Deucravacitinib for the Treatment of Palmoplantar Pustulosis

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.

Study Overview

• Status: Recruiting
• Conditions: Palmoplantar Pustulosis
• Intervention / Treatment: Drug: Deucravacitinib

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.

• Study Type: Interventional
• Enrollment (Estimated): 18
• Phase: Phase 4

Contacts and Locations

• Study Contact: Name: Liset Chacin; Phone Number: 6172645926; Email: lchacin@bwh.harvard.edu
• Study Contact Backup: Name: Alex Gionfriddo; Email: agionfriddo@bwh.harvard.edu

Study Locations

• United States
  • Massachusetts
    • Boston, Massachusetts, United States, 02115
      • Recruiting
      • Brigham and Women's Hospital
      • Contact: Liset Chacin, BS; Phone Number: 617-264-5926; Email: lchacin@bwh.harvard.edu
      • Contact: Mary O'Donnell; Email: MODONNELL6@mgh.harvard.edu
  • Pennsylvania
    • Philadelphia, Pennsylvania, United States, 19104
      • Recruiting
      • University of Pennsylvania
      • Contact: Maryte Papadopoulos; Phone Number: 215-662-2408; Email: maryte@pennmedicine.upenn.edu
      • Contact: Jennifer Mason; Email: Jennifer.Mason1@Pennmedicine.upenn.edu
      • Principal Investigator: Joel Gelfand, MD, MSCE

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

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

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Subjects with Palmoplantar pustulosis; All participants will receive deucravacitinib 6 mg daily for 24 weeks, with study visits every 4 weeks.	Drug: Deucravacitinib; See arm/group description

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
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	16 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
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	Week 24
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.	Week 16, Week 24
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	Week 16, Week 24
Percentage of patient 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).	Week 16, Week 24
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).	Week 16, Week 24
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" (10 points). The VAS-itch can be interpreted as 0 - < 3 points represents mild pruritus, ≥ 3 - 7 points moderate pruritus, ≥ 7 - 9 points severe pruritus, and ≥ 9 points severe pruritus	Week 16, Week 24
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)	Week 16, 24

Collaborators and Investigators

• Sponsor: Brigham and Women's Hospital
• Collaborators: University of Pennsylvania

Study record dates

Study Major Dates

• Study Start (Actual): July 1, 2023
• Primary Completion (Estimated): December 1, 2025
• Study Completion (Estimated): June 1, 2026

Study Registration Dates

• First Submitted: January 24, 2023
• First Submitted That Met QC Criteria: February 1, 2023
• First Posted (Actual): February 2, 2023

Study Record Updates

• Last Update Posted (Actual): November 29, 2023
• Last Update Submitted That Met QC Criteria: November 28, 2023
• Last Verified: November 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Skin Diseases; Skin Diseases, Papulosquamous; Psoriasis; Molecular Mechanisms of Pharmacological Action; Enzyme Inhibitors; Dermatologic Agents; Protein Kinase Inhibitors; Deucravacitinib
• Other Study ID Numbers: 2023P000194

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No