Eczema drug switch studied after first treatment fails
NCT ID NCT06773455
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether a drug called tralokinumab could help adults with eczema who had already tried dupilumab and didn't get enough relief. The plan was to treat 20 people for 24 weeks, but the study was stopped early and only 7 people took part. The main goal was to see how many achieved clear or almost clear skin by week 16.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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7 people
The number who actually took part.
- Started
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Sep 2023
- Finished
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Jan 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Male or female adult ≥ 18 years of age; * All participants must have prior treatment with dupilumab for atopic dermatitis meeting one of the following conditions: * Participants who stopped dupilumab treatment due to non-response, partial response, loss of efficacy must have been previously treated with dupilumab for at least 12 weeks. * Participants who stopped dupilumab treatment due to intolerance or AEs to the drug may enter the study with no required prior length of dupilumab treatment. AE's must be resolved prior to 1st tralokinumab dose. * Females of childbearing potential (FCBP) must have a negative urine pregnancy test at Baseline. FCBP who engage in activity in which conception is possible must use one of the approved contraceptive options: hormonal contraception; intrauterine device (IUD); tubal ligation; or partner's vasectomy; Male or female condom diaphragm with spermicide, cervical cap with spermicide, or contraceptive sponge with spermicide. Subject is a candidate for systemic therapy. * Subject must be in general good health as judged by the Investigator, based on medical history, physical examination. * Able and willing to give written informed consent prior to performance of any study-related procedures. Exclusion Criteria: * Subjects with previous exposure to tralokinumab. * Known or suspected hypersensitivity to tralokinumab or any of its excipients. * Women of childbearing potential who are pregnant, intend to become pregnant, or are lactating. * Use of tanning beds or phototherapy within 4 weeks of baseline * Use of systemic therapies (systemic steroids, cyclosporine, oral JAK inhibitors etc.) for atopic dermatitis within 4 weeks * Patient non-compliant with Dupixent dosing based on investigator discretion. * Any clinically significant (as determined by the investigator) cardiac, endocrinologic, pulmonary, neurologic, psychiatric, hepatic, renal, hematologic, immunologic disease, or other major disease that is uncontrolled.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Psoriasis Treatment Center of New Jersey
East Windsor, New Jersey, 08520, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a daily liquid medicine calm severe eczema in toddlers and preschoolers?
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- Can a Lab-Made antibody calm severe eczema?
- Is your nose fueling infected eczema and scabies sores?
- Can an eczema drug reshape the Skin's microbial community?