Deucravacitinib for the Treatment of Palmoplantar Pustulosis

Description

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.

Conditions

Palmoplantar Pustulosis

Study Overview

Study Details

Study overview

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.

Deucravacitinib for the Treatment of Palmoplantar Pustulosis

Deucravacitinib for the Treatment of Palmoplantar Pustulosis

Condition
Palmoplantar Pustulosis
Intervention / Treatment

-

Contacts and Locations

Boston

Brigham and Women's Hospital, Boston, Massachusetts, United States, 02115

Philadelphia

University of Pennsylvania, Philadelphia, Pennsylvania, United States, 19104

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility 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
  • * • 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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Brigham and Women's Hospital,

Study Record Dates

2026-06-01