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Marin & Murphy is licensed in South Carolina, Massachusetts, Rhode Island, and Connecticut, and works with lawyers licensed across the country.
Marin & Murphy is not licensed in Pennsylvania; a matter there would be handled with, or referred to, a lawyer licensed in that state.
Dupixent — CTCL Litigation
The Dupixent Litigation, Explained
Federal cases are consolidated in MDL 3180, most cases are in their earliest stages, and no settlement exists. Here is what is publicly known.
ACTIVE LITIGATION — NO SETTLEMENT. MDL 3180 underway · deadlines vary by state.
Marin & Murphy is not licensed in Pennsylvania; details below.
Partners
Stefanie A. Murphy & Matthew T. Marin
Super Lawyers® honorees · members of the American Association for Justice · concentrating in personal injury and mass-tort litigation.
No settlement has been reached in the Dupixent litigation, and most cases are in their earliest stages. Every case must be proven on its own facts. Whether any patient has a claim depends on the facts and the law of their state. The information below covers the litigation itself.
Marin & Murphy Law Firm is not licensed in Pennsylvania; details below.
The allegation, in Pennsylvania and nationwide, is an association between Dupixent (dupilumab) and cutaneous T-cell lymphoma; no court has found Dupixent causes CTCL, and no settlement of any kind exists. Whether any individual has a claim depends on their medical records and the law of their state. The information below covers the litigation itself.
Where Things Stand in the Dupixent CTCL Litigation
In Pennsylvania as nationwide, Dupixent (dupilumab) — a prescription biologic made by Sanofi and Regeneron, FDA-approved since March 2017 — now carries nine indications, including atopic dermatitis, asthma, and COPD. For Pennsylvania claimants, the operative order came in June 2026, when the Judicial Panel on Multidistrict Litigation centralized the pending federal cases as MDL 3180 in the United States District Court for the District of New Jersey, before Judge Zahid N. Quraishi. The complaints in the consolidated Dupixent lawsuit allege that the drug is associated with an increased risk of cutaneous T-cell lymphoma (CTCL) and that the manufacturers failed to warn patients and doctors. The MDL that would receive a case from Pennsylvania counted 38 pending cases as of October 1, 2026; the MDL 3180 tracker keeps the current count and its method. No court has ruled on the merits of any Dupixent claim — from Pennsylvania or anywhere else — and no settlement exists.
What the Filings Allege — and What They Do Not
An association is alleged; no court, in Pennsylvania or elsewhere, has adjudicated it as fact. Published studies report a statistical association between dupilumab and CTCL — an association the study authors themselves note does not establish causation — and the FDA has identified a potential safety signal for CTCL that it is still evaluating. Dupixent’s label — the same label patients in Pennsylvania see — currently contains no lymphoma or malignancy warning. The FDA adverse event reports connected to this question are agency reports, not verified causes, and the courts have decided nothing on the merits — in Pennsylvania or anywhere else.
Pennsylvania Residents in the Dupixent MDL: Two Docketed Cases
A Pennsylvania resident filed one of the earliest Dupixent CTCL lawsuits, Boggs v. Regeneron Pharmaceuticals, Inc., in the Eastern District of Pennsylvania on February 6, 2026 (No. 2:26-cv-00763, public docket). The 119-page complaint alleges that the plaintiff used Dupixent for atopic dermatitis from approximately 2020 until February 2023 and was thereafter diagnosed with cutaneous T-cell lymphoma; it names Regeneron Pharmaceuticals, Inc., Sanofi-Aventis U.S. LLC, and Genzyme Corporation, pleads a failure to warn, and includes a spouse’s loss-of-consortium claim. Pennsylvania has a second docketed filing on this track, Hinton (Eastern District of Pennsylvania, March 2026, pleading a mycosis fungoides diagnosis after injections in 2025). Both were transferred to MDL 3180 in the District of New Jersey. These are allegations from a complaint; no court has ruled on them, and no settlement exists.
Who the Filed Cases Include
For Pennsylvania families reviewing the criteria: the consolidated cases involve Dupixent use followed by a diagnosis of cutaneous T-cell lymphoma or a related T-cell lymphoma subtype during or after that use. There is no minimum length of Dupixent use required; in Pennsylvania, estates of patients who have died bring claims under state wrongful-death and survival statutes. Whether any individual’s circumstances resemble the filed cases is a question of medical records and state law, not of headlines — and for a Pennsylvania resident, it is a question for an attorney licensed in Pennsylvania.
Pennsylvania’s Federal Courts and the Path to MDL 3180
Pennsylvania is served by three federal district courts: the United States District Court for the Eastern District of Pennsylvania; the United States District Court for the Middle District of Pennsylvania; and the United States District Court for the Western District of Pennsylvania. No Dupixent CTCL lawsuit filed there proceeds alone — the Judicial Panel on Multidistrict Litigation has centralized these cases as MDL 3180 before Judge Zahid N. Quraishi in the United States District Court for the District of New Jersey, so a Pennsylvania case is transferred to the MDL for coordinated pretrial proceedings — or, where the MDL court’s case-management orders permit, filed in the District of New Jersey directly. Both routes end in the same consolidated proceeding; every case, including any from Pennsylvania, remains an individual claim — an MDL is not a class action.
Filing Deadlines Under Pennsylvania Law
Pennsylvania’s general statute of limitations for personal-injury claims is two years under 42 Pa. Cons. Stat. § 5524. Pennsylvania applies a discovery rule: accrual is deferred until the plaintiff knows, or reasonably should know, that she has been injured and that the injury was caused by another party’s conduct. How a limitations period applies to any specific CTCL diagnosis depends on the dates in the medical records, the legal theory pleaded, and Pennsylvania tolling and accrual doctrine. An attorney licensed in Pennsylvania can evaluate whether a claim is timely.
A wrongful-death claim carries a two-year period that begins at death (42 Pa. C.S. § 5524(2)), brought by the personal representative.
How Common Is CTCL in Pennsylvania?
Pennsylvania is home to about 13.1 million people (U.S. Census Bureau, 2024 estimate). Cutaneous T-cell lymphoma is rare — roughly 8.55 new cases per million person-years (SEER) — which works out to on the order of 110 new CTCL diagnoses across Pennsylvania in a typical year. That rarity is why no statistic on this page can answer an individual question from Pennsylvania: medical records, read against state law, decide any single claim.
About Marin & Murphy Law Firm and Pennsylvania
Marin & Murphy Law Firm is a personal-injury and mass-tort law firm; its attorneys’ individual admissions are listed at the bottom of this page, and this page is published as litigation information. Marin & Murphy Law Firm is not licensed in Pennsylvania. The firm does not accept Pennsylvania legal matters; inquiries from Pennsylvania residents are referred to attorneys licensed in Pennsylvania. Some matters may be referred to other lawyers. An attorney licensed in Pennsylvania can evaluate whether a claim is timely and how Pennsylvania law applies to a particular diagnosis.
Pennsylvania Dupixent Litigation FAQs
Are there Dupixent lawsuits in Pennsylvania courts?
The federal cases are consolidated in MDL 3180 in the District of New Jersey; a case from Pennsylvania would join that proceeding rather than proceed separately. A Dupixent CTCL case filed in a Pennsylvania federal court is subject to transfer into that consolidated proceeding. This page does not track filings outside the federal system.
Who is included in the filed cases?
Anyone — residents of Pennsylvania included — who used Dupixent and was diagnosed with cutaneous T-cell lymphoma or a related T-cell lymphoma subtype during or after that use. The claims do not depend on a minimum duration of use, and in Pennsylvania, estates of patients who have died bring claims under state wrongful-death and survival statutes.
Has any court found that Dupixent causes CTCL?
No. What exists, in Pennsylvania as everywhere: an alleged association; published studies reporting a statistical association their authors note does not establish causation; an FDA evaluation of a potential safety signal that is still under way; and a Dupixent label with no lymphoma warning.
Is there a Dupixent settlement?
No. No settlement exists, no court has ruled on the merits, and — for Pennsylvania claimants as for all others — the litigation is in its earliest stages. If a figure suggests otherwise to someone in Pennsylvania, it did not come from the docket.
What is the filing deadline for a Pennsylvania Dupixent claim?
Filing deadlines come from Pennsylvania statutes and court doctrine, and more than one rule can bear on when the period begins to run; the section above covers what is settled and what is not. An attorney licensed in Pennsylvania can evaluate whether a claim is timely.
Does Marin & Murphy Law Firm accept Pennsylvania cases?
No. Marin & Murphy Law Firm is not licensed in Pennsylvania and does not accept Pennsylvania legal matters; inquiries from Pennsylvania residents are referred to attorneys licensed in Pennsylvania.
Nearby states
Dupixent in Pennsylvania: Prescription Data at a Glance
Dupixent (dupilumab), prescribed most often for atopic dermatitis and other inflammatory conditions, is in wide use across Pennsylvania. Federal utilization reporting puts numbers on that use:
Pennsylvania saw its reported Medicaid prescription count grow by about 17% between 2024 and 2025. In 2025, Medicaid reimbursement for Dupixent in Pennsylvania totaled $137.1 million. These figures cover Medicaid outpatient utilization only — they do not include prescriptions paid through Medicare or private insurance, so the total number of residents of Pennsylvania using Dupixent is higher. Totals exclude a small number of records the program suppresses for privacy.
1 of the 15 actions on Schedule A of the transfer order was filed in Pennsylvania federal court before the Judicial Panel on Multidistrict Litigation centralized the Dupixent lawsuits into MDL 3180 in the District of New Jersey on June 4, 2026.
Sources: Centers for Medicare & Medicaid Services, State Drug Utilization Data 2024 and 2025 (accessed August 21, 2026); In re: Dupixent (Dupilumab) Products Liability Litigation, MDL No. 3180, JPML Transfer Order, Schedule A (June 4, 2026). Utilization data reflects prescriptions reported by state Medicaid programs and is not evidence that any individual prescription caused injury.
Sources
- U.S. Judicial Panel on Multidistrict Litigation, Pending MDL Dockets by MDL Number (October 1, 2026) — jpml.uscourts.gov
- MDL 3180 docket records — CourtListener dockets 72288297 (JPML) and 73443394 (D.N.J. 3:26-md-03180), reviewed September 15, 2026.
- 42 Pa. Cons. Stat. § 5524 — Pennsylvania statute of limitations discussed above.
- U.S. Census Bureau, Vintage 2024 Population Estimates (NST-EST2024), resident population as of July 1, 2024.
- SEER program data: cutaneous T-cell lymphoma incidence ≈8.55 cases per million person-years.
Marin & Murphy Law Firm is not licensed in Pennsylvania. The firm does not accept Pennsylvania legal matters; inquiries from Pennsylvania residents are referred to attorneys licensed in Pennsylvania. Some matters may be referred to other lawyers.
Attorney admissions: Matthew T. Marin — RI, CT, MA, SC, U.S.D.C. D.R.I. · Stefanie A. Murphy — RI, CT, MA, U.S.D.C. D.R.I./D.Conn./D.Mass.
Attorney Advertising.
Attorney Advertising. This page is for general information and is not legal advice; reading it does not create an attorney-client relationship, and no attorney-client relationship is formed until a written engagement agreement is signed. Marin & Murphy Law Firm attorneys are licensed in Rhode Island, Connecticut, Massachusetts, and South Carolina; the firm’s mass-tort practice is directed from its Charleston, South Carolina office. Responsible attorney: Matthew T. Marin, 997 Morrison Drive, Suite 200, Charleston, SC 29403. Cases may be handled together with co-counsel; whether a claim is accepted is determined after review. No representation is made that the quality of legal services is greater than that of other lawyers. Prior results do not guarantee a similar outcome; every case depends on its own facts.
Where we practice
Marin & Murphy Law Firm attorneys are licensed in Rhode Island, Connecticut, Massachusetts, and South Carolina. We are not licensed in Pennsylvania. The firm does not accept Pennsylvania legal matters; inquiries from Pennsylvania residents are referred to attorneys licensed in Pennsylvania. This page is attorney advertising and is provided for general information; it is not legal advice, and reading it does not create an attorney–client relationship.