Could arthritis drug humira ease rare skin disease?
NCT ID NCT02113904
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This Phase 2 trial tested whether Humira (adalimumab), a drug used for arthritis, can help people with Netherton syndrome, a rare genetic skin condition that causes severe inflammation, itching, and pain. Eleven patients received six injections over three months, followed by three months of monitoring. The goal was to see if the drug could reduce skin symptoms by at least 20% and improve quality of life, while watching for risks like infections.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Humira (adalimumab)
- What this could lead to
- If it works, this could point toward a treatment that reduces skin inflammation and improves quality of life for people with Netherton syndrome.
- What could go wrong
- This is a small, early-phase trial with only 11 people, so results may not apply to everyone. Humira also carries risks like serious infections.
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
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
11 people
The number who actually took part.
- Started
-
Jan 2014
- Finished
-
Sep 2017
- 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
-
4 years and older
- Sex
-
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: * Patient over 4 years of age at the time of enrolment * Patient with a clinical, immuno-histochemical and/or molecular diagnosis confirmed * Vaccinations to date * Informed consent form signed by the patient and/or his parents (or the legal authority) if the patient is a child * Patient with social security coverage Exclusion Criteria: * Ongoing severe infections * Well known allergy to one of Adalimumab ingredients * Allergy to xylocaine * Ongoing treatment to immunosuppressive drugs and biotherapies * History of malignancy * Heart, renal, haematological and/or confirmed hepatic involvement * Pregnant, or breastfeeding, patients * Anomalies of the standard balance sheet: neutropenia \< 1000/mm3, polynucleose \> 12 000 / mm3 - lymphopenia \< 1000 / mm3 - anemia \< 9g / 100ml - thrombocytopenia \< 150 000 /mm3, thrombocytosis \> 500 000/mm3 - transaminase \> 3N
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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
-
Necker Enfants Malades hospital
Paris, Paris, 75015, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can an eczema drug calm a rare genetic skin disease?
- Can a skin lotion tame the symptoms of a rare genetic disease?
- Can a lotion calm the severe skin symptoms of netherton syndrome?
- New lotion shows promise for rare skin disorder
- Experimental drug for rare skin disease fails to reach goal
- Scientists hunt for clues to ichthyosis in skin and blood