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IN RE: DUPIXENT (DUPILUMAB) PRODUCTS LIABILITY LITIGATION
TRANSFER ORDER
Before the Panel:* Plaintiffs in the Southern District of California Mun, Southern District of Florida Fraioli, and Northern District of Georgia Nalls actions listed on Schedule A move under 28 U.S.C. § 1407 to centralize this litigation in the Northern District of Georgia or, in the alternative, the District of New Jersey or the Northern District of Illinois. Responding plaintiffs in six other actions listed on Schedule A support centralization in the Northern District of Georgia. Plaintiffs in five of those actions further support movants’ requested alternative transferee districts. Defendants Regeneron Pharmaceuticals, Inc. (Regeneron), Sanofi-Aventis U.S. LLC (Sanofi), and Genzyme Corporation support centralization in the Southern District of New York, or, alternatively, in the Southern District of Florida or the Middle District of Florida.
On the basis of the papers filed and the hearing session held, we find that the actions listed on Schedule A involve common questions of fact and that centralization in the District of New Jersey will serve the convenience of the parties and witnesses and promote the just and efficient conduct of the litigation. Most plaintiffs used the prescription biologic medication Dupixent, which is commonly prescribed to treat atopic dermatitis,1 and were later diagnosed with Cutaneous T-cell Lymphoma (CTCL). Other plaintiffs are the spouses or survivors of Dupixent users who were diagnosed with CTCL. Plaintiffs each allege that Dupixent caused them, their spouse, or the decedent to develop CTCL (or that Dupixent accelerated a preexisting CTCL). The parties agree that plaintiffs’ allegations will raise common questions of fact, such as (1) whether the scientific literature shows a causal link between Dupixent use and CTCL development; (2) if such a link exists, when the defendants should have learned about it; and (3) whether defendants provided adequate warnings about Dupixent's risks. With fifteen actions and seven potential tag-along actions pending across twelve districts, centralization will serve the convenience of the parties and witnesses, and conserve judicial resources.
Defendants ask us to limit the centralized proceedings to actions alleging CTCL as the injury, not other lymphomas or malignancies. Movants agree that this MDL should not include claims related to B-cell lymphoma, Hodgkin's lymphoma, or other diseases that are not T-cell lymphomas. But they oppose limiting the MDL's scope to CTCL because they allege the scientific literature links Dupixent use to non-cutaneous T-cell lymphomas, including peripheral T-cell lymphoma and anaplastic large cell lymphoma. Movants argue that the T-cell lymphoma subtypes are sufficiently similar that expert testimony and Rule 702 motions likely will overlap.
At this stage, we need not rule on whether cases involving T-cell lymphomas other than CTCL belong in this MDL. While the complaints in some of the actions cite case reports or scientific literature documenting angioimmunoblastic T-cell lymphoma and peripheral T-cell lymphoma following Dupixent use, none of the plaintiffs in the actions before us allege that they have or had a T-cell lymphoma other than CTCL or one of its subtypes. We can address the future expansion of the MDL beyond cases involving CTCL through the conditional transfer process. See Panel Rule 7.1.
The District of New Jersey is an appropriate transferee district for this litigation. Sanofi's principal place of business is in the District of New Jersey, and Regeneron, which is headquartered in nearby Tarrytown, New York, has corporate offices in the District of New Jersey. Relevant witnesses and evidence are thus likely to be in or near the District of New Jersey, which is also easily accessible for the parties and witnesses in this nationwide litigation. We assign the litigation to Judge Zahid N. Quraishi, an experienced transferee judge with the willingness and capacity to preside over this litigation. We are confident that Judge Quraishi will steer this matter on an efficient and prudent course.
IT is THEREFORE ORDERED that the actions listed on Schedule A and pending outside the District of New Jersey are transferred to the District of New Jersey and, with the consent of that court, assigned to the Honorable Zahid N. Quraishi for coordinated or consolidated pretrial proceedings.
PANEL ON MULTIDISTRICT LITIGATION
Matthew F. Kennelly Acting Chair
David C. Norton M. Casey Rodgers
Dale A. Kimball
IN RE: DUPIXENT (DUPILUMAB) PRODUCTS LIABILITY LITIGATION
MDL No. 3180
SCHEDULE A
Middle District of Alabama
WRIGHT−JENKINS v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 2:26−00087
Central District of California
BUNDY v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 5:26−00569
Eastern District of California
BELL, ET AL. v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 2:26−00320
Southern District of California
MUN v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 3:26−00127
Middle District of Florida
DURKIN v. SANOFI−AVENTIS U.S. LLC, ET AL., C.A. No. 2:26−00231
Southern District of Florida
FRAIOLI v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 1:26−20636
Northern District of Georgia
NALLS v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 1:25−07342
STREET, ET AL. v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 1:26−00493
LONG, ET AL. v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 1:26−00635
SEALS v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 1:26−00813
Northern District of Illinois
WALSH v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 1:25−15265
District of New Jersey
PHILLIPS v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 2:25−18162
District of Nevada
LUCHSINGER, ET AL. v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 2:26−00338
Eastern District of Pennsylvania
BOGGS, ET AL. v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 2:26−00763
Middle District of Tennessee
RICHARDSON v. REGENERON PHARMACEUTICALS, INC., ET AL., C.A. No. 3:25−01125
FOOTNOTES
FOOTNOTE. Judge Karen K. Caldwell and Judge Madeline Cox Arleo took no part in the decision of this matter.
1. Atopic dermatitis is commonly known as eczema.
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Docket No: MDL No. 3180
Decided: June 04, 2026
Court: United States Judicial Panel on Multidistrict Litigation.
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