigno was involved

in the clinical development of Remodulin®, a PAH treatment with the active

ingredient treprostinil. (Excerpts of Sept. 20, 2023 Dep. of Robert Roscigno [Pls.’

Roscigno Dep.] 283:2−8, ECF No. 303.7 (under seal), ECF No. 366.7 (public version).)

UTC first received FDA approval for subcutaneous administration of Remodulin® in

2002, followed by approval for intravenous administration in 2004. (Remodulin®

2 Roscigno served as the Senior Vice President and then President of Lung Rx, Inc., a wholly owned subsidiary of UTC. Plaintiff Lung Biotechnology PBC is the successor-in-interest to Lung Rx, Inc. (Pls.’ Roscigno Dep. 22:18−23:1; Second Am. Compl. ¶ 14, ECF No. 154 (under seal), ECF No. 155 (public version).) Prescribing Info. (2002), ECF No. 285.10; Remodulin® Prescribing Info. (2004), ECF

No. 285.11.)

6. After successfully obtaining FDA approval for Remodulin®, UTC sought

to develop an inhaled treprostinil treatment for PAH. It tasked Roscigno with

overseeing this work. (Pls.’ Roscigno Dep. 23:2−24:1.) Roscigno designed protocols,

collaborated with pharmacokinetic consultants, participated in meetings with

regulators, and oversaw the program budget. (Pls.’ Roscigno Dep. 25:1−27:17; see

also Aff. and Expert Report of David W. Feigal [Feigal Report] ¶ 87, ECF No. 255.17

(under seal), ECF No. 335.17 (public version).) 3

7. UTC ultimately succeeded in its efforts. In 2009, it received FDA

approval for Tyvaso®, an inhaled treprostinil treatment delivered through a

nebulizer. (Tyvaso® Prescribing Info., ECF No. 285.12.)

Roscigno’s Resignation and Subsequent Employment with Liquidia

8. Roscigno resigned from UTC on 18 June 2007. (Roscigno Aff. ¶ 8.) At

the time of his resignation, Tyvaso® had not yet received FDA approval. (See Feigal

Report ¶ 79 (observing that Tyvaso® was not approved as an orphan drug until 9

April 2009).) 4

3 On 9 September 2024, Liquidia filed a Motion to Exclude the opinions of UTC’s expert, Dr. David W. Feigal (Feigal), both at summary judgment and at trial, (ECF No. 312). On 23 July 2025, the Court entered an Order granting in part the Motion and excluding certain of Feigal’s opinions. (See Order on Mot. Exclude, ECF No. 382.) While the Court cites to Feigal’s expert report throughout this Opinion, it does not rely on any excluded statements or opinions.

4 “An orphan drug is a drug intended to treat a condition affecting fewer than 200,000 persons in the US, or which will not be profitable within 7 years following approval by the FDA[.]” U.S. FOOD & DRUG ASSOCIATION, FDA/CDER SMALL BUSINESS CHRONICLES (July 13th, 9. Despite a practice of conducting exit interviews with departing

employees, UTC has no record of an exit interview with Roscigno during which it

would have requested the return of any UTC-related information. (Dep. of Alyssa

Friedrich, Individually and as Corporate Representative on Behalf of UTC [Pls.’

Friedrich Dep.] 90:8−101:22, ECF No. 255.1 (under seal), ECF No. 335.1 (public

version); Dep. of Alyssa Friedrich, Individually and as Corporate Representative on

Behalf of UTC [Def.’s Friedrich Dep.] 135:5−136:15, ECF No. 285.17 (under seal),

ECF No. 347 (public version); Memo. from A.

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