Schor v. Abbott Laboratories

378 F. Supp. 2d 850, 2005 U.S. Dist. LEXIS 14261, 2005 WL 1653606
CourtDistrict Court, N.D. Illinois
DecidedJuly 12, 2005
Docket05 C 1592
StatusPublished
Cited by4 cases

This text of 378 F. Supp. 2d 850 (Schor v. Abbott Laboratories) is published on Counsel Stack Legal Research, covering District Court, N.D. Illinois primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Schor v. Abbott Laboratories, 378 F. Supp. 2d 850, 2005 U.S. Dist. LEXIS 14261, 2005 WL 1653606 (N.D. Ill. 2005).

Opinion

MEMORANDUM OPINION AND ORDER

GETTLEMAN, District Judge.

Plaintiff Gary Schor filed a three-count class action complaint against defendant *852 Abbott Laboratories (“Abbott”), alleging violations of the Sherman Antitrust Act (“Sherman Act”), 15 U.S.C. § 2, and the Illinois Consumer Fraud Act, 815 ILCS 505/1, et seq. Plaintiff also asserts a state law claim for unjust enrichment. Plaintiff alleges that defendant used its monopoly over its patented AIDS drug Norvir to unreasonably inflate the price of competitors’ drug combinations that contain Nor-vir.

Subject matter jurisdiction of the Sherman Act claim is based on 28 U.S.C. §§ 1331 and 1337, and 15 U.S.C. § 15. Jurisdiction over the state law claims is based on supplemental jurisdiction pursuant to 28 U.S.C. § 1367.

Defendant has moved to dismiss the complaint pursuant to Fed.R.Civ.P. 12(b)(6) for failure to state a claim. For the reasons discussed below, the court grants defendant’s motion to dismiss Count I, and declines to exercise supplemental jurisdiction over the state law claims.

FACTS 1

Defendant Abbott, an Illinois corporation, is a pharmaceutical company engaged in the business of manufacturing, developing, and distributing anti-retroviral drugs worldwide, including throughout the United States. Plaintiff, a citizen of Florida, purchased one of defendant’s AIDS drugs, Norvir, for his personal use.

Norvir was originally marketed as a stand-alone protease inhibitor (“PI”). Pis are anti-retroviral drugs that inhibit the AIDS virus from copying itself into new cells. Plaintiff alleges that Norvir cannot be interchanged with any other drug, and therefore constitutes a product market subject to antitrust laws. Through various patents, defendant controls 100% of the Norvir market, and there are no generic versions of Norvir. Norvir causes severe side effects when used alone, but when taken in conjunction with other Pis, it boosts the effectiveness of the other drugs. These “boosted Pis” also remain effective for longer periods of time. It is important for AIDS patients to have a variety of Pis available to them because patients may build a tolerance to certain drug combinations.

Defendant produces its own boosted PI, called Kaletra, which is boosted by Norvir. At least seven other boosted Pis, not manufactured by defendant, are boosted by Norvir: Agenerase, Crixivan, Fortovase, Invirase, Lexiva, Reyataz, and Viracept. Plaintiff alleges that Pis boosted by Nor-vir are not interchangeable with any other drugs and are a market subject to antitrust laws. Plaintiff asserts that defendant effectively controls this market for “all of the anti-retroviral drugs dependent on a boost from Norvir in the United States,” and that the United States is a proper geographical market for antitrust purposes.

Kaletra, defendant’s boosted PI, began to lose its market share in 2003. In December 2003, defendant raised the price of Norvir by more than 400%. 'Defendant did not, however, pass this price increase on to Kaletra. As a result, Kaletra costs substantially less than other boosted Pis. Plaintiff asserts that defendant’s “anticom-petitive pricing scheme is designed to exclude competition for Kaletra, even though Kaletra might not be the most effective PI for a particular patient.” Prior to the increase, it was projected that defendant would receive over $2 billion in revenues *853 for Norvir. According to plaintiff, defendant “had no legitimate justification for the exorbitant price increase of Norvir other than to strangle the market to the detriment of AIDS victims.”

DISCUSSION

In ruling on a motion to dismiss for failure to state a claim, the court accepts the allegations of the complaint as true and views the facts in the light most favorable to the plaintiff. Travel All Over the World, 73 F.3d at 1428. A complaint should not be dismissed for failure to state a claim unless there is no doubt that the plaintiff cannot prove a set of facts that would entitled her to relief based on her claim. Pressalite Corp. v. Matsushita Electric Corp. of America, 2003 WL 1811530, at *2 (N.D.Ill. Apr.4, 2003).

I. Collateral estoppel

Plaintiff argues in his response to the motion to dismiss that defendant is collaterally estopped from raising its arguments in favor of its motion to dismiss by two earlier decisions issued by Judge Wilken of the Northern District of California, Doe v. Abbott Laboratories, C 04-1511 CW, un-pub. order (N.D.Cal. Oct. 21, 2004), and Service Employees International Union Health and Welfare Fund v. Abbott Laboratories, 2005 WL 528323 (N.D.Cal. Mar.2, 2005). Like the instant case, Doe and Service Employees are class actions against defendant brought by indirect consumers of Norvir. The Doe and Service Employee$ plaintiffs allege violations of the Sherman Act, as well as violations of the California Business and Professions Code and state law unjust enrichment claims. Judge Wilken denied the defendant’s motions to dismiss in both cases, which remain pending.

. In the instant case, defendant argues that collateral estoppel does not apply because a ruling on a motion to dismiss is not a “final judgment,” and thus does not trigger collateral estoppel. 2 Collateral estoppel, or issue preclusion, bars the litigation in a subsequent action of an issue that has been decided in a prior action. Meyer v. Rigdon, 36 F.3d 1375, 1378 n. 1 (7th Cir.1994). The Seventh Circuit has held that the party invoking collateral estoppel has the burden of proving four elements: (1) that the issue sought to be precluded is identical to the issue raised in the prior action; (2) that the issue was actually litigated; (3) that determination of the issue was essential to the final judgment; and (4) that the party against whom estoppel is invoked was fully represented in the prior action. Id. The party asserting estoppel has the burden of establishing which issues were actually determined in his favor in a prior action. Gilldorn Savings Ass’n. v. Commerce Savings Ass’n., 804 F.2d 390, 393 (7th Cir.1986).

Although defendant is correct that a ruling denying a motion to dismiss is typically not a final judgment for the purposes of collateral estoppel, the Seventh Circuit has

Free access — add to your briefcase to read the full text and ask questions with AI

Related

Louisiana Wholesale Drug Co. v. Shire LLC
929 F. Supp. 2d 256 (S.D. New York, 2013)
Schor, Gary v. Abbott Laboratories
457 F.3d 608 (Seventh Circuit, 2006)
In Re Abbott Laboratories Norvir Anti-Trust Litigation
442 F. Supp. 2d 800 (N.D. California, 2006)

Cite This Page — Counsel Stack

Bluebook (online)
378 F. Supp. 2d 850, 2005 U.S. Dist. LEXIS 14261, 2005 WL 1653606, Counsel Stack Legal Research, https://law.counselstack.com/opinion/schor-v-abbott-laboratories-ilnd-2005.