Could a common arthritis drug ease rare skin disease?
NCT ID NCT02113904
First seen Apr 23, 2026 · Last updated Jun 06, 2026 · Updated 9 times
Summary
This study tested the drug Humira (adalimumab) in 11 people with Netherton Syndrome, a rare genetic skin condition that causes severe inflammation, itching, and pain. The goal was to see if Humira could reduce skin symptoms by at least 20% after 3 months of treatment, with a 3-month follow-up. While not a cure, the treatment aims to control the disease and improve quality of life, though it carries risks like infection.
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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Contacts and locations
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Locations
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Necker Enfants Malades hospital
Paris, Paris, 75015, France
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
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