Currax Pharmaceuticals LLC v. OptiNose AS

CourtCourt of Chancery of Delaware
DecidedJanuary 22, 2021
DocketC.A. No. 2020-0122-MTZ
StatusPublished

This text of Currax Pharmaceuticals LLC v. OptiNose AS (Currax Pharmaceuticals LLC v. OptiNose AS) is published on Counsel Stack Legal Research, covering Court of Chancery of Delaware primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Currax Pharmaceuticals LLC v. OptiNose AS, (Del. Ct. App. 2021).

Opinion

IN THE COURT OF CHANCERY OF THE STATE OF DELAWARE

CURRAX PHARMACEUTICALS LLC, ) ) Plaintiff, ) ) v. ) C.A. No. 2020-0122-MTZ ) OPTINOSE AS and ) OPTINOSE, INC, ) ) Defendants. )

MEMORANDUM OPINION Date Submitted: October 23, 2020 Date Decided: January 22, 2021

Daniel A. O’Brien, VENABLE LLP, Wilmington, Delaware; Christopher P. Borello, Joshua D. Calabro, VENABLE LLP, New York, New York; Attorneys for Plaintiff Currax Pharmaceuticals LLC.

Daniel M. Silver, Benjamin A. Smyth, MCCARTER & ENGLISH, LLP, Wilmington, Delaware; Timothy P. McAnulty, Cara E. Regan, FINNEGAN, HENDERSON, FARABOW, GARRETT & DUNNER, LLP, Washington, D.C.; Attorneys for Defendants OptiNose AS and OptiNose, Inc.

ZURN, Vice Chancellor. Cross motions for judgment on the pleadings present the Court with

competing interpretations of a patent licensing agreement. That agreement grants

the licensee an exclusive license in the licensor’s patents to make and sell a certain

drug in the United States, Canada, and Mexico. The agreement also divides control

of the subject patents’ prosecution. While the licensor retained the sole right to

prosecute its “Platform Patents,” the licensee gained the first right to prosecute the

“Product Patents” subject to certain limitations and approval rights in favor of the

licensor. The licensor also agreed to affirmatively transfer prosecution rights to the

licensee. The parties disagree about the scope of the licensee’s prosecution rights,

what the licensor must do to “transfer” those rights, and the scope of the licensor’s

approval rights.

This dispute is inspired by the licensee’s quest to file a terminal disclaimer on

a Product Patent over another Product Patent, for which the licensee controls

prosecution. The licensee has thus far been unable to file that terminal disclaimer

because its limited authority before the United States Patent and Trademark Office,

granted via an Authorization to Act, does not permit it to make that filing. The

licensee cannot file its proposed terminal disclaimer without a power of attorney.

To remedy this deficiency, the licensee seeks a power of attorney over the Product

Patents from the licensor. The licensee argues that such a power of attorney is

necessary to effectuate its prosecution rights. The licensor has refused, maintaining

1 that it has no such obligation under the agreement. The licensee brought this action

seeking an order for specific performance requiring the licensor to grant the power

of attorney.

This opinion concludes that the licensee’s “prosecution” powers permit it to

file terminal disclaimers, and that by agreeing to cooperate in transferring

prosecution rights to the licensee, the licensor agreed to execute the power of

attorney required for the licensee to implement those rights. Moreover, the

licensor’s approval rights do not reach filing a terminal disclaimer on a Product

Patent over a Product Patent. For the reasons that follow, the licensee’s motion is

granted, and the licensor’s motion is denied.

I. BACKGROUND1

Defendants OptiNose AS and OptiNose, Inc. (together, “OptiNose” or

“Defendants”) develop pharmaceutical products.2 Among these products is a

sumatriptan nasal powder known as ONZETRA® XSAIL® (“Onzetra”). Onzetra

provides a 22mg dose, dry powder formulation of sumatriptan, administered via a

1 On the parties’ cross motions for judgment on the pleadings, I draw all facts from the pleadings and documents integral to them. Citations in the form of “Compl. ¶ ––” refer to the plaintiff’s complaint, available at Docket Item (“D.I.”) 1. Citations in the form of “Answer ¶ ––” refer to the defendants’ answer to the complaint, and citations in the form “Countercl. ¶ ––” refer to defendants’ counterclaims; both are available at D.I. 11. Citations in the form “Countercl. Answer ¶ ––” refer to plaintiff’s answer to defendants’ counterclaims, available at D.I. 17. Citations in the form of “Hrg. Tr. ––” refer to the transcript of the October 23, 2020 hearing on the motions, available at D.I. 50. 2 OptiNose, AS is OptiNose, Inc.’s wholly-owned Norwegian subsidiary.

2 breath powered exhalation delivery system. It is approved by the Food and Drug

Administration for the acute treatment of migraine headaches in adults.

On September 25, 2019, OptiNose and Plaintiff Currax Pharmaceuticals LLC

(“Currax” or “Plaintiff”) entered into a licensing agreement (the “Agreement”).3

The Agreement gives Currax an exclusive license to, among other things,

manufacture and sell Onzetra in the United States, Canada, and Mexico.4 The

Agreement divides OptiNose’s patents embodied in Onzetra into “Product Patents”

and “Platform Patents.”5 Currax acquired the first right to control prosecution of the

“Product Patents,”6 while OptiNose retained prosecution control over the “Platform

Patents.”7

Section 5.01(a)(i) of the Agreement describes Currax’s prosecution rights for

Product Patents:

3 See Compl. Ex. A. [hereinafter “Agr.”]. 4 See id. § 2.01(a)(i). 5 The term “OptiNose Patents” is defined to include the patents listed in Schedule 1.01(b). See id. § 1.01(defining “OptiNose Patents”). Schedule 1.01(b) includes a list of patents that OptiNose controls and that are necessary to, among other things, make, sell, and import the Onzetra. See id. Sched. 1.01(b); see also id. § 6.02(a). 6 See id. § 5.01(a)(i); see also id. Sched. 1.01(d) (listing the Product Patents). 7 See id. § 5.01(a)(ii); see also id. Sched. 1.01(c) (listing the Platform Patents).

3 Currax shall have the first right to control the Prosecution and maintenance of the Product Patents in the Territory; provided that Currax shall provide copies to OptiNose of all communications with the applicable patent offices reasonably in advance of filing and OptiNose shall have the right to review and comment on such filings, which Currax shall reasonably consider; provided, further, that filings or statements in any filing relating to or characterizing the Device component of the Product or other OptiNose intellectual property shall require OptiNose’s prior approval (such approval not to be unreasonably withheld, conditioned or delayed). If Currax determines to abandon or not maintain any Product Patent, then Currax shall notify OptiNose of such determination sufficiently in advance of any filing or response deadline (and in any event at least thirty (30) days in advance) and OptiNose shall then have the right (but not the obligation) to Prosecute and maintain such Product Patent in OptiNose’s name, and the licenses granted to Currax set forth in Section 2.01(a)(i) will be terminated with respect to such Product Patent. If a Product Patent issues with claims that are listable for or Cover XHANCE® (fluticasone propionate), such Patent shall cease to be a Product Patent and shall thereafter be a Platform Patent. In such instance, Currax shall take actions in accordance with Section 5.01(c) to transfer Prosecution and maintenance of such Patent(s) to OptiNose.8

“Prosecution” as defined in the Agreement includes any ex parte proceeding before

the United States Patent and Trademark Office (“USPTO”):

“Prosecution” means, with respect to the Territory, any ex parte procedure or practice before an administrative agency such as the [USPTO], or an equivalent agency, including but not limited to filing patent applications, prosecuting patent claims, reexaminations, reissues and the like. For the avoidance of doubt, Prosecution does not include post-grant reviews, inter partes reviews or oppositions.9

8 Id. § 5.01(a)(i) (emphasis in original). 9 Id.

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