Mycosis Fungoides and Dupixent Lawsuits
Diagnosed With Mycosis Fungoides After Taking Dupixent?
Mycosis fungoides is the most common form of cutaneous T-cell lymphoma. It can look like eczema for years before it is correctly diagnosed. Lawsuits allege that the makers of Dupixent failed to warn patients and doctors about a possible link between the drug and this cancer. If you used Dupixent and were later diagnosed with mycosis fungoides, you may be eligible to file a claim.
- No fee unless you recover
- 100% confidential
- Nationwide claims
- Consolidated in federal court
What Is Mycosis Fungoides?
Mycosis fungoides is the most common type of cutaneous T-cell lymphoma, a cancer that begins in the T-cells of the immune system and shows up in the skin. It is usually slow-growing and develops over time, often moving through stages. In its early stages it appears as flat, scaly patches. As it progresses it can form raised plaques and, in later stages, tumors on the skin. In advanced disease it can spread to the lymph nodes, blood, or internal organs.
What makes mycosis fungoides especially relevant to the Dupixent litigation is how easily it is mistaken for something else. In its early stages it can look almost identical to eczema, psoriasis, or ordinary dermatitis. Many patients are treated for a benign skin condition for months or years before a biopsy reveals the truth.
Why Mycosis Fungoides Is Central to These Cases
Dupixent is frequently prescribed for eczema. Early mycosis fungoides often looks like eczema. That overlap sits at the center of the lawsuits. Plaintiffs allege two related harms. First, that Dupixent may trigger or accelerate T-cell lymphoma in some patients. Second, that by calming the visible skin symptoms, the drug may have masked an underlying mycosis fungoides, delaying the biopsy and diagnosis that could have caught the cancer earlier.
Peer-reviewed studies have reported elevated rates of cutaneous T-cell lymphoma, including mycosis fungoides, among patients treated with Dupixent. As of June 2026, the FDA-approved label for Dupixent still does not carry a specific warning about CTCL or lymphoma, even though the FDA has identified CTCL as a potential safety signal tied to the drug. The lawsuits allege the manufacturers had access to this information and did not adequately warn.
Signs and Symptoms Patients Report
- Flat, scaly patches that resemble eczema or psoriasis and do not clear with treatment
- Raised, thickened plaques on the skin
- Severe, persistent itching
- Patches that appear in areas not usually exposed to the sun
- Skin tumors in later stages
- Swollen lymph nodes as the disease advances
Where the Cases Stand
On June 4, 2026, federal Dupixent T-cell lymphoma cases were consolidated into MDL No. 3180 in the U.S. District Court for the District of New Jersey before Judge Zahid N. Quraishi. The defendants are Regeneron Pharmaceuticals and Sanofi-Aventis U.S. The litigation is in its early stages, which makes this a timely moment to have your potential claim reviewed. No settlements have been reached, and no outcome is guaranteed.
Current as of June 2026. The litigation is active and ongoing. No settlements have been reached, and no outcome is guaranteed.
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