RecruitingPhase 4NCT03827876

Enstilar in Combination With Enbrel or Humira for Plaque Psoriasis

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


Sponsor

Psoriasis Treatment Center of Central New Jersey

Enrollment

30 participants

Start Date

Jan 16, 2019

Study Type

INTERVENTIONAL

Conditions

Summary

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


Eligibility

Min Age: 18 Years

Inclusion Criteria5

  • 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 Criteria3

  • ˂2 or \>10% BSA
  • PGA \<2
  • Patient not receiving etanercept or adalimumab, or receiving etanercept or adalimumab \<24weeks

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Interventions

DRUGEnstilar 0.005%-0.064% Topical Foam

Enstilar 0.005%-0.064% Topical Foam applied once daily for 4 weeks followed by QOD for 12 weeks for patients receiving Enbrel or Humira


Locations(1)

Psoriasis Treatment Center of Central New Jersey

East Windsor, New Jersey, United States

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NCT03827876


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