In Re: Testosterone Replacement Therapy Products Liability Litigation

Procedural entryThis page is a short order in In Re: Testosterone Replacement Therapy Products Liability Litigation. Read the opinion of the Court — 167 F. Supp. 3d 936
District Court, N.D. Illinois·Decided November 8, 2018·No. 1:14-cv-01748·Unknown

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE NORTHERN DISTRICT OF ILLINOIS EASTERN DIVISION

IN RE: TESTOSTERONE ) REPLACEMENT THERAPY ) Case No. 14 C 1748 PRODUCTS LIABILITY LITIGATION ) -------------------------------------------------------------- ) MDL No. 2545 THIS DOCUMENT RELATES TO: ) ALL ACTIONS )

CASE MANAGEMENT ORDER NO. 139 (Memorandum Opinion and Order on Non-Party Gemini Insurance Company's Motion to Intervene in Settlement Allocation Proceedings)

MATTHEW F. KENNELLY, District Judge: Plaintiffs in this multidistrict litigation (MDL) proceeding allege that they suffered either arterial cardiovascular injuries or injuries related to blood clots in the veins as a result of taking prescription testosterone replacement therapy (TRT) drugs. Defendants—AbbVie, Inc., Actavis, Inc., Auxilium Pharmaceuticals, Inc. (Auxilium), Eli Lilly & Company, Endo Pharmaceuticals, Inc. (Endo), GlaxoSmithKline, LLC (GSK), and affiliated entities—are manufacturers of TRT drugs. More than 7,800 individual products liability cases have been filed in the MDL, and after more than four years of litigation, a little under 6,000 remain. As of September 10, 2018, the Court has stayed all proceedings in the products liability cases, except as ordered by the Court, based on the parties' reports that they have finalized or are in the process of finalizing master settlement agreements (MSAs). Auxilium, Endo, and GSK (the Endo defendants) have reached a final MSA with plaintiffs. The MSA gives a court-appointed settlement master, Randi Ellis, the exclusive responsibility for allocating settlement funds to plaintiffs. In making allocation decisions, the settlement master carefully reviews case- specific information including records proving plaintiffs' use of TRT products. The settlement master has already spent a great deal of time on the allocation process. Non-party Gemini Insurance Company (Gemini) is one of Endo's insurers. Gemini has moved to intervene in this MDL so that it can participate in the allocation

process for claims involving the Endo defendants. For the following reasons, the Court denies Gemini's motion. Background

The Court assumes familiarity with its prior orders and discusses only the facts necessary to resolve Gemini's motion. Endo manufactures and sells two TRT products at issue in this MDL: Fortesta and Delatestryl (the Endo Products). Endo acquired Auxilium in January 2015. Auxilium manufactures and sells three TRT products at issue in this MDL: Testim, Testopel, and Striant (the Auxilium Products). Gemini insures Endo under a primary liability insurance policy. In relevant part, the policy requires Gemini, in some circumstances, to cover claims for damages allegedly caused by certain Endo pharmaceutical products and defense costs relating to such claims. Gemini has a $10 million aggregate limit of liability under the policy, which is subject to a $10 million per- event and aggregate self-insured retention. In other words, as the Court understands it, Gemini's coverage obligations do not kick in until Endo incurs $10 million in defense costs and / or payouts relating to claims that fall within the coverage provided by the policy. Gemini reimburses Endo for expenditures that exceed the $10 million retention, up to Gemini's $10 million policy limit. It is undisputed that the insurance policy does not cover claims arising from alleged use of the Auxilium Products. Gemini has moved for intervention as of right under Federal Rule of Civil Procedure 24(a)(2) and permissive intervention under Federal Rule of Civil Procedure 24(b). In its motion, Gemini contends that "[b]ecause of the $10 million [retention], Endo controlled all aspects of the [MDL] defense and, as a result, is the gatekeeper of all

information relevant to settlement, liability, and damages[.]" Gemini Mot. ¶ 7. According to Gemini, "Endo and Auxilium reached a settlement in principle with plaintiffs" on February 20, 2018 "without Gemini's knowledge or participation." Id. ¶ 9. Gemini further contends that throughout the MDL proceedings, it has understood that claims relating to the Endo Products are "largely worthless" whereas claims relating to the Auxilium Products are potentially "high-value." Id. ¶¶ 8, 11 n.2. Gemini complains that the MSA does not "distinguish between Endo product claims (insured) and Auxilium product claims (uninsured)." Id. ¶ 10. Endo, Gemini argues, must therefore be "attempting to improperly shift Auxilium's uninsured liability" to Gemini. Id. ¶ 11 n.2. Gemini seeks to intervene so that it can "participat[e] in the allocation proceedings and .

. . ensur[e] that the Special Master is fully advised of the circumstances and presented with all relevant information prior to rendering her decisions." Id. ¶ 15. Gemini also contends that Endo has refused to hand over documents Gemini believes it needs to evaluate the terms of the settlement. During a hearing on October 25, 2018, Gemini stated that if the Court grants its motion, it will formally seek discovery from Endo. Endo presents a different version of the events. The first plaintiff to assert a claim regarding an Endo Product did so in February 2014. According to Endo, it reported the lawsuit to Gemini in April 2014. Gemini responded in September 2014 by issuing a reservation of rights letter, meaning that it warned Endo it might deny coverage for some or all claims.1 Nevertheless, Gemini actively monitored the MDL, including by approving Endo's selection of defense counsel, requesting and receiving documents, and participating in regular conferences and strategy sessions with Endo and its defense counsel. In January 2018, Endo informed Gemini that settlement

negotiations "were making progress" and asked Gemini to help draft a memorandum of understanding (MOU) regarding settlement. Endo Opp. at 4-5. Gemini refused. The Endo defendants and plaintiffs reached an MOU, and on February 23, 2018, the Court stayed proceedings against the Endo defendants so that the parties could focus on finalizing an MSA. Gemini "chose not to participate in the negotiation or drafting of" the MSA, which was finalized in June 2018. Id. at 5. What Gemini did next bears emphasis: on July 17, 2018, it disclaimed any coverage of Endo for all claims in this MDL, including those arising from alleged use of the Endo Products. This fact appears nowhere in Gemini's motion, but Gemini confirmed it during the hearing on October 25, 2018. According to Endo, Gemini stated

its intention to intervene in this MDL on July 17, 2018 and again on September 11, 2018. But Gemini did not file a motion to intervene until October 12, 2018. Ten days later, Endo filed a declaratory judgment action in the Court of Common Pleas for Chester County, Pennsylvania. In the declaratory judgment action, Endo seeks, among other things, a ruling that "Gemini owes Endo the full $10 million limits of liability under the [insurance policy] for all loss and associated defense costs covered by [the policy], now that the $10 million SIR has been satisfied." Endo Mot., Ex. A (October 22, 2018

1 Endo and Gemini have not provided a copy of the letter to the Court, nor have they described the scope of the reservation of rights. Declaratory Judgment Complaint (Endo DJ Compl.)) ¶ 80. Discussion A. Intervention as of right (Fed. R. Civ. P. 24(a)(2)) "A party has a right to intervene when: (1) the motion to intervene is timely filed;

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In Re: Testosterone Replacement Therapy Products Liability Litigation, (N.D. Ill. 2018).

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