In re Invokana (CANAGLIFLOZIN) Products Liability Litigation

223 F. Supp. 3d 1345, 2016 U.S. Dist. LEXIS 189121, 2016 WL 7221425
CourtUnited States Judicial Panel on Multidistrict Litigation
DecidedDecember 7, 2016
DocketMDL No. 2750
StatusPublished
Cited by6 cases

This text of 223 F. Supp. 3d 1345 (In re Invokana (CANAGLIFLOZIN) Products Liability Litigation) is published on Counsel Stack Legal Research, covering United States Judicial Panel on Multidistrict Litigation primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
In re Invokana (CANAGLIFLOZIN) Products Liability Litigation, 223 F. Supp. 3d 1345, 2016 U.S. Dist. LEXIS 189121, 2016 WL 7221425 (jpml 2016).

Opinion

TRANSFER ORDER

Sarah S. Vance, Chair

Before the Panel: * Plaintiffs in 29 actions pending in the District of New Jersey move under 28 U.S.C. § 1407 to centralize this litigation in that district. The [1347]*1347litigation consists of 55 actions, as listed on the attached Schedule A. The Panel has been informed of 44 additional related federal actions.1

The 55 actions involve allegations that ingestion of the drug Invokana may cause a variety of injuries, including diabetic ke-toacidosis and kidney damage, and that defendant Janssen Pharmaceuticals, Inc. (Janssen), which developed and manufactured the drug, failed to adequately test the drug and warn of its risks. Invokana and its sister drug Invokamet2 belong to a class of diabetes drugs known as Sodium Glucose Cotransporter 2 (SGLT2) inhibitors. Other SLGT2 inhibitors include Farxiga (dapagliflozin) and Jardiance (em-pagliflozin). Farxiga is marketed and distributed by AstraZeneca Pharmaceuticals LP, AstraZeneca LP, AstraZeneca AB, AstraZeneca PLC, and Bristol-Myers Squibb Co. (collectively the Farxiga Defendants), and Jardiance is marketed and distributed by Boehringer Ingelheim Pharmaceuticals, Inc., Eli Lilly and Company, and Lilly USA, LLC (collectively the Jar-diance Defendants). Of the 55 actions, only one, the Western District of Kentucky House action, is a so-called “combination case”—an action involving ingestion of not only Invokana or Invokamet but also another SGLT2 inhibitor (in this case, Farxi-ga).

The central dispute concerning centralization is whether the proposed MDL should include only Invokana/Invokamet cases or cases involving other SGLT2 inhibitors, including Farxiga and Jardiance.3 Moving plaintiffs, as well as plaintiffs in certain other actions, support centralization of only Invokana/Invokamet cases, but differ, to some extent, regarding the choice of a transferee district. Plaintiffs in six District of New Jersey constituent actions (Erway, Johnston, Mullin, Puente, Sanders, and Sarkisyan) and three District of New Jersey potential tag-along action (Aris, Monot, and Plott) support centralization of the Invokana/Invokamet cases in the District of New Jersey.4 Plaintiffs in four Southern District of Illinois constituent actions (Allen, Counts, Freeman, and Schurman) and the Western District of Kentucky House constituent action support centralization of the Invokana/Invoka-met cases in the Southern District of Illinois (or, in the alternative, the District of New Jersey). Plaintiff in an Eastern District of Missouri potential tag-along action (Seamon) supports centralization of Invo-kana/Invokamet cases in the Eastern District of Missouri (or, in the alternative, the District of New Jersey).

Plaintiff in the constituent District of Minnesota Schroeder action, as well as plaintiffs in two potential tag-along actions5 (collectively the Schroeder Plaintiffs), argue for “class-wide” centralization, in the Northern District of Illinois, of cases involving not only Invokana but also Farxiga and Jardiance. Plaintiffs in seven potential tag-along actions6 support the [1348]*1348Schroeder Plaintiffs’ position in its entirety. Plaintiffs in eight potential tag-along actions7 support class-wide centralization, but in the District of New Jersey. Plaintiff in a potential tag-along action (.Martin) in the Northern District of West Virginia supports class-wide centralization, but in the Northern District of West Virginia (or, in the alternative, the Northern District of Illinois).

Janssen supports centralization of only Invokana/Invokamet in the District of New Jersey (or, in the alternative, the Northern District of Illinois). The Farxiga Defendants oppose inclusion of any Farxiga claims or cases in the proposed MDL. If the Panel orders class-wide centralization over their objections, then the Farxiga Defendants favor centralization in either the District of New Jersey or the Northern District of Illinois. The Jardiance Defendants oppose inclusion of any Jardiance claims or cases in the proposed MDL.

On the basis of the papers filed and the hearing session held, we find that the Invokana/Invokamet actions involve common questions of fact, and that centralization of these cases will serve the convenience of the parties and witnesses and promote the just and efficient conduct of this litigation. The actions share factual questions arising from allegations that taking Invokana or Invokamet may result in patients suffering various injui-ies, including diabetic ketoacidosis and kidney damage. The actions thus implicate numerous common issues concerning the development, manufacture, testing, regulatory history, promotion, and labeling of the drugs. Centralization will eliminate duplicative discovery, prevent inconsistent pretrial rulings on Dauberb issues and other pretrial matters, and conserve the resources of the parties, them counsel, and the judiciary.

On the current record, we are not convinced that the MDL should include claims involving Farxiga, Jardiance, or any other SLGT2 inhibitor, including any such claims in “combination cases.” We are “typically hesitant to centralize litigation against multiple, competing defendants which marketed, manufactured and sold similar products.” See, e.g., In re: Yellow Brass Plumbing Component Prods. Liab. Litig., 844 F.Supp.2d 1377, 1378 (J.P.M.L. 2012). Centralizing competing defendants in the same MDL may unnecessarily complicate case management, due to the need to protect trade secret and confidential information. See, e.g., In re: Watson Fentanyl Patch Prods. Liab. Litig., 883 F.Supp.2d 1350, 1351 (J.P.M.L. 2012) (“Centralization of all actions against all manufacturers will add few efficiencies to the resolution of this litigation,” and “could complicate these matters, as defendants may need to erect complicated confidentiality barriers, since they are business competitors.”). In addition, a multi-defen-dant MDL may prolong pretrial proceedings, because of, inter alia, the possible need for separate discovery and motion tracks, as well as the need for additional bellwether trials. Here, especially given the relatively small number of Farxiga-only cases (fifteen), Jardianee-only cases (three), and “combination cases” (three), we conclude that class-wide centralization is not warranted at the present time.

We select the District of New Jersey as transferee district for this litigation. Janssen is headquartered in that district, and many witnesses and relevant documents are likely to be found there. In [1349]*1349addition, 37 of the constituent actions are pending in that district, as are multiple tag-along actions. Finally, centralization in the District of New Jersey allows us to assign the litigation to Judge Brian R. Martinotti, an able and experienced jurist who has not had the opportunity to preside over an MDL. Judge Martinotti already is presiding over the constituent and tag-along actions pending in the district, and we are confident that he will steer this litigation on a prudent course.

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Cite This Page — Counsel Stack

Bluebook (online)
223 F. Supp. 3d 1345, 2016 U.S. Dist. LEXIS 189121, 2016 WL 7221425, Counsel Stack Legal Research, https://law.counselstack.com/opinion/in-re-invokana-canagliflozin-products-liability-litigation-jpml-2016.