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
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Schweiger Derm Group Coordinator of this site? Confirm its status | East Windsor | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.