AZURITY PHARMACEUTICALS, INC. v. AMNEAL PHARMACEUTICALS LLC

CourtDistrict Court, D. New Jersey
DecidedAugust 25, 2022
Docket3:21-cv-08717
StatusUnknown

This text of AZURITY PHARMACEUTICALS, INC. v. AMNEAL PHARMACEUTICALS LLC (AZURITY PHARMACEUTICALS, INC. v. AMNEAL PHARMACEUTICALS LLC) is published on Counsel Stack Legal Research, covering District Court, D. New Jersey primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
AZURITY PHARMACEUTICALS, INC. v. AMNEAL PHARMACEUTICALS LLC, (D.N.J. 2022).

Opinion

UNITED STATES DISTRICT COURT DISTRICT OF NEW JERSEY

NOT FOR PUBLICATION

AZURITY PHARMACEUTICALS, INC., Plaintiff, Civ. No. 21-08717 (GC) v. CLAIM CONSTRUCTION OPINION AMNEAL PHARMACEUTICALS, LLC, AND ORDER Defendant.

CASTNER, District Judge THIS MATTER comes before the Court on the Joint Claim Construction and Prehearing Statement regarding U.S. Patent No. 10,799,453 (“the 453 Patent”) submitted by Plaintiff Azurity Pharmaceuticals, Inc. (“Azurity”) and Defendant Amneal Pharmaceuticals LLC (“Amneal’) pursuant to L. Pat. R. 4.3. (ECF No. 55.) On January 13, 2022, Azurity and Amneal filed opening briefs. (ECF Nos. 56, 57.) On March 18, 2022, Azurity and Amneal filed response briefs, (ECF Nos, 63, 64.) On March 18, 2022, Amneal also filed a Motion to Strike the Declaration of Dr. Steven Little. (ECF No. 65.) The parties dispute whether a list of steps in claim 1 of the ’453 Patent, indicated by roman numerals (i), (ii), and (iii) — needs to be performed in the order listed. (Joint Prehr’g Stmt., Ex. A, ECF No. 55.) On June 8, 2022, pursuant to L. Pat. R. 4.6, the Court held a Markman hearing to construe the claim term. This claim term is construed below.

I. BACKGROUND A. Procedural Background This case arises out of Amneal’s filing of an Abbreviated New Drug Application (“ANDA”) with the Food and Drug Administration (“FDA”) to seek approval to market a generic version of the pharmaceutical product Katerzia®. (Joint Prehr’g Stmt. 2.) Katerzia®, a brand name pharmaceutical drug, is an oral, liquid formulation of amlodipine used to treat hypertension and coronary artery disease. (See Compl. f{ 1, 7, ECF No. 1.) Azurity, which holds the New Drug Application (“NDA”) for Katerzia®, alleges that Amneal’s ANDA infringes on four patents, including the °453 Patent, that cover Azurity’s Katerzia® product. Ud. J@ 8, 25-28.) To market and sell Katerzia®, Azurity listed the ’453 Patent in the FDA’s Approved Drug Products with Therapeutic Equivalence Applications, commonly known as the Orange Book. See 21 U.S.C. § 355(b)(1), (c)(2). Thereafter, Amneal filed its ANDA with the FDA to seek approval to market a generic version of Katerzia®. See 21 U.S.C. § 355q)(1). Accordingly, pursuant to 21 ULS.C. §§ 355qQ)(6)(B)Gii), Azurity initiated this suit against Amneal because Amneal’s request to market the generic version of Katerzia® was done prior to the expiration of the °453 Patent. (Compl. | 25.) B. The '453 Patent The ’453 Patent is the only patent at issue in this claim construction. (Joint Prehr’g Stmt. 3.)! The ’453 Patent was filed on April 11, 2019 as Application No. 16/381,575. (See U.S. Patent No. 10,799,453 (filed Apr. 11, 2019), ECF No. 1-2.) The °453 Patent is entitled “Amlodipine Formulations.” Cd. col. 11. 1.) Amlodipine is a “calcium channel blocker,” which means that it

' The other patents are United States Patent Nos. 10,695,329, 10,894,039, and 10,952,998. (Compl. 7 1.)

“affects the movement of calcium into the cells of the heart and blood vessels” and thus, “relaxes blood vessels and increases the supply of blood and oxygen to the heart while reducing its workload.” (Ud. col. i 1. 37-41.) The *453 Patent is directed to the formulation of a liquid form of amlodipine. (See id. col. 171, 24--25,) Historically, amlodipine was administered in tablet form, but the liquid formulations of amlodipine are “advantageous over conventional solid dosage administration of amlodipine ranging from ease of administration, accuracy of dosing, accessibility to additional patient populations such as to children and the elderly, and an increased patient compliance to medication.” Cd. col. 17 L. 27-32.) Cc. Claim One Claim 1 contains the only disputed claim term in this claim construction dispute. (PL.’s Opening Br. 1, ECF No. 56; Def.’s Opening Br, 1, ECF No. 57.7 Claim 1 of the °453 Patent claims the following: A suspension comprising particles comprising amlodipine benzoate and having a median diameter D50 value of between about Sum and about 40 um as measured by a light scattering particle size analyzer, and the said suspension is made by a process comprising: (i) providing an aqueous mixture comprising amlodipine besylate; (ii) adding sodium benzoate to the aqueous mixture to form a first mixture; and (iii) subjecting the first mixture fo ultrasonic agitation at a frequency of between about 20 kHz and about 100 kHz, thereby forming a second mixture comprising amlodipine benzoate, Patent col. 77 1. 44-56.)

? The parties agree that the disputed claim term and corresponding claim “include all asserted claims that depend directly or indirectly from the listed claim.” Goint Prehr’g Stmt., Ex. A A-1 n3,

The parties dispute whether the steps listed in claim 1 of the ’453 Patent must be performed in the order in which they appear in claim 1. The parties assert the following proposed claim construction:

Proposed Construction Amneal’s Steps (i), (ii), and (iii) must be performed in the order recited. Construction IL. LEGAL STANDARD The meaning and scope of patent claims are questions of law to be decided by the court. Markman yv. Westview Instruments, Inc., 517 U.S, 370, 372 (1996), “It is a bedrock principle of patent law that the claims of a patent define the invention to which the patentee is entitled the right to exclude.” Phillips v. AWH Corp., 415 F.3d 1303, 1312 (Fed, Cir, 2005) (internal citation and quotation marks omitted). “[T]here is no magic formula or catechism for conducting claim construction.” /d. at 1324, Instead, the Court is free to attach the appropriate weight to appropriate sources “in light of the statutes and policies that inform patent law.” Jd. (citing Vitronics Corp. v. Conceptronic, Inc., 90 F.3d 1576, 1582 (Fed, Cir, 1996)). “Claim construction begins with the intrinsic evidence of the patent—the claims, the specification, and the prosecution history—and may require consultation of extrinsic evidence to understand the state of the art during the relevant time period.” Merck Sharp & Dohme Corp. v. Teva Pharms, USA, Inc., 2019 WL 943532, at *2 (D.N.J. Feb. 26, 2019); see also Phillips, 415 F.3d at 1314-17. First, the court “looks to the words of the claims themselves, both asserted and nonasserted, to define the scope of the patented invention.” Vitronics Corp., 90 F.3d at 1582. The “words of a claim ‘are generally given their ordinary and customary meaning,’” which is “the meaning that the term would have to a person of ordinary skill in the art in question at the time of the invention, i.e.,

as of the effective filing date of the patent application.” Phillips, 415 F.3d. at 1312-13 (quoting Vitronics Corp., 90 F.3d at 1582). A person of ordinary skill in the art “(POSA”) “is deemed to read the claim term not only in the context of the particular claim in which the disputed term appears, but in the context of the entire patent, including the specification.” Jd, at 1313 (citing Multiform Desiecants, Inc. v. Medzam, Ltd. , 133 F.3d 1473, 1477 (Fed, Cir, 1998)), Accordingly, “the claims themselves provide substantial guidance as to the meaning of particular claim terms,” and a court may look to “the context in which a term is used in the asserted claim” and “other claims of the patent in question, both asserted and unasserted,” See id. at 1314. Second, the specification is “always highly relevant to the claim construction analysis.

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AZURITY PHARMACEUTICALS, INC. v. AMNEAL PHARMACEUTICALS LLC, Counsel Stack Legal Research, https://law.counselstack.com/opinion/azurity-pharmaceuticals-inc-v-amneal-pharmaceuticals-llc-njd-2022.