Ieradi v. Mylan Laboratories, Inc.

230 F.3d 594, 2000 WL 1207267
CourtCourt of Appeals for the Third Circuit
DecidedAugust 25, 2000
Docket00-3076
StatusUnknown
Cited by3 cases

This text of 230 F.3d 594 (Ieradi v. Mylan Laboratories, Inc.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Third Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Ieradi v. Mylan Laboratories, Inc., 230 F.3d 594, 2000 WL 1207267 (3d Cir. 2000).

Opinion

OPINION OF THE COURT

ROSENN, Circuit Judge.

In this'time of rapidly escalating prices of branded and generic drugs, the primary question on this appeal pertains to the adverse impact of such prices not on the consumer public, but rather on potential stockholders of a leading drug manufactur *596 er. Plaintiff Frank P. Ieradi purchased common stock in defendant Mylan Laboratories, Inc. (Mylan), in the face of a price investigation being conducted by the Federal Trade Commission (FTC). The investigation, which focused on Mylan’s recent increases in the prices of fourteen of its drugs, ultimately resulted in the FTC filing a complaint in federal district court alleging that Mylan had engaged in practices in restraint of trade in violation of the Sherman Act. The plaintiff alleges that initiation of the action by the FTC, in turn, caused Mylan’s stock price to drop over three points.

Following this drop in stock price, Ieradi filed a complaint in the United States District Court for the Western District of Pennsylvania claiming that Mylan violated section 10(b) of the Securities and Exchange Act of 1934 (the 1934 Act) and Securities and Exchange Commission Rule 10b-5 by concealing, in both its press releases and filings with the Securities and Exchange Commission (SEC), the existence of two supply contracts which gave Mylan exclusive access to raw materials necessary to produce two of its generic anti-anxiety medications. These exclusive contracts enabled Mylan to obtain higher prices for drugs and presumably greater profits for its stockholders. The complaint also charges that the individual officers and directors of Mylan are liable for its misconduct because they are control persons within the meaning of section 20 of the 1934 Act. The District Court dismissed Ieradi’s complaint, holding that disclosure of the exclusive supply contracts would not have significantly altered the total mix of information available to the reasonable investor, and that therefore the failure to disclose specifically those contracts was not material. Ieradi timely appealed and we affirm. 1

I.

Mylan manufactures and markets generic pharmaceuticals, including two anti-anxiety medications named lorazepam and chlorazepate. The raw materials essential to the manufacture of these two drugs are produced solely by Profarmaco S.r.l. (“Pro-farmaco”), an Italian company, and distributed in the United States solely by Gyma Laboratories of America (“Gyma”). In November of 1997, Mylan entered into agreements with Profarmaco and Gyma that gave it exclusive access to these raw materials in the United States for a period of ten years.

Shortly after entering the agreements, Mylan raised its prices significantly on fourteen generic drugs, including lorazep-am and chlorazepate. On January 12, 1998, Mylan increased the price of chlo-razepate tablets by amounts ranging from 1900% to 3200%. On March 3, 1998, My-lan raised its prices on lorazepam tablets. These increases ranged from 1900% to 2600%. Mylan made the increases, although the cost of manufacturing both clo-razepam and lorazepate remained steady.

On February 17, 1998, Mylan filed its Form 10-Q with the SEC for the quarter ending December 31, 1997. In this 10-Q, Mylan reported on the existence of an exclusive supply and distribution agreement it had entered into with a Canadian company, Genpharm, Inc., relating to the sale of another drug in the United States. The report, however, mentioned nothing about the exclusive contracts with Profar-maco and Gyma.

On June 19, 1998, Mylan filed its Form 10-K with the SEC for the fiscal year ending March 31, 1998. In that filing, the company stated:

While Mylan anticipates continued benefits from price increases in the near future, the continuation of this trend and any resulting benefits depend on several *597 factors, some of which are beyond the Company’s control.

The Form 10-K also reported increases in Mylan’s revenues and net earnings of 37% and 132%, respectively.

On July 4, 1998, Mylan filed its Form 10-Q with the SEC for the quarter ending June 30, 1998. The 10-Q reported similar increases with respect to revenues and earnings, attributing the significant earnings improvements to overall shipment volumes and selective price increases on fourteen products implemented during the June 1998 quarter. The 10-Q then disclosed the existence of an investigation by the Federal Trade Commission (“PTC”).

Specifically, the 10-Q stated:
As a result of price increases initiated by the Company during the past six months, the Company has received notification from the Federal Trade Commission that it is investigating whether the Company and others have engaged in activities restricting competition in the manufacture or sale of pharmaceutical ingredients or products. The Company is cooperating fully with the review and is providing all the information requested by the Commission. As with all governmental inquiries the process is inherently uncertain.

The 10-Q further reported:

While these price increases have favorably impacted earnings in the current quarter, the extent if any in future quarters depends upon several factors, some of which are beyond the Company’s control. During the quarter ended June 30, 1998, the Company received notice that the Federal Trade Commission , in light of the price increases, was investigating whether the Company and others had engaged in activities restricting competition in the manufacture or sale of pharmaceutical ingredients or products. The Company is cooperating fully with this investigation and is supplying the documents requested. Management believes that the Company has acted properly and in full compliance with the Federal Trade Commission Act and all other laws and regulations governing trade and competition in the marketplace.'. .. The Company believes the ultimate resolution of this matter will not have a material adverse effect on the Company’s financial position or results of operations.

In the “Forward Looking Statements” section of the same 10-Q, Mylan stated:

The Company may be unable to realize [its] plans and objectives ... due to various important factors, including, but not limited to, ... if the FTC concludes, on the basis of its investigation, that the Company has acted improperly.

On July 6, 1998, the Wall Street Journal reported on Mylan’s price increases on the fourteen drugs, including lorazepam and chlorazepate. Around that time, a Mylan spokesperson specifically denied that My-lan had cornered the market on certain raw materials needed to manufacture these two anti-anxiety medications. However, on or about July 20,1998, Mylan Vice President Patricia Sunseri revealed that the FTC had sent a subpoena to the company the previous month asking about a series of price increases on generic drugs since the prior fall. Sunseri claimed the FTC “just wanted to make sure ... [the price increases] w[ere] justified.” Still, Mylan made no public reference at this time to its contracts with Profarmaco and Gyma.

On October 26, 1998, Ieradi purchased 100 shares of Mylan stock at a price of $33-13/16.

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230 F.3d 594, 2000 WL 1207267, Counsel Stack Legal Research, https://law.counselstack.com/opinion/ieradi-v-mylan-laboratories-inc-ca3-2000.