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Phase 2 N=16 Treatment

Apremilast for Atopic Dermatitis - A Pilot Study in Adults

Atopic Dermatitis

Enrolled (actual)
16
Serious AEs
0.0%
Results posted
Jan 2020
Primary outcome: Primary: Change in EASI Scores — -8.8; -8.2 units on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Apremilast (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Oregon Health and Science University
Primary completion
Jul 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in EASI Scores
-8.8; -8.2
SECONDARY
Number of Participants in Each IGA Category
0; 1; 2; 8; 3; 1
SECONDARY
Change in Pruritus (Visual Analog Scale) Score
-32.2; -13.4
SECONDARY
Change In DLQI Scores
-8.3; -6.3

Summary

The purpose of this study is to obtain preliminary data regarding the safety and tolerability of apremilast in AD to support the design of larger controlled studies.

Eligibility Criteria

Inclusion Criteria

  • Disease severity of Moderate, Severe, or Very Severe by Investigator Global Assessment.
  • Disease severity must be greater than or equal to 6 on the Rajka-Langeland Severity Scoring system corresponding to moderate-severe disease.
  • Baseline EASI score must be greater than or equal to 11. A previous validation study for the EASI scoring system revealed patients with moderate to very severe disease had mean EASI scores ranging from 11-30.
  • Candidate for, or previously on systemic therapy, including cyclosporine, methotrexate, or other immunosuppressant and treatment with ultraviolet light. Specifically, subjects are considered candidates for systemic therapy when their disease is not adequately controlled using topical therapies or side-effects prevent the further safe use of topical therapies.
  • Subjects must meet the washout requirements

Exclusion Criteria

  • History of active mycobacterial infection with any species (including Mycobacterium tuberculosis) within 3 years prior to screening visit. Subjects with Mycobacterium tuberculosis infection more than 3 years prior to screening visit are allowed if successful treatment was completed at least 3 years prior to randomization and is documented and available for verification.
  • At least 3 major bacterial infections resulting in hospitalization and/or requiring intravenous antibiotic treatment within the past 2 years.
  • Clinically significant abnormality on the chest X-ray (CXR) at screening. Chest X-rays performed within 3 months prior to start of study drug are acceptable.
  • Use of any investigational medication within 4 weeks prior to start of study drug or 5 pharmacokinetic/pharmacodynamic half-lives (whichever is longer).
  • Any clinically significant abnormality on 12-lead ECG (electrocardiogram) at screening.
  • History of congenital or acquired immunodeficiency (e.g., Common Variable Immunodeficiency [CVID]).
  • Hepatitis B surface antigen positive or Hepatitis B core antibody positive at screening.
  • History of Human Immunodeficiency Virus (HIV) infection.
  • Antibodies to Hepatitis C at screening.
  • History of squamous cell carcinoma of the skin and thin melanoma.
  • Systemic corticosteroid-dependent asthma.
  • Active infection of any type at the time of enrollment.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01393158). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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