Home › Psoriasis › NCT03827876
Enstilar in Combination With Enbrel or Humira for Plaque Psoriasis
RecruitingPhase 4
An Open-Label Study Evaluating Enstilar® (Calcipotriene and Betamethasone Dipropionate) Foam, 0.005%/0.064% QD in Psoriasis Patients Being Treated With Etanercept or Adalimumab
Who can join
Ages 18 and older · All sexes
Full eligibility criteria
Inclusion Criteria: * Male or female adult ≥ 18 years of age; * Diagnosis of chronic plaque-type * Patient with 2-10% BSA * Physician Global Assessment of 2 or greater * Patient has been treated with etanercept or adalimumab for a minimum of 24 weeks Exclusion Criteria: * ˂2 or \>10% BSA * PGA \<2 * Patient not receiving etanercept or adalimumab, or receiving etanercept or adalimumab \<24weeks
About the study
4 weeks of adjunctive therapy of Enstilar® QD followed by 12 weeks QOD to patients with 2-10% BSA who are receiving etanercept or adalimumab for at least 24 weeks
What is being tested
- Enstilar 0.005%-0.064% Topical Foam (drug)
Sponsor: Psoriasis Treatment Center of Central New Jersey · Participants: 30 · Started: Jan 16, 2019
Contact the study team
- Jerry Bagel, MD · Phone: 6094434500
- Elise Nelson · Phone: 6094434500
Official record on ClinicalTrials.gov — NCT03827876
Locations in the U.S.
| New Jersey | Psoriasis Treatment Center of Central New Jersey, East Windsor |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.