Epiceram Versus Elidel for Treatment of Mild to Moderate Atopic Dermatitis

NCT ID: NCT00460083

Last Updated: 2008-02-06

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 35 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-04-30
• Study Completion Date: 2008-02-29

Brief Summary

Atopic dermatitis (AD) is a common skin disease that has increased in prevalence worldwide two- to threefold over the last 50 years. Epiceram, a newly FDA-approved medical device is a topical barrier repair cream designed to deliver special epidermal lipids to the top layers of the skin in order to correct skin barrier abnormalities found in atopic dermatitis. Epiceram does not contain corticosteroids or other conventional anti-inflammatory components and represents a novel class of skin barrier repair therapy for inflammatory skin disease.

The objective of this study is to determine whether Epiceram is a safe and effective therapy for mild to moderate atopic dermatitis and whether it may serve as an alternative to Elidel therapy.

Detailed Description

Atopic dermatitis (AD) is a common skin disease that has increased in prevalence worldwide two- to threefold over the last 50 years. Current standard of care for atopic dermatitis includes topical corticosteroids and calcineurin inhibitors, such as Elidel and Protopic. The chronic use of topical corticosteroids is limited by side effects including skin atrophy, striae, and even HPA axis suppression. The long-term effects of skin immunosuppression with calcineurin inhibitors are unknown and although not proven, a theoretical risk of skin cancer exists. Novel therapies for atopic dermatitis that avoid immunosupression are greatly needed.

Epiceram, a newly FDA-approved medical device is a topical barrier repair cream designed to deliver special epidermal lipids to the top layers of the skin in order to correct skin barrier abnormalities found in atopic dermatitis. Epiceram does not contain corticosteroids or other conventional anti-inflammatory components and represents a novel class of skin barrier repair therapy for inflammatory skin disease. The objective of this study is to determine whether Epiceram is a safe and effective therapy for mild to moderate atopic dermatitis and whether it may serve as an alternative to Elidel therapy.

Conditions

Atopic Dermatitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Elidel(r)

Group Type: ACTIVE_COMPARATOR

Elidel(R) (pimecrolimus 1%)

Intervention Type: DRUG

Epiceram(r)

Group Type: EXPERIMENTAL

EpiCeram(R) -ceramide based barrier repair cream

Intervention Type: DEVICE

Interventions

Elidel(R) (pimecrolimus 1%)

Intervention Type: DRUG

EpiCeram(R) -ceramide based barrier repair cream

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. Males or females of any race 2 - 12 years of age.

2. Diagnosis of atopic dermatitis on the basis of the criteria defined by Hanifin and Rajka (Hanifin, 1980).

3. Rajka-Langeland Severity Index score of mild to moderate (Rajka, 1989).

4. At least one antecubital or popliteal fossa must be affected at the time of enrollment to serve as a target site.

Exclusion Criteria

1. Subjects with severe AD as determined by the Rajka-Langeland Severity Index (Rajka 1989).

2. Disease severity requiring medium-potency topical steroid medication to treat their atopic dermatitis more than 1 week per month.

3. Subjects with unstable or uncontrolled medical conditions that could require intensive treatment during the course of the study.

4. Subjects who require greater than 2.0 mg/day inhaled or intranasal corticosteroids.

5. Subjects who are currently participating in or, within the past 28 days, have participated in another study using an investigational drug.

6. Subjects with a history of allergy or hypersensitivity to Epiceram, Elidel, or ingredients therein, including fragrances.

7. Active infection of any type at the start of the study.

8. Any other condition that the investigator believes would pose a significant hazard to the subject if the investigational therapy were initiated.

9. Subjects must have not used any topical or systemic therapy during the washout periods.

• Minimum Eligible Age: 2 Years
• Maximum Eligible Age: 12 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Ceragenix Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Ceragenix Pharmaceuticals Inc.

Principal Investigators

Eric Simpson, MD

Role: PRINCIPAL_INVESTIGATOR

Oregon Health and Science University

Locations

UCSD

San Diego, California, United States

OHSU

Portland, Oregon, United States

Countries

United States

Other Identifiers

CGXP - 060674/ IRB00002569

Identifier Type: -

Identifier Source: org_study_id