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Palmoplantar PustulosisPhase 4NCT05710185

Deucravacitinib for the Treatment of Palmoplantar Pustulosis

A Phase 4 study testing Deucravacitinib in people with Palmoplantar Pustulosis, run by Brigham and Women's Hospital at 2 sites in United States.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

A prospective, single-arm, open-label trial of deucravacitinib 6 mg daily in patients with PPP. All participants will receive deucravacitinib 6 mg daily for 24 weeks, with study visits every 4 weeks. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Palmoplantar Pustulosis
What is being tested?
Deucravacitinib
Could I receive a placebo?
No, everyone receives an active treatment
How many people
3 participants
Where
2 sitesUnited States
Study dates
1 Jul 2023to 31 Jan 2025
Phase
Phase 4
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • • 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

Who cannot join

  • • 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
Show all 25Show fewer
  • 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

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • Brigham and Women's Hospital

    Boston, Massachusetts, 02115

  • University of Pennsylvania

    Philadelphia, Pennsylvania, 19104

Other trials in United States

About this study

A prospective, single-arm, open-label trial of deucravacitinib 6 mg daily in patients with PPP. All participants will receive deucravacitinib 6 mg daily for 24 weeks, with study visits every 4 weeks.

Read the detailed description

Objectives:

  1. Evaluate the efficacy of deucravacitinib in adults with PPP
  2. Evaluate the impact of deucravacitinib on quality of life in adults with PPP
  3. Evaluate the safety of deucravacitinib Primary Endpoint: • Proportion of participants who achieve a ppPASI-50 response, or at least 50% improvement in ppPASI score, at 16 weeks Secondary Endpoints: • Proportion of participants who achieve at least 50% improvement in the palmoplantar pustular psoriasis area and severity index (ppPASI-50) at 24 weeks
  • Frequency of participants with adverse events
  • Change from baseline in the Dermatology Quality of Life Index
  • Change from baseline in ppPASI
  • Percentage of patients who achieved a static Physician's Global Assessment score of 0/1
  • Change from baseline in the EQ-5D VAS score
  • Change from baseline in itch VAS
  • Change from baseline in pain VAS 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 Sample Size: A modified Simon's two-stage design will be used to maximize the safety and efficiency of this clinical trial in an orphan disease. In the first stage, 8 patients will be accrued. If 2 or fewer patients achieve a ppPASI-50 in these 8 patients, the study will be stopped. Otherwise, 10 additional patients will be accrued for a total of 18.

Analysis Plan: Descriptive statistics will be used to characterize the study population, including demographics, disease characteristics and previous treatments. For the primary outcome, the percentage of participants who achieve a ppPASI-50 response, or at least 50% improvement in ppPASI score, at 16 weeks, the response rate with a 95% CI will be calculated. For all secondary endpoints, summary and descriptive statistics will be used as appropriate , including number of observations, calculation of mean/median, standard deviation range and 95% confidence intervals.

Being tested
Deucravacitinib
Medical subject headings
Psoriasis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • DeucravacitinibDrug

    See arm/group description

Study groups in NCT05710185
Study groupRoleWhat they receive
Subjects with Palmoplantar pustulosisExperimentalAll participants will receive deucravacitinib 6 mg daily for 24 weeks, with study visits every 4 weeks.
Receives: Drug: Deucravacitinib

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proportion of Participants Who Achieve a ppPASI-50 Response, or at Least 50% Improvement in ppPASI Score

    The ppPASI is the most commonly used disease severity measure use in palmoplantar pustulosis clinic trials. The ppPASI is composed of subscores of erythema (E), pustules/vesicles (P), desquamation/scales (D) on the left (L) and right (R) palm (P) and sole (S) respectively. The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity

    Measured: 16 weeks

  2. Proportion of Participants Who Achieve a ppPASI-50 Response, or at Least 50% Improvement in ppPASI Score

    The ppPASI is the most commonly used disease severity measure use in palmoplantar pustulosis clinic trials. The ppPASI is composed of subscores of erythema (E), pustules/vesicles (P), desquamation/scales (D) on the left (L) and right (R) palm (P) and sole (S) respectively. The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity.

    This second Primary Outcome was added by administrative error since the study only has one Primary Outcome Measure. Hence, the outcome and results are a duplication of the outcome measure reported, and this one was left incomplete in the previous results reporting submission.

    Measured: 16 weeks

Secondary outcomes (6)
  1. Change From Baseline in the Dermatology Quality Life Index (DLQI)

    The DLQI is a dermatology-specific quality of life instrument to measure the impact of skin disease on different aspects of health-related quality of life. The questionnaire contains 10 questions, each scored on a 4-point Likert scale. The DLQI is calculated by adding the score of each question, resulting in a maximum of 30 and a minimum of 0. The higher the score, the more quality of life is impaired. A score higher than 10 indicates that the patient's life is being severely affected by their skin disease.

    Measured: Week 16, Week 24

  2. Change From Baseline in ppPASI

    The ppPASI is the most commonly used disease severity measure use in palmoplantar pustulosis clinic trials. The ppPASI is composed of subscores of erythema (E), pustules/vesicles (P), desquamation/scales (D) on the left (L) and right (R) palm (P) and sole (S) respectively. The PASI produces a numeric score that can range from 0 to 72, with higher PASI scores denoting more severe disease activity

    Measured: Week 16, Week 24

  3. Number of Patients Who Achieve a Physicians Global Assessment Score of 0 or 1

    The physician's global assessment is a widely used outcome measure that relies on physician visual assessment of disease severity. The static PGA determines psoriasis severity at a single point in time, without taking the baseline disease condition into clear (0), almost clear (1), mild (2), moderate (3), severe (4).

    Measured: Week 16, Week 24

  4. Change From Baseline in EQ-5D VAS

    The EQ-5D is a validated, reliable, and responsive instrument widely used in clinical trials where respondents rate their health in each of 5 dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety depression. EQ-5D questionnaire also includes a Visual Analog Scale (VAS), by which respondents can report their perceived health status with a grade ranging from 0 (the worst possible health status) to 100 (the best possible health status).

    Measured: Week 16, Week 24

  5. Change From Baseline in the Itch Visual Analogue Scale (Itch-VAS)

    The VAS-itch is a 10 cm line on which patients mark their pruritus intensity on a scale from "no itch" (0 points) to "worst imaginable itch" (100 points). The VAS-itch can be interpreted as 0 - < 30 points represents mild pruritus, ≥ 30 - 70 points moderate pruritus, ≥ 70 - 90 points severe pruritus, and ≥ 90 points severe pruritus

    Measured: Week 16, Week 24

  6. Change From Baseline in the Pain Visual Analogue Scale (Pain-VAS)

    The VAS-pain is a 10 cm line on which patients mark their pain on a scale from "no no" (0 points) to "worst imaginable pain" (100 points). The following cut points on the pain VAS have been recommended pain: no pain (0-4 mm), mild pain (5-44 mm), moderate pain (45-74 mm), and severe pain (75 - 100 mm)

    Measured: Week 16, 24

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Feb 2023
  2. Study start1 Jul 2023
  3. Primary completion1 Dec 2024
  4. Study completion31 Jan 2025

Why it stopped: Sponsor terminated funding

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
3 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05710185
Sponsor's protocol ID
2023P000194
Status last verified
Mar 2026
First submitted
24 Jan 2023
Last updated
7 Apr 2026
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Deucravacitinib in people with Palmoplantar Pustulosis, run by Brigham and Women's Hospital at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 25 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 7 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 16 Dec 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proportion of Participants Who Achieve a ppPASI-50 Response, or at Least 50% Improvement in ppPASI Score (time frame: 16 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Apr 2026.

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