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Enstilar in Combination With Enbrel or Humira for Plaque Psoriasis

P

Psoriasis Treatment Center of Central New Jersey

Status and phase

Enrolling
Phase 4

Conditions

Psoriasis

Treatments

Drug: Enstilar 0.005%-0.064% Topical Foam

Study type

Interventional

Funder types

Other
Industry

Identifiers

Details and patient eligibility

About

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

Full 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.

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Open Label Enstilar
Experimental group
Description:
once daily for 4 weeks followed by QOD for 12 weeks for patients receiving Enbrel or Humira
Treatment:
Drug: Enstilar 0.005%-0.064% Topical Foam

Trial contacts and locations

1

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Central trial contact

Jerry Bagel, MD; Elise Nelson

Data sourced from clinicaltrials.gov

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