Coker v. Purdue Pharma Co.

314 F. Supp. 2d 777, 32 Employee Benefits Cas. (BNA) 2332, 2004 U.S. Dist. LEXIS 6988, 2004 WL 870661
CourtDistrict Court, W.D. Tennessee
DecidedApril 23, 2004
Docket04-2145-DP
StatusPublished
Cited by4 cases

This text of 314 F. Supp. 2d 777 (Coker v. Purdue Pharma Co.) is published on Counsel Stack Legal Research, covering District Court, W.D. Tennessee primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Coker v. Purdue Pharma Co., 314 F. Supp. 2d 777, 32 Employee Benefits Cas. (BNA) 2332, 2004 U.S. Dist. LEXIS 6988, 2004 WL 870661 (W.D. Tenn. 2004).

Opinion

ORDER GRANTING MOTION TO REMAND

DONALD, District Judge.

Before the Court is the motion of Dennis Coker (“Plaintiff’) to remand this class action to the Circuit Court for Shelby County, Tennessee. The Purdue Pharma Company, Purdue Pharma L.P., The Purdue Frederick Company, Purdue Pharmaceuticals L.P., and P.F. Laboratories, Inc. (collectively “Defendants” or “Purdue”) removed the case to this Court on February 27, 2004, pursuant to 28 U.S.C. § 1441(a), arguing that original federal subject matter jurisdiction exists under 28 U.S.C. §§ 1331 and 1338. For the following reasons, the Court grants Plaintiffs motion to remand.

I. Factual and Procedural Background 1

Plaintiff is an individual citizen of Tennessee. Defendants are corporations or *779 general partnerships organized under the laws of Delaware, New York, or New Jersey. Defendants Purdue Pharma L.P., The Purdue Frederick Company, and The Purdue Pharma Company are in the business of research, development, and sale of pharmaceutical products in the United States. Defendant Purdue Pharmaceuticals L.P. is in the business of manufacturing and formulating medications for sale of pharmaceutical products in the United States. Defendant P.F. Laboratories is in the business of the production of pharmaceutical products in the United States. The named Plaintiffs damages are less than $75,000.00.

Defendants are the owners of several patents 2 for oxycodone hydrochloride controlled release, which they manufacture and market under the brand-name Oxy-Contin® (“OxyContin”). Defendants’ Oxy-Contin is one of the best selling severe pain medications in the United States, reaching sales of $1.8 billion annually. It is an opioid analgesic containing a time-release formulation, purportedly so as to release controlled amounts of oxycodone over a twelve-hour period, thus providing continuous pain relief. No generic equivalent to OxyContin is yet available in the marketplace.

In 2000, Defendants filed a patent infringement suit against Endo Pharmaceuticals Holdings Inc. and Endo Pharmaceuticals Inc. (collectively “Endo”), after Endo filed its Abbreviated New Drug Application (“ANDA”) for its generic equivalent of OxyContin. The filing of an ANDA grants the manufacturer of the first generic drug to receive approval a 180-day statutory period of market exclusivity during which time the generic drug manufacturer has the right to market its drug absent other generic competition. The generic ANDA applicant must notify the owner of the brand-name drug of the filing of its ANDA and certify, when appropriate, that the patents covering the brand-name drug are either invalid or not infringed by the generic version. The brand-name drug owner need only file a patent infringement lawsuit within forty-five days so as to block the ANDA applicant’s generic drug from entering the market for up to thirty months.

After a non-jury trial, Judge Stein of the United States District Court for the Southern District of New York held that Endo’s ANDA infringed Purdue’s patents for Oxy-Contin, but that Purdue’s inequitable conduct before the United States Patent and Trademark Office (“PTO”) during prosecution of the OxyContin patents rendered those patents unenforceable. Specifically, Judge Stein found, by clear and convincing evidence, that Purdue committed an intentional misrepresentation in failing to disclose material information inconsistent with its assertions that it had “surprisingly discovered” that its invention reduced the dosage range and eased titration in comparison to other opioid formulations. See Purdue Pharma L.P. v. Endo Pharm. Inc., No. 00 CIV 8029(SHS), slip op. at *20-*27, 2004 WL 257753 (S.D.N.Y. Jan. 5, 2004). This ruling is now on appeal to the U.S. Court of Appeals for the Federal Circuit.

On January 12, 2004, Plaintiff filed a complaint in the Circuit Court for Shelby County, Tennessee. Plaintiff brings this case on behalf of a purported class of “all natural persons in the State of Tennessee who indirectly purchased OxyContin® manufactured by Defendants at any time during the period December 1, 1995 to the present.” (Comply 15.) Plaintiff alleges that Defendants established and main *780 tained monopolies, contracts, agreements, combinations, and conspiracies in restraint of trade in the market for OxyContin. Plaintiff further avers that Defendants unlawfully attempted to obtain and enforce such a monopoly through material misrepresentations to the PTO and through sham litigation against potential producers of any generic equivalent of the drug. Plaintiff alleges (1) violations of the Tennessee Trade Practices Act, Tenn.Code Ann. § 47-25-101 et seq.; (2) violations of the Tennessee Consumer Protection Act, Tenn.Code Ann. § 47-18-101 et seq.; and (3) common law monopolization.

Defendants removed to this Court on February 27, 2004, arguing as their basis for removal that, while Plaintiff purports to bring only state law causes of action, federal jurisdiction exists based on (1) a substantial federal question as a necessary element of the state claims and (2) complete preemption of the state claims by the Employee Retirement Income Security Act of 1974, 29 U.S.C. § 1001 et seq. (“ERISA”). Plaintiff filed a motion to remand on March 12, 2004, and Defendants responded on March 30, 2004. Plaintiff replied on April 19, 2004.

This case is one of fifty-two antitrust lawsuits filed against Purdue based on its litigation against Endo in the Southern District of New York. These lawsuits all make essentially the same contentions: that Defendants’ patent litigation against Endo was a “sham” and that Defendants used improper conduct in prosecuting their patents. Nineteen of the cases were brought in state courts, and Purdue removed all of those. Twenty-seven of the cases are pending in the Southern District of New York, and Purdue seeks transfer of the remaining cases to that district as well. Defendants’ motion to transfer this case to the Southern District of New York is currently pending before this Court. 3

II. Removal Standard

A defendant may remove a civil case over which the United States district courts would have original jurisdiction. See 28 U.S.C. § 1441(a) (2004). If this Court determines that it would not have had original subject matter jurisdiction over the case, it must remand to state court. See 28 U.S.C. § 1447 (2004).

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314 F. Supp. 2d 777, 32 Employee Benefits Cas. (BNA) 2332, 2004 U.S. Dist. LEXIS 6988, 2004 WL 870661, Counsel Stack Legal Research, https://law.counselstack.com/opinion/coker-v-purdue-pharma-co-tnwd-2004.