Mylan Laboratories Inc. v. American Motorists Insurance

700 S.E.2d 518, 226 W. Va. 307, 2010 W. Va. LEXIS 74
CourtWest Virginia Supreme Court
DecidedJune 18, 2010
Docket34402
StatusPublished
Cited by20 cases

This text of 700 S.E.2d 518 (Mylan Laboratories Inc. v. American Motorists Insurance) is published on Counsel Stack Legal Research, covering West Virginia Supreme Court primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Mylan Laboratories Inc. v. American Motorists Insurance, 700 S.E.2d 518, 226 W. Va. 307, 2010 W. Va. LEXIS 74 (W. Va. 2010).

Opinion

PER CURIAM:

The appellants herein, Mylan Laboratories Inc., Mylan Pharmaceuticals Inc., and UDL Laboratories Inc. (hereinafter collectively referred to as “Mylan”), appeal the February 8, 2007 order of the Circuit Court of Monongalia County that held that the appellee insurance companies, American Motorists Insurance Co., Continental Insurance Co., Wausau Insurance Co., and Federal Insurance Co., have no duty to defend Mylan in certain civil actions brought against it. Ater careful consideration of the record, the parties’ arguments, and the applicable law, this Court affirms the circuit court’s order.

I.

FACTS

Mylan, a manufacturer of generic drags, was named a defendant in lawsuits brought in several states. These lawsuits can be divided into two classes: average wholesale price litigation (hereinafter referred to as “AWP” litigation), and Lorazepam and Clorazepate litigation (hereinafter referred to as “L & C” litigation).

The AWP litigation relates to the average wholesale price of prescription drugs manufactured, marketed, and sold by Mylan. Basically, physicians and other providers of drugs are reimbursed by Medicare and other third-party payors based on the average wholesale price of the drug. Manufacturers periodically report the average wholesale price of drugs to publishers who list the prices as reported to them by the manufacturers.

The AWP litigation alleges that Mylan and others engaged in a scheme to fraudulently manipulate the average wholesale price of its drugs. As part of this scheme, Mylan reported inflated average wholesale drug prices which materially misrepresented the actual prices paid to Mylan for prescription drugs by drug providers such as hospitals, pharmacies, and physicians. As a result, drug providers were reimbursed significantly more money than they actually paid for Mylanmanufactured drugs. Moreover, Mylan used this scheme as a marketing ploy. Specifically, Mylan advertised the difference or “spread” in prices as a reason why those in the distribution chain should sell its drags, a practice known as “marketing the spread.” In this way, Mylan increased its share of the generic drug market.

The plaintiffs in the AWP cases are patients who were prescribed Mylan-manufactured drugs, third-party payors, states, and counties responsible for reimbursing drag providers based on the reported average wholesale price of Mylan-manufactured drugs. 1 As of the date of the oral argument *311 of this case before this Court, the AWP litigation was pending.

The second class of lawsuits in which Mylan was involved was the L & C litigation. These lawsuits originally were brought by the Federal Trade Commission based on alleged antitrust violations of Section 5(a) of the Federal Trade Commission Act. This litigation alleges that Mylan acquired an exclusive licensing agreement with the company which supplied the active pharmaceutical ingredients for two generic drugs manufactured by Mylan: Lorazepam and Clorazepate. The exclusive agreements prohibited the suppliers from selling these active pharmaceutical ingredients to any other generic drug manufacturer for a period of 10 years. Despite no significant increase in costs, the price charged by Mylan for Lorazepam and Clorazepate increased dramatically. Depending upon the size of the bottle, the price for Clorazepate increased by amounts ranging from 1,900 percent to 3,200 percent. 2 The price for Lorazepam tablets increased 1,900 percent to 2,600 percent. 3

The Federal Trade Commission litigation alleged eight causes of action against Mylan: (1) agreement in restraint of trade on Lorazepam; (2) agreement in restraint of trade on Clorazepate; (3) conspiracy to monopolize generic Lorazepam tablets market; (4) conspiracy to monopolize generic Clorazepate tablets market; (5) monopolization of generic Lorazepam tablets market; (6) attempted monopolization of generic Lorazepam tablets market; (7) monopolization of generic Clorazepate tablets market; and (8) attempted monopolization of generic Clorazepate tablets market. The original Federal Trade Commission complaint alleged in part that,

As a result of these substantial and unprecedented price increases for lorazepam and clorazepate tablets, many purchasers, including pharmacies, hospitals, insurers, managed care organizations, wholesalers, government agencies, and others, have paid substantially higher prices. Moreover, some patients have stopped taking lorazepam and clorazepate tablets altogether, or been forced to reduce the quantity they take, because they can not afford them.

Subsequently, thirty-two states jointly filed suit against Mylan and other defendants in a suite alleging violations of each state’s antitrust laws. Several third-party payors filed similar actions against Mylan. A global settlement was reached in most of these cases wherein Mylan agreed to pay over $135 million. Two groups of plaintiffs opted out of the settlement and a verdict was rendered against Mylan in the amount of $12 million.

The appellees herein are four insurance companies from whom Mylan purchased insurance polices. Specifically, American Motorists Insurance Company issued two policies to Mylan which were characterized by the circuit court as general liability policies with limits of $1 million. 4 Continental Insurance Company issued two insurance policies to Mylan which were characterized by the circuit court as general liability policies with limits of $1 million. 5 Wausau Insurance *312 Company issued six policies to Mylan which were characterized by the circuit court as general liability policies of $1 million. 6 Finally, Federal Insurance Company issued an insurance policy to Mylan which the circuit court characterized as an umbrella policy with limits of liability of $10 million in excess of $1 million during the policy term of September 1, 1997 to September 1, 1998, with the policy limits on the later issued policy of $20 million in excess of $1 million. 7

The appellee insurance companies filed a declaratory judgment action in the Circuit Court of Monongalia County seeking a determination whether they have a duty to defend Mylan in the above-described litigation. Both Mylan and the appellees filed motions for summary judgment. By order dated February 8, 2007, the circuit court granted the appellees’ motions for summary judgment and denied Mylan’s motions for summary judgment. Mylan now appeals this order.

II.

STANDARD OF REVIEW

The circuit court’s order on appeal is a grant of summary judgment in a declaratory judgment. Also, the circuit court’s order is based on its construction of the language in certain insurance policies. Therefore, this Court’s standard of review in this case is de novo. See Syllabus Point 3, Cox v. Amick, 195 W.Va. 608, 466 S.E.2d 459

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Bluebook (online)
700 S.E.2d 518, 226 W. Va. 307, 2010 W. Va. LEXIS 74, Counsel Stack Legal Research, https://law.counselstack.com/opinion/mylan-laboratories-inc-v-american-motorists-insurance-wva-2010.