BASF AG v. Great American Assur

CourtCourt of Appeals for the Seventh Circuit
DecidedApril 14, 2008
Docket06-3938
StatusPublished

This text of BASF AG v. Great American Assur (BASF AG v. Great American Assur) 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 Assur, (7th Cir. 2008).

Opinion

In the United States Court of Appeals For the Seventh Circuit ____________

Nos. 06-3938, 06-3962, 06-3978, 06-4156, 06-4244 & 06-4257 BASF AG, Plaintiff-Appellee, v.

GREAT AMERICAN ASSURANCE CO., FEDERAL INSURANCE CO., and WESTCHESTER FIRE INSURANCE CO., Defendants-Appellants. ____________ Appeals from the United States District Court for the Northern District of Illinois, Eastern Division. No. 04 C 6969—Samuel Der-Yeghiayan, Judge. ____________ ARGUED NOVEMBER 30, 2007—DECIDED APRIL 14, 2008 ____________

Before BAUER, KANNE, and EVANS, Circuit Judges.Œ

Œ Following oral argument, Circuit Judge Kenneth F. Ripple disqualified himself as a member of the panel and had no role in the preparation of this decision. Circuit Judge Terence T. Evans was appointed as the third member of the panel, and was furnished with a transcript and audio recording of oral argument, as well as the briefs and the record on appeal. 2 Nos. 06-3938, 06-3962, 06-3978, 06-4156, et al.

KANNE, Circuit Judge. This insurance-coverage action represents the third case in a series of lawsuits stemming from the marketing of Synthroid, 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 dam- ages for the alleged monopolization, racketeering, fraud, and deceptive business practices of Synthroid’s producers. See Synthroid, 264 F.3d at 714. After the multi-district litigation settled, the Synthroid defendants filed the sec- ond case; that insurance-coverage suit sought damages from the Synthroid defendants’ primary-insurance provid- ers 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 de- cided that the umbrella-insurance policies required the insurers to defend BASF in the Synthroid 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. Nos. 06-3938, 06-3962, 06-3978, 06-4156, et al. 3

I. HISTORY Between 1989 and 1995, BASF’s predecessor in interest, Boots Pharmaceuticals, Inc. (“Boots”), purchased two layers of liability insurance: primary insurance and um- brella 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 out- lined 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 obli- gated 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 con- tained excess-insurance provisions, which required the

1 In March 1995, BASF acquired Boots and its related entities and completely merged the companies into a new BASF sub- sidiary, Knoll Pharmaceutical Company (“Knoll”). Incident to this transaction, Knoll and BASF assumed the benefits of the liability-insurance policies previously obtained and held by Boots. BASF sold Knoll to Abbott Laboratories (“Abbott”) in March 2001. However, pursuant to the Purchase Agreement, BASF retained its right to recover any damages from Boots’s insurers for the Synthroid litigation. For clarity, we will refer to BASF and Knoll collectively as BASF throughout this opinion. 4 Nos. 06-3938, 06-3962, 06-3978, 06-4156, et al.

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 Assur- ance Company (“Great American”), Federal Insurance Company (“Federal”), and Westchester Fire Insurance 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

2 Great American changed its name from Agricultural Insurance Company (“Agricultural”) sometime after Agricultural origi- nally issued one umbrella policy to Boots. Westchester holds three of the six umbrella policies, which were initially pro- vided to Boots by International Insurance Company and subsequently novated to Westchester. Federal issued, and continues to hold, the other two umbrella policies. Nos. 06-3938, 06-3962, 06-3978, 06-4156, et al. 5

arise out of, or because of, a personal injury or an ad- vertising 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 com- missioned 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, bioequiv- alents, 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.

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