Cheap arthritis drug could tame severe eczema
NCT ID NCT00809172
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether methotrexate, an older drug used for arthritis, works as well as cyclosporine for people with moderate to severe atopic dermatitis (eczema). One hundred adults received either drug for 24 weeks. The main goal was to see if eczema severity dropped by half after 8 weeks. Researchers also tracked quality of life and side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- methotrexate and cyclosporine
- What this could lead to
- If methotrexate works as well as cyclosporine, it could offer a safer long-term option for controlling severe eczema.
- What could go wrong
- This is a small, completed trial comparing two existing drugs. Neither is a cure, and both have side effects like kidney or liver risks.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
100 people
The number who actually took part.
- Start date
-
Dec 2008
- Finished
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Apr 2012
- Lead sponsor
-
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
-
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: * Patients aged \> 18 years old. * Both genders eligible for study. * Moderate to severe AD. * Scorad \> 15. * Participants must use a contraceptive method during the trial and for 3 months after the end of the trial for female and 5 months for male participants. * Participants must be able to understand and sign the Informed Consent, and comply with all aspects of the protocol. * Patients must be registered in a social security system or with a health insurance coverage. Exclusion Criteria: * Pregnant or lactating women. * Evolutive skin disease. * Patients with a clinically significant disease (chronic, recurrent or active). * Systemic corticotherapy or immunosuppressive treatment during the previous month, or local corticoid the week before the inclusion. * Contra-indication to methotrexate and cyclosporine. * Exposure to phototherapy: cumulative dose \> 2000 J/cm2. * Patients deprived of their civic rights, in custody, or subject to a tutorial, judiciary or administrative decision. * Patients under a protection measure. * Patients in a critical medical situation. * Patients with a personal situation evaluated by the investigator as unable to give optimal participation to the study, or where the study could constitute a risk for the patient.
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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
-
Hospices Civils de Lyon
Lyon, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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