Enstilar in Combination With Enbrel or Humira for Plaque Psoriasis

Purpose

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

Condition

  • Psoriasis

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

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

Study Design

Phase
Phase 4
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Intervention Model Description
open label
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Open Label Enstilar
once daily for 4 weeks followed by QOD for 12 weeks for patients receiving Enbrel or Humira
  • Drug: Enstilar 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

Recruiting Locations

Psoriasis Treatment Center of Central New Jersey
East Windsor 8354649, New Jersey 5101760 08520
Contact:
Elise Nelson
609-443-4500
enelson@windsordermatology.com

More Details

Status
Recruiting
Sponsor
Psoriasis Treatment Center of Central New Jersey

Study Contact

Jerry Bagel, MD
6094434500
dreamacres1@aol.com

Detailed Description

30 subjects treated with etanercept or adalimumab for at least 24 weeks with a body surface area 2-10% and physician global assessment greater than or equal to 2 will receive Enstilar® once daily for 4 weeks followed by QOD for 12 weeks.