LHC Group, Inc.v. Abbott Laboratories

Superior Court of Delaware·Decided August 11, 2023·No. N21C-11-228 PPI·Published

Opinion

IN THE SUPERIOR COURT OF THE STATE OF DELAWARE

IN RE: PROTON PUMP INHIBITORS ) Master Case No.: PRODUCTS LIABILITY LITIGATION ) C.A. No. N17C-07-001 PPI ) )

This Opinion Relates to: )

)

LHC GROUP, INC., Administrator of ) the LHC Group Benefit Plan, on ) behalf of itself and as Subrogee, )

)

Plaintiff, ) C.A. No. N21C-11-228 PPI )

v. )

)

ABBOTT LABORATORIES, et al, )

)

Defendants. )

Submitted: April 29, 20221 Decided: August 11, 2023

Upon Defendants AstraZeneca Pharmaceuticals LP, AstraZeneca LP and Merck Sharp & Dohme Corporation’s Motion to Dismiss DENIED

Upon Defendants Abbott and Takeda’s Motion to Dismiss DENIED

Thomas G. Macauley, Esquire, Macauley LLC, Wilmington, DE, Martin Bienstock, Esquire, Bienstock PLLC, Washington, D.C., Attorneys for Plaintiff LHC Group, Inc., Administrator of the LHC Group Benefit Plan, on behalf of itself and as Subrogee.

James J. Freebery, Esquire, Daniel J. Brown, Esquire, Makenzie Windfelder, Esquire, Hayley J. Reese, Esquire, Chelsea A. Botsch, Esquire, McCarter & English, LLP, Wilmington, Delaware, Arthur E. Brown, Esquire, William Hoffman, Esquire, Matthew Douglas, Esquire, Arnold & Porter Kaye Scholer LLP, New York, New York, Amy K. Fisher, Esquire, Katherine D. Althoff, Esquire, Carolyn E. Riggs, Esquire, Ice Miller LLP, Indianapolis, Indiana, Attorneys for Defendants AstraZeneca Pharmaceuticals LP, AstraZeneca LP, and Merck Sharp & Dohme Corporation.

Philip A. Rovner, Esquire, Jonathan A. Choa, Esquire, Potter Anderson & Corroon LLP, Wilmington, Delaware, Sherry Knutson, Esquire, Tucker Ellis LLP, Chicago, Illinois, Craig A.

1 D.I. No. 36. The Court last held a status conference on these matters on July 14, 2023. See In re Proton Pump Inhibitors Products Liability Litigation, C.A. No. N17C-07-001 PPI (D.I. No. 336).

Thompson, Venable LLP, Baltimore, Maryland, Attorneys for the Defendants Abbott and Takeda.

DAVIS, J.

I. INTRODUCTION

This is a personal injury action involving products liability claims. Plaintiff LHC Group,

Inc. (“LHC”)2 commenced this personal injury action against Defendants Abbott Laboratories,

AstraZeneca Pharmaceuticals LP, AstraZeneca PLC, AstraZeneca AB, Zeneca Inc., Astra US

Holding Corporation, Astra USA LLC, AstraZeneca LP,KBI Sub, Inc., GlaxoSmithKline

Consumer Healthcare Holdings (US) LLC, GlaxoSmithKline Consumer Healthcare LP,

GlaxoSmithKline Consumer Healthcare Holdings (US) IP LLC, Merck & Co. Inc. d/b/a Merck,

Sharp & Dohme Corporation, Novartis Corporation, Novartis Pharmaceutical Corporation,

Novartis Vaccines and Diagnostics, Inc., Novartis Institutes for Biomedical Research, Inc.,

Novartis Consumer Health, Inc., Pfizer, Inc., Takeda Pharmaceuticals USA, Inc., Takeda

Pharmaceuticals America, Inc., Takeda Pharmaceuticals LLC, Takeda Pharmaceuticals

International, Inc., Takeda California, Inc., Takeda Development Center Americas, Inc. f/k/a

Takeda Global Research & Development Center, Inc. Takeda Pharmaceutical Company Limited,

TAP Pharmaceutical Products, Inc. f/k/a TAP Holdings Inc., Wyeth Pharmaceuticals, Inc.,

Wyeth- Ayerst Laboratories and Wyeth LLC (collectively, “Defendants”)3 and their affiliates,

subsidiaries and/or joint venturers.

2 Amended Complaint ¶ 4 (“LHC Group brings this action as Administrator of the Plan, both directly and as subrogee of the Injured Member’s claims against Defendants pursuant to Section 11.03 of the Plan.”) (D.I. No. 36). 3 For purposes of this decision: (i) the “Abbott and Takeda Defendants” shall mean Abbott Laboratories, Takeda Pharmaceuticals USA, Inc., Takeda Pharmaceuticals America, Inc., Takeda Pharmaceuticals LLC, Takeda Pharmaceuticals International, Inc., Takeda California, Inc., Takeda Development Center Americas, Inc. f/k/a Takeda Global Research & Development Center, Inc. Takeda Pharmaceutical Company Limited, TAP Pharmaceutical Products, Inc. f/k/a TAP Holdings Inc.; and (ii) “AstraZeneca and Merck Defendants” shall mean AstraZeneca Pharmaceuticals LP, AstraZeneca PLC and Merk Sharp & Dohme Corporation (identified by LHC as Merck & Co. Inc. d/b/a Merck, Sharp & Dohme Corporation).

In the Amended Complaint, LHC asserts eleven (11) claims against Defendants. LHC

alleges that Defendants’ PPI products were dangerous to human health, defectively designed,

lacked proper warning signs, and unfit and unsuitable to be marketed and sold in the United

States. LHC seeks compensatory and punitive damages, monetary restitution, disgorgement and

an accounting, and all other available remedies.

The AstraZeneca and Merck Defendants moved to dismiss the Amended Complaint

under Civil Rule 12(b)(1). The Abbot and Takeda Defendants also moved to dismiss the

Amended Complaint, relying on Civil Rules 9(b) and 12(b)(6). The AstraZeneca and Merck

Defendants assert that the Court lacks subject matter jurisdiction over LHC’s claims. In

addition, the Abbott and Takeda Defendants contend that LHC failed to sufficiently plead its

claims and have not provided Defendants with adequate notice. In sum, Defendants collectively

moved (the “Motions”)4 to dismiss all claims asserted by LHC.

For the reasons stated below, the Court DENIES the Motions.

II. RELEVANT FACTS

A. FACTUAL BACKGROUND

LHC is a Delaware corporation with its principal place of business in Louisiana.5 LHC is

the Administrator of the LHC Group Benefit Plan (the “Plan”).6 LHC has brought its claims as

“Administrator of the Plan, both directly and as subrogee of the Injured Member’s claims against

Defendants pursuant to Section 11.03 of the Plan.”7

LHC contends that Defendants are “responsible for designing, researching, developing,

testing, manufacturing, packaging, labeling, marketing, promoting, distributing, and/or selling

4 The Motions are described more in Section II.B and Section III. 5 Am. Compl. ¶ 4. 6 Id. 7 Id.

the PPI Products including, but not limited to Dexilant, Nexium, Nexium 24HR, Prevacid,

Prevacid 24HR, Prilosec, Prilosec OTC and Protonix.”8 LHC notes that PPI products are used to

“suppress the production of acid in order to reduce the risk of duodenal ulcer recurrence and

NSAID-associated gastric ulcers as well as to treat gastroesophageal reflux disease (‘GERD’)

and certain pathological hypersecretory conditions including Zollinger-Ellison syndrome.”9

LHC brings this action as a subrogee on behalf of its Plan members who allegedly

suffered and were diagnosed with “various forms of kidney injury, which were directly and

proximately caused by their regular and prolonged use of the PPI Products.”10 Some of these

kidney injuries and diseases “include, but are not limited to, Acute Interstitial Nephritis (‘AIN’),

Acute Kidney Injury (‘AKI’), Chronic Kidney Disease (‘CKD’) and End-Stage Renal Disease

‘ESRD’).”11

B. PROCEDURAL HISTORY

On April 29, 2022, LHC filed the Amended Complaint asserting eleven counts against

Defendants.12 LHC alleges eleven cause of actions; Count I – Strict Product Liability, Count II –

Strict Product Liability – Design Defect, Count III – Strict Product Liability – Failure to Warn,

Count IV – Negligence, Count V – Negligence Per Se, Count VI – Breach of Express Warranty,

Count VII – Breach of Implied Warranty, Count VIII – Negligent Misrepresentation, Count IX –

Fraud and Fraudulent Misrepresentation, Count X – Fraudulent Concealment, Count XI –

Violation of Consumer Protection Laws and Deceptive Trade Practices.13

8 Id. ¶ 1. 9 Am. Compl. ¶ 2. 10 Id. ¶ 5. 11 Id. 12 D.I. No. 36. 13 Am. Compl. ¶¶ 245-448.

As stated above, the AstraZeneca and Merck Defendants moved to dismiss the Amended

Complaint. On May 13, 2022, the Abbott and Takeda Defendants filed the Abbott and Takeda

Defendants’ Renewed Rule 9(b) and 12(b)(6) Motion to Dismiss for Failure to State a Claim (the

“Civil Rule 12(b)(6) Motion”).14 Pfizer, Inc., Wyeth Pharmaceuticals, Inc., Wyeth- Ayerst

Laboratories and Wyeth LLC filed a joinder to the Civil Rule 12(b)(6) Motion on May 17,

2022.15 The AstraZeneca and Merck Defendants submitted their Defendants AstraZeneca

Pharmaceuticals LP, AstraZeneca LP, and Merck Sharp & Dohme Corporation’s Joinder in the

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