Dennis Coker, on behalf of himself and all others similarly situated v. The Purdue Pharama Company

CourtCourt of Appeals of Tennessee
DecidedNovember 30, 2006
DocketW2005-02525-COA-R3-CV
StatusPublished

This text of Dennis Coker, on behalf of himself and all others similarly situated v. The Purdue Pharama Company (Dennis Coker, on behalf of himself and all others similarly situated v. The Purdue Pharama Company) is published on Counsel Stack Legal Research, covering Court of Appeals of Tennessee primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

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Dennis Coker, on behalf of himself and all others similarly situated v. The Purdue Pharama Company, (Tenn. Ct. App. 2006).

Opinion

IN THE COURT OF APPEALS OF TENNESSEE AT JACKSON May 18, 2006 Session

DENNIS COKER, on behalf of himself and all others similarly situated, v. THE PURDUE PHARMA COMPANY, ET AL.

An Appeal from the Circuit Court for Shelby County No. CT-000121-04 Robert L. Childers, Judge

No. W2005-02525-COA-R3-CV - Filed November 30, 2006

This is a class action involving federal preemption. The defendants own a series of patents for the prescription pain medication OxyContin®. In prior separate litigation between the defendants and a generic drug manufacturer, a federal district court in New York found that the defendants committed inequitable conduct before the United States Patent Office in procuring the patents. After this order was entered by the federal court in New York, the plaintiff filed the instant class action in Shelby County, Tennessee, on behalf of all consumers of OxyContin, alleging violations of the Tennessee Trade Practices Act, the Tennessee Consumer Protection Act, and common law monopolization. These state law claims were based on the defendants’ conduct before the United States Patent Office. The defendants removed the case to the federal district court for the Western District of Tennessee. The district court remanded the case back to the Tennessee trial court, holding that the finding of inequitable conduct against the defendants by the federal court in New York operated as collateral estoppel on the issue regarding the federal patent laws. On remand, the defendants filed a motion for judgment on the pleadings based on federal preemption. The trial court granted the motion. We affirm, finding that the plaintiff’s antitrust and unfair competition claims, based on the defendants’ conduct before the Patent Office, are preempted by the federal patent laws.

Tenn. R. App. P. 3 Appeal as of Right; Judgment of the Circuit Court is Affirmed.

HOLLY M. KIRBY , J., delivered the opinion of the Court, in which ALAN E. HIGHERS, J., and DAVID R. FARMER , J., joined.

B.J. Wade, Memphis, Tennessee, and of counsel, William M. Audet, San Francisco, California, Andrew N. Friedman, Phoenix, Arizona, and Robert Shelquist, Minneapolis, Minnesota, for Plaintiff/Appellant Dennis Coker.

W. David Bridgers, Nashville, Tennessee, and Timothy C. Hester, Washington, D.C., for Defendants/Appellees The Purdue Pharma Company, et al. OPINION

Defendant/Appellees The Purdue Pharma Company, Purdue Pharma L.P., The Purdue Frederick Company, Purdue Pharmaceuticals L.P., and P.F. Laboratories, Inc. (collectively, “Purdue” or “Defendants”) are pharmaceutical companies which own a series of patents for oxycodone hydrochloride controlled release: Patent No. 5,549,912; Patent No. 5,508,042; and Patent No. 5,656,295. This product is manufactured and marketed under the brand-name OxyContin® (“OxyContin”). OxyContin is an opioid analgesic pain medication manufactured with a time-release formulation, which purportedly releases controlled amounts of oxycodone into the patient’s bloodstream over a twelve-hour period of time. Unlike immediate release formulations, OxyContin is designed to provide continuous pain relief.

In order to explain the proceedings in the trial court below regarding the instant class action, we must first outline the proceedings in separate but related litigation between Purdue and generic drug manufacturers Endo Pharmaceuticals, Inc. and Endo Pharmaceuticals Holdings, Inc., (collectively, “Endo”). Prior to the expiration of Purdue’s patents, Endo announced plans to introduce into the market a generic equivalent of OxyContin. Therefore, pursuant to the procedures set forth in the Hatch-Waxman Act, see 21 U.S.C. § 355 et seq., Endo filed an Abbreviated New Drug Application (“ANDA”) with the Food and Drug Administration. Under the Hatch-Waxman Act, the filing of an ANDA affords the first generic drug manufacturer a one hundred eighty (180) day statutory period in which to market its generic product free from competing generic manufacturers. If, however, the generic drug manufacturer seeks to market its product prior to the expiration of the “pioneer” drug owner’s patents, it must notify the owner of the pioneer drug and certify that the relevant patents are either invalid or will not be infringed by the generic version of the drug for which the ANDA was submitted. The owner of the pioneer drug, upon receiving notification, then has forty-five days in which to file suit for patent infringement.

In October 2000, Purdue timely filed a patent infringement suit against Endo in the United States District Court for the Southern District of New York. See Purdue Pharma L.P. v. Endo Pharm., Inc., Nos. 00 CIV. 8029(SHS), 01 CIV. 2109(SHS), 01 CIV. 8177(SHS), 2004 WL 26523 (S.D.N.Y. Jan. 5, 2004). Purdue alleged that Endo’s generic product infringed its patents for OxyContin. Id. at *1. In response, Endo Pharmaceuticals, Inc., counterclaimed against Purdue, seeking a declaration that the OxyContin patents were invalid and unenforceable because of Purdue’s conduct in obtaining those patents. Id. Specifically, Endo asserted that Purdue committed “inequitable conduct” before the United States Patent and Trademark Office (“PTO”) by allegedly misrepresenting the proof in support of its claim that OxyContin “reduced the dosage range and eased titration in comparison to other opioid formulations.”1 Id. at *21. Following an eleven-day bench trial, Judge Sidney H. Stein agreed with Purdue that Endo’s generic product infringed

1 A patent applicant has a duty to disclose to the PTO information it knows to be material to patentability. Purdue Pharm a L.P., 2004 W L 26523, at *20. A breach of this duty can rise to the level of “inequitable conduct,” which renders the patent unenforceable. Id. To establish that a patent is unenforceable due to inequitable conduct, a party must show by clear and convincing evidence that the patent applicant failed to disclose material information with an intent to deceive the PTO. Id.

-2- Purdue’s OxyContin patents. Judge Stein found, however, that Purdue’s patents were unenforceable because Purdue had made material and intentional misrepresentations before the PTO when it obtained the patents. Id. at *27. Based on the latter finding, Judge Stein dismissed Purdue’s patent claims and entered an injunction barring enforcement of the OxyContin patents.2 Id.

On January 12, 2004, Plaintiff/Appellant Dennis Coker (“Coker” or “Plaintiff”) filed a class action lawsuit against Purdue on behalf of himself and “all natural persons in the State of Tennessee who indirectly purchased OxyContin® manufactured by [Purdue] at any time during the period [of] December 1, 1995 to the present.” According to Purdue, Coker’s lawsuit is one of approximately seventy antitrust and unfair competition lawsuits filed against Purdue based on Judge Stein’s January 2004 decision. In his complaint, Coker sets forth three separate causes of action: violations of the Tennessee Trade Practices Act, Tenn. Code Ann. § 47-25-101 et seq.; violations of the Tennessee Consumer Protection Act, Tenn. Code Ann. § 47-18-101 et seq.; and common law monopolization. In particular, Coker alleges that Purdue established and maintained monopolies, contracts, agreements, combinations, and conspiracies in restraint of trade and commerce in the market of oxycodone hydrochloride controlled release products. As a result, Coker avers, consumers of OxyContin have paid and continue to pay artificially inflated and non-competitive prices for the pain medication.

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