Deucravacitinib-TNFi Combination Therapy for Difficult-to-Control Psoriatic Disease

Overview

The purpose of this research study is to determine the effectiveness of adding deucravacitinib to the participant's current Psoriatic Arthritis (PsA) treatment to see if it improves their symptoms and quality of life. This study is exploring a new treatment approach that may help improve control of psoriatic disease by targeting different parts of the disease process. By combining therapies that work together, the goal is to offer better symptom relief with fewer or more manageable side effects than some current treatments.

Interventions

• Drug Deucravacitinib
  Drug will be administered in tablet form.
• Drug Placebo
  Drug will be administered in tablet form.

Primary outcome measures

• Proportion of patients achieving a novel composite endpoint of BSA </= 1 AND SJC </= 1) OR (BSA </= 1 AND TJC </= 1) at 24 weeks [Time frame: 24 weeks]

Secondary outcome measures (12)

• Safety and tolerability, measured through adverse event reporting at baseline and weeks 5, 12, 24, and 48. [Time frame: baseline and weeks 5, 12, 24, and 48]
• Proportion of patients achieving Minimal Disease Activity (5/7 criteria) at weeks 24 and 48 [Time frame: weeks 24 and 48]
• Proportion of patients achieving Very Low Disease Activity (7/7 criteria) at weeks 24 and 48 [Time frame: weeks 24 and 48]
• Proportion of patients achieving Minimal Disease Activity - Skin (MDA with skin domain met) at weeks 24 and 48 [Time frame: weeks 24 and 48]
• Percentage achieving Psoriatic Area and Severity Index 75/90/100, PASI < 1 BL at weeks 12, 24 and 48 [Time frame: baseline and weeks 12, 24 and 48]
• Percentage achieving BSA < 1% (NPF definition) BL at weeks 12, 24 and 48 [Time frame: baseline and weeks 12, 24 and 48]
• Resolution of Spondyloarthritis Research Consortium of Canada at baseline and at weeks 24 and 48 [Time frame: baseline and weeks 24 and 48]
• Resolution of Leeds Enthesitis Index at baseline and at weeks 24 and 48 [Time frame: baseline and weeks 24 and 48]
• Change from baseline Health Assessment Questionnaire - Disability Index at weeks 24 and 48 [Time frame: baseline and weeks 24 and 48]
• Change from baseline Pruritis Numeric Rating Scale at weeks 12, 24 and 48 [Time frame: baseline and weeks 12, 24 and 48]
• Change from baseline Joint pain Visual Analog Scale at weeks 12, 24 and 48 [Time frame: baseline and weeks 12, 24 and 48]
• Change from baseline patient global assessment of arthritis at weeks 12, 24 and 48 [Time frame: baseline and weeks 12, 24 and 48]

Eligibility criteria

Inclusion criteria

• Adults aged 18-65 with confirmed psoriatic arthritis based on CASPAR criteria.

• Ability to provide informed consent and comply with study procedures.
• Patients with plaque psoriasis BSA>3% OR PsA with \[SJC>2 AND TJC >3\] despite stable background anti-TNF therapy for at least 6 months, with or without csDMARDs (i.e MTX, leflunomide, sulfasalazine, hydroxychloroquine).
• Concurrent use of 1 csDMARD, and/or NSAID, and/or oral glucocorticoid is permitted but not required during the study. If such treatment was administered, then participants must meet the following requirements:

• If on csDMARD (methotrexate \[MTX\], sulfasalazine \[SSZ\], leflunomide \[LEF\], hydroxychloroquine \[HCQ\]), the participant must have been on it for at least 12 weeks and be on a stable dose for at least 28 days prior to Day 1.

• If on MTX, the route of administration and dose must be stable and the dose must be ≤ 25 mg/week.
• If on SSZ, the dose must be ≤ 3 g/day.
• If on HCQ, the dose must be ≤ 400 mg/day.
• If on LEF, the dose must be ≤ 20 mg/day. Note: If currently not on MTX, SSZ, or HCQ, the participant must not have received it for at least 28 days prior to Day 1. If currently not on LEF, the participant must not have received it for at least 12 weeks prior to Day 1.
• If on an NSAID, the participant must be on a stable dose for at least 14 days prior to Day 1.
• Stable background use of prednisone 15 mg daily or equivalent is permitted. If on oral glucocorticoids, the participant must be on a stable dose of ≤ 15 mg/day prednisone equivalent for at least 28 days prior to Day 1.
• Note: If currently not on oral glucocorticoids, the participant must not have received oral glucocorticoids within 28 days prior to Day 1

Exclusion criteria

• History of failure of more than two anti-TNF therapies, prior history of failure of TYK2 and JAK inhibitors.

• History of prior allergic reaction or intolerance to deucravacitinib.
• History of primary failure of anti-IL17, anti-IL23 is excluded. Note that prior exposure to these agents is allowed for reasons other than primary failure, eg intolerance, insurance / access issues, etc).

• Systemic agents other than anti-TNF or csDMARD (ie. MTX, leflunomide, sulfasalazine, hydroxychloroquine) must have ceased > 6 months prior to baseline.
• Doses or glucocorticoids >15mg daily prednisone or equivalent.
• Severe cardiovascular, hepatic, or renal impairment.
• History or evidence of outpatient active infection and/or febrile illness within 14 days prior to Day 1.
• History of serious bacterial, fungal, or viral infection requiring hospitalization or parenteral antimicrobial treatment (eg, antibiotics antiviral, antifungal, or antiparasitic agents) within 60 days prior to Day 1.
• Receipt of any therapy for chronic infection (eg, pneumocystis, herpes zoster, cytomegalovirus, invasive bacterial or fungal infections, or atypical mycobacteria) at screening.
• Recent herpes zoster or herpes simplex infection or history of serious herpes zoster or herpes simplex infection defined as:
• a) Herpes zoster or herpes simplex lesions within 30 days prior to randomization, OR
• b) History of serious herpes zoster or serious herpes simplex infection, which includes, but it is not limited to, any episode of disseminated herpes simplex, multi- dermatomal herpes zoster, herpes encephalitis, ophthalmologic herpes, and/or recurrent herpes zoster (recurrent herpes zoster is defined as more than 2 episodes in the last 2 years).
• Any history of known or suspected congenital or acquired immunodeficiency state or condition that would compromise the participant's immune status (eg, history of opportunistic infections \[eg, Pneumocystis jirovecii pneumonia, histoplasmosis, or coccidioidomycosis\], history of splenectomy, primary immunodeficiency).
• Receipt of any live vaccine within 60 days prior to Day 1 or plans to receive a live vaccine during the study or within 60 days after completing study treatment.
• Evidence of, or positive testing for, hepatitis B virus or hepatitis C virus at screening.
• Positive testing for human immunodeficiency virus 1 or 2 by antibody testing at screening.
• History of active TB prior to the screening visit, signs or symptoms of active TB at screening, positive QuantiFERON®-TB Gold (or equivalent) test result or 2 successive indeterminate QuantiFERON®-TB Gold (or equivalent) test results at screening.
• History of chronic or recurrent infectious disease.
• History of VTE, MACE, active solid malignancy or history of malignancy <5 years, any hematologic malignancy; history of multiple serious infections requiring hospitalization in the past 5 years, history of opportunistic infection, any condition which in the opinion of the investigator would pose a safety risk or inability to assess key endpoints in the study.
• History of fibromyalgia/central sensitization, or other joint disease which in the opinion of the investigator would make musculoskeletal disease activity assessment challenging in the context of this study.
• History of other inflammatory dermatosis which in the opinion of the investigator would make skin disease activity assessment challenging in the context of this study (eg atopic, contact dermatitis, etc).
• Exclude use of topicals except for mild to mid-potency topical steroids for use only in cosmetically sensitive areas such as the face.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Randomized

Model

Parallel assignment

Masking

Double blind

Primary purpose

Treatment

Study locations

United States · 1 center

• UT Southwestern Medical Center — Dallas

Identifiers

NCT: NCT07280702 · STU-2025-0977

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗