Promising drug for hand and foot blisters falls short in early trial
NCT ID NCT05710185
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a daily pill called deucravacitinib in 3 adults with palmoplantar pustulosis (PPP), a painful skin condition causing blisters on palms and soles. The goal was to see if the drug could reduce disease severity by at least 50% over 24 weeks. However, the trial was terminated early, so results are limited.
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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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3 people
The number who actually took part.
- Started
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Jul 2023
- Finished
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Jan 2025
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * • Adults aged 18 years of age and older * Dermatologist confirmed diagnosis of PPP for at least 6 months * Moderate-severe PPP, defined as a ppPASI \> 12 * Inadequate response to topical therapy and a candidate for systemic or phototherapy * Willing to discontinue current topical and/or systemic PPP treatments, except for OTC emollients Exclusion Criteria: * • Participants with other immune-mediated conditions requiring concurrent systemic immunosuppressant treatments * Current/recent administration of PPP-specific medications including: * Rituximab within 6 months of the baseline visit * Biologics within 12 weeks of baseline visit * Systemic steroids, oral immunosuppressants (azathioprine, cyclosporine, methotrexate, mycophenolate mofetil, tacrolimus), oral retinoids (acitretin, isotretinoin), apremilast, or dapsone within 4 weeks of baseline visit * Phototherapy within 4 weeks of baseline visit * Prescription topical medications (including calcineurin inhibitors, crisaborole, retinoids, steroids, tar, vitamin D analogs) within 2 weeks of baseline visit * History of active infection and/or febrile illness within 7 days; or infection requiring antibiotic treatment within 30 days; or serious infection requiring hospitalization and/or IV antibiotics within 90 days * Evidence of other infection including: * Active or untreated latent tuberculosis, defined as radiographic or laboratory evidence of active TB or positive quantiferon or PPD, unless the subject has completed the recommended treatment * Human immunodeficiency virus infection (positive HIV antibody) * Active hepatitis B * Active hepatitis C * Evidence of clinically significant laboratory abnormality including: * Absolute WBC count \< 3000/mm3 * Platelet count \< 100,000/mm3 * Hemoglobin \< 9.0 g/dl * ALT or AST \> 3 times the upper limit of normal * History of cancer within the past 5 years, excluding treated non-melanoma skin cancer (basal cell carcinoma, squamous cell carcinoma) * Other uncontrolled chronic medical condition that may interfere with a patient's ability to participate in the clinical trial * Major surgery within 4 weeks of baseline visit * Receipt of live vaccine within 8 weeks of baseline visit * Pregnant or breastfeeding individuals * Inability to comply with any of the study procedures * Individuals who are incarcerated or compulsory detained
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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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Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
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University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
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Other studies related to the condition(s) this trial covers.
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