Classen Immunotherapies, Inc. v. King Pharmaceuticals, Inc.

466 F. Supp. 2d 621, 2006 U.S. Dist. LEXIS 90806, 2006 WL 3716920
CourtDistrict Court, D. Maryland
DecidedAugust 16, 2006
DocketCIV. WDQ-04-3521
StatusPublished
Cited by3 cases

This text of 466 F. Supp. 2d 621 (Classen Immunotherapies, Inc. v. King Pharmaceuticals, Inc.) 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
Classen Immunotherapies, Inc. v. King Pharmaceuticals, Inc., 466 F. Supp. 2d 621, 2006 U.S. Dist. LEXIS 90806, 2006 WL 3716920 (D. Md. 2006).

Opinion

Memorandum Opinion

QUARLES, District Judge.

Classen Immunotherapies, Inc. (“Classen”) has sued Elan Corporation, PLC, and Elan Pharmaceuticals, Inc. (“Elan”) for patent infringement. Elan has counterclaimed alleging noninfringement, unenforceability of Classen’s patents, defamation, false light invasion of privacy and unfair competition. Pending are Elan’s motions for summary judgment, for clarification, to seal, and for discovery. Also pending is Classen’s motion for partial summary judgment. For the following reasons, Elan’s motion for summary judgment, for clarification, and to seal will be granted. Elan’s motion for discovery and Classen’s motion for partial summary judgment will be denied.

I. Background

Classen Immunotherapies, Inc. (“Classen”) is a Maryland corporation that has developed and patented methods for identifying and commercializing new uses of existing drugs. Complaint, p. 1. Classen is the holder of Patents 6,219,674 Bl, “System for Creating and Managing Proprietary Product Data” (the “674 patent”), and 6,584,472 B2, “Method, System and Article for Creating and Managing Proprietary Product Data” (the “472 patent”). Id.

Elan is an Irish pharmaceutical company. Until 2003, Elan produced Skelaxin, a muscle relaxant.

In 2001, Elan learned of a study, conducted by a generic drug manufacturer, that indicated that Skelaxin’s rate of absorption differed inside and outside the *624 body. Elan conducted its own study in July 2001, and found that food had a significant impact on Skelaxin’s bioavailability. Browning Deck, Ex. 1. Based on these findings, Elan submitted a Citizen Petition to the FDA requesting that the FDA require drug manufacturers seeking approval of generic forms of Skelaxin to submit fed and fasted studies in Abbreviated New Drug Applications (“ANDA”). Elan also submitted a labeling supplement to its own New Drug Application (“NDA”) 1 for Skelaxin that included the results of the study. Id at Ex. 3.

The FDA granted Elan’s request for a requirement of fed and fasted studies for all generic Skelaxin ANDAs and approved Elan’s amendments to the Skelaxin product label. Browning Deck, Ex. 2,3. Elan was also ultimately granted patent numbers 6,407,128 and 6,683,102 on the relabeled Skelaxin. Goldman Decl, ¶ 4.

Classen alleges that Elan infringed the 472 and 674 patents when it: 1) studied the effect of food on the bioavailability of Skelaxin; 2) used the study data to identify a new use of the drug; and 3) commercialized the new use. Plaintiffs First Supplemental Response to Defendant Elan Pharmaceuticals Interrogatory No. 3. Elan has moved for summary judgment on Classen’s claims.

Elan has counterclaimed, arguing that Elan did not infringe Classen’s patents, the patents are unenforceable, and that Classen defamed Elan, invaded its privacy and damaged its business by issuing a false press statement and by claiming that Elan and Classen had an ongoing business relationship. Classen has moved for summary judgment on Elan’s defamation, invasion of privacy and damage to business claims.

II. Elan’s Motion for Summary Judgment

Under Rule 56(c), summary judgment is appropriate when there is no genuine issue of material fact, and the moving party is entitled to judgment as a matter of law. Celotex Corp. v. Catrett, 477 U.S. 317, 322, 106 S.Ct. 2548, 91 L.Ed.2d 265 (1986). A dispute about a material fact is genuine “if the evidence is such that a reasonable jury could return a verdict for the nonmoving party.” Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 248, 106 S.Ct. 2505, 91 L.Ed.2d 202 (1986). In considering a motion for summary judgment, “the judge’s function is not ... to weigh the evidence and determine the truth of the matter but to determine whether there is a genuine issue for trial.” Id. at 249, 106 S.Ct. 2505. Thus, “the judge must ask ... whether a fair-minded jury could return a verdict for the [nonmoving party] on the evidence presented.” Id. at 252, 106 S.Ct. 2505.

The court must view the facts and reasonable inferences drawn therefrom “in the light most favorable to the party opposing the motion.” Matsushita Elec. Indus. Co. v. Zenith Radio Corp., 475 U.S. 574, 587, 106 S.Ct. 1348, 89 L.Ed.2d 538 (1986). However, the opposing party must produce evidence upon which a reasonable fact finder could rely. Celotex Corp. v. Catrett, 477 U.S. 317, 106 S.Ct. 2548, 91 L.Ed.2d 265 (1986). The mere existence of a “scintilla” of evidence is insufficient to preclude summary judgment. Anderson, 477 U.S. at 252, 106 S.Ct. 2505.

Elan has moved for summary judgment arguing that even if its conduct fell within the scope of the 674 and 472 patents (which it does not concede), it is immune from patent enforcement under the “safe harbor” provision of the Patent Act, 35 U.S.C. § 271(e)(1), because the results of *625 its research were submitted to the Food and Drug Administration (“FDA”). Classen argues in response that § 271(e)(1) is inapplicable to the patents and the conduct in question.

Under § 271, “whoever without authority makes, uses, offers to sell, or sells any patented invention.. .infringes the patent.” 35 U.S.C. § 271(a). Section 271(e)(1), however, provides that:

[i]t shall not be an act of infringement to make, use, offer to sell or sell... a patented invention... solely for uses reasonably related to the development and submission of information under a federal law which regulates the manufacture, use or sale of drugs....

35 U.S.C. § 271(e)(1).

The Supreme Court has interpreted § 271(e)(1) broadly, holding that the provision “extends to all uses of patented inventions that are reasonably related to the development and submission of any information under the FDCA.” Merck KGaA v. Integra Lifesciences I, Ltd., 545 U.S. 193, 125 S.Ct. 2372, 2380, 162 L.Ed.2d 160 (2005)(emphasis in the original). According to the Court, “there is simply no room in the statute for excluding certain information from the exemption on the basis of the phase of research in which it is developed or the particular submission in which it could be included.” Id.

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Bluebook (online)
466 F. Supp. 2d 621, 2006 U.S. Dist. LEXIS 90806, 2006 WL 3716920, Counsel Stack Legal Research, https://law.counselstack.com/opinion/classen-immunotherapies-inc-v-king-pharmaceuticals-inc-mdd-2006.