BASF AG v. Great American Assurance Co.

522 F.3d 813, 2008 U.S. App. LEXIS 8085
CourtCourt of Appeals for the Seventh Circuit
DecidedApril 14, 2008
Docket06-3938, 06-3962, 06-3978, 06-4156, 06-4244 and 06-4257
StatusPublished
Cited by62 cases

This text of 522 F.3d 813 (BASF AG v. Great American Assurance Co.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Seventh Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
BASF AG v. Great American Assurance Co., 522 F.3d 813, 2008 U.S. App. LEXIS 8085 (7th Cir. 2008).

Opinion

KANNE, Circuit Judge.

This insurance-coverage action represents the third case in a series of lawsuits stemming from the marketing of Syn-throid, a synthetic thyroid drug. See In re Synthroid Mktg. Litig., 264 F.3d 712 (7th Cir.2001); Knoll Pharm. Co. v. Auto. Ins. Co., 152 F.Supp.2d 1026 (N.D.Ill.2001). The first case — a multi-district litigation— consolidated numerous class actions filed by consumers and health insurers that sought damages for the alleged monopolization, racketeering, fraud, and deceptive business practices of Synthroid’s produc *815 ers. See Synthroid, 264 F.3d at 714. After the multi-district litigation settled, the Synthroid defendants filed the second case; that insurance-coverage suit sought damages from the Synthroid defendants’ primary-insurance providers for the insurers’ alleged failure to defend them in, and indemnify them for, the settlement of the multi-district litigation. See Knoll Pharm. Co., 152 F.Supp.2d at 1031. While it was pending on appeal, the second case also settled.

German corporation BASF AG (“BASF”) then filed this third suit, seeking to recover damages from its umbrella insurers for their failure to defend and indemnify BASF, and its related corporate entities, in the initial Synthroid litigation. The district court in this case decided that the umbrella-insurance policies required the insurers to defend BASF in the Syn-throid litigation, and granted summary judgment to BASF on the insurers’ liability for breach of contract. We disagree. The terms of the umbrella policies, as a matter of law, did not obligate the insurers to defend or indemnify BASF. We therefore reverse, and remand to the district court for the entry of summary judgment in favor of the insurers.

I. History

Between 1989 and 1995, BASF’s predecessor in interest, Boots Pharmaceuticals, Inc. (“Boots”), purchased two layers of liability insurance: primary insurance and umbrella insurance. 1 The primary-insurance policies all contained similar provisions, which stated that the insurers would indemnify Boots for lawsuits seeking damages “arising out of’ claims for a “personal injury” or an “advertising injury.” The primary policies uniformly defined an “advertising injury” as, among other things, an “injury arising out of ... oral or written publication of material that slanders or libels a person or organization or disparages a person’s or organization’s goods, products, or services.” Moreover, the primary policies each outlined the insurer’s duty to defend: each primary policy required the insurer to pay all costs that Boots incurred in defense of any suit for which the insurer would be obligated to indemnify Boots.

The umbrella-insurance policies provided two additional types of insurance coverage to Boots: excess coverage and gap-filling coverage. All of the umbrella policies contained excess-insurance provisions, which required the umbrella insurers to indemnify Boots for sums Boots became liable for that exceeded the coverage limits of its primary-insurance policies. Some of the umbrella policies also included gap-filling-insurance provisions, which obligated the umbrella insurers to defend Boots for any loss covered by the terms and conditions of the umbrella policy, and “not covered as warranted” by the primary insurers. Other umbrella policies described this gap-filling coverage as the obligation to defend any suit or any claim potentially covered by the umbrella policies to which the primary policies did not apply.

The defendants in this action — Great American Assurance Company (“Great American”), Federal Insurance Company (“Federal”), and Westchester Fire Insur- *816 anee Company (“Westchester”) — hold six of these umbrella-insurance policies. 2 Like the primary-insurance policies, the umbrella policies covered only lawsuits that sought damages “arising out of’ or “because of’ a “personal injury” or an “advertising injury.” The umbrella policies all defined personal injury and advertising injury in a manner that was substantively identical to the primary policies’ definitions of those terms. Put another way, exclusions aside, the primary policies’ and umbrella policies’ coverage of personal injury and advertising injury was coextensive, and a suit or claim that did not arise out of, or because of, a personal injury or an advertising injury would not be covered under either the primary or the umbrella policies.

In 1987, Boots began to manufacture, market, and sell Synthroid, a synthetic thyroid medication used to treat various thyroid diseases. In an attempt to prove that Synthroid was superior to competing synthetic thyroid hormones on the market, in the late 1980s Boots commissioned a study by Dr. Betty Dong of the University of California-San Francisco (“UCSF”). Boots hoped the study would prove that Synthroid and its competitors (among them, cheaper generic hormones) were not “bioequivalents” — drugs that have the same effect on a patient in terms of potency and absorption rate when equal doses are administered. See Synthroid, 264 F.3d at 714. However, in 1990, Dr. Dong discovered that Synthroid and its competitors were, in fact, bioequivalents, and that all of the compared synthetic hormones, including the cheaper generics, were as effective as Synthroid at treating thyroid diseases.

When provided with these results, Boots immediately sought to discredit Dr. Dong and her findings. Boots’s scientists sent letters to Dr. Dong that questioned her methods and conclusions, and Boots asked UCSF to terminate the study. UCSF did not comply and in 1994, Dr. Dong provided her final report to Boots, which stated that Synthroid and its competitors were bioe-quivalents. Even after Boots learned of Dr. Dong’s results, Boots continued to publicly maintain that Synthroid had no known bioequivalents, and Boots continued to advertise and market the drug as such. In early 1995, Boots exercised its rights under its contract with Dr. Dong to block the publication of her study.

In 1996, the Wall Street Journal learned of Dr. Dong’s study and Boots’s response, and it published an exposé on Boots and Synthroid. The article revealed to the public that there were cheaper alternatives to Synthroid, and that Boots had prevented the publication of Dr. Dong’s study, which had confirmed that the cheaper alternatives were equally effective. Dr. Dong’s study was eventually published in 1997. See Synthroid, 264 F.3d at 714. On the heels of the Wall Street Journal article and the publication of Dr. Dong’s study, over 70 lawsuits (mostly class actions) were filed against BASF and its employees. These suits, filed by consumers and health insurers, alleged a potpourri of antitrust, racketeering, fraud, misrepresentation, deceptive-business-practices, and unjust-enrichment claims all based on the fact that Boots had deceived consumers into purchasing Synthroid, which occupied 70% of the $600 million market for thyroid drugs at the time. In 1997, the lawsuits were consolidated into a multi-district liti

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Bluebook (online)
522 F.3d 813, 2008 U.S. App. LEXIS 8085, Counsel Stack Legal Research, https://law.counselstack.com/opinion/basf-ag-v-great-american-assurance-co-ca7-2008.