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NCT06329258CompletedPhase 4

Combination of Sotyktu and Enstilar for Plaque Psoriasis

A Single Center Study to Evaluate the Effectiveness and Safety of SOTYKTU® (Deucravacitinib) in Combination With Enstilar® for Moderate to Severe Plaque Psoriasis

Source: ClinicalTrials.gov · Last updated 25 Mar 2024

Brief summary (registry, in English)

combination deucravacitinib and enstilar foam

Status (registry)
Completed
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
30 (actual)
First submitted
14 Mar 2024
Start date
6 Dec 2022
Primary completion date
13 Nov 2023
Lead sponsor
Psoriasis Treatment Center of Central New Jersey
Diseases
Psoriasis
NCT number
NCT06329258

What you commit to

  • Study type: Interventional · Phase 4
  • Participants enrolled: 30
  • From 6 Dec 2022 to the primary completion date, 13 Nov 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Forms of psoriasis other than chronic plaque-type (e.g., Pustular erythrodermic and/or guttate psoriasis) or drug induced psoriasis
  • Use of oral systemic medications or PUVA phototherapy for the treatment of psoriasis within 4 weeks (includes, but not limited to, oral corticosteroids, methotrexate, acitretin and cyclosporine).
  • Prior use of biologics within the following periods:
    • Etanercept - 4 weeks
    • Adalimumab or certolizumab pegol - 8 weeks
    • IL-17 antagonists - 16 weeks
    • Ustekinumab or IL-23 pathway inhibitors - 24 weeks
    • Other biologics - 5 half-lives
  • Patient used topical therapies or UVB phototherapy to treat psoriasis within 2 weeks of the Baseline Visit (includes, but not limited to, topical corticosteroids, vitamin D analogs, or retinoids).

Other illness

  • Other than psoriasis, any clinically significant (as determined by the investigator) cardiac, endocrinologic, pulmonary, neurologic, psychiatric, hepatic, renal, hematologic, immunologic disease, or other major disease that is uncontrolled.

Who the study is looking for

  • Male or female adult ≥ 18 years of age;
  • Diagnosis of chronic plaque-type psoriasis
  • Moderate to severe plaque type psoriasis as defined at baseline by:
    • BSA affected by plaque-type psoriasis of 10% or greater
    • PGA score of 3 or greater
    • PASI ≥ 12.
  • Able and willing to give written informed consent prior to performance of any study-related procedures Must be in general good health (except for disease under study) as judged by the Investigator, based on medical history, physical examination, clinical laboratories, and urinalysis.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Schweiger Derm Group
Coordinator of this site? Confirm its status
East WindsorUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.