Reversal of Epidermal Phenotype in Severe Atopic Dermatitis With Cyclosporine Therapy

Completed · Not applicable

Conditions studied: Atopic Dermatitis, Eczema

In brief

Atopic Dermatitis (AD) or eczema is a chronic relapsing inflammatory disease that affects 1-3% of the adults and up to 25% of the children in the United States. Patients with severe AD will be studied during a 24-week study with systemic cyclosporine (Neoral, capsule form) to evaluate the immune suppression and pathological correlation of cyclosporine A in these patients in order to determine the extent to which immune activation drives the pathological epidermal phenotype.

Key facts

Study ID

NCT01149759

Run by

Rockefeller University

People needed

9

Starts

2010-06-01

Expected to finish

2014-12-01

Last updated by the study team

2017-03-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Severe AD (defined as having a mean SCORAD score> 40,, with significant disease activity, pruritus, and sleep disturbances (13), suitable for treatment with Cyclosporine, and have failed or unsuitable for other treatment modalities, including topical and or systemic steroids or phototherapy. Patients must also have an IGA score of 3 or greater,
• Males and females age 18 and above (if females are of child-bearing potential they must agree to use acceptable contraception during the study).
• No systemic treatment contraception must commence 2 weeks prior to initiating the drug.
• No systemic treatment for 4 weeks, no topical treatment or phototherapy for 2 weeks

You may not qualify if…

• Previously treated with cyclosporine and had unacceptable toxicity
• Past or current history of malignancy (except for treated isolated skin cancers)
• Renal, hepatic, and hematologic laboratory values greater than CTC grade 1 toxicity, such as but not limited to creatinine >1.5 ULN, SGOT>2.5 ULN. Values greater then grade 1 would most likely represent clinically significant renal, hepatic or hematologic disease
• Stage I hypertension is defined as >140/90. Patients with this blood pressure or higher on two separate occasions, whether on medications or not, will be excluded (JNC guidelines www.nhlbi.nih.gov/guidelines/hypertension )
• Significant lipid panel abnormality (any grade 1 toxicity on CTC scale)
• Lactating females
• Other medical condition that would increase the risk of cyclosporine toxicity
• Positive PPD
• Primary or secondary immune deficiency (including known HIV status)
• Possible or known pregnancy
• Serious infection (such as active hepatitis)
• Drug or alcohol abuse
• Inability or lack of willingness to co-operate with regular monitoring
• Severe photodamage/precancerous skin lesions due to previous sunlight exposure, or photo/photochemotherapy
• Concurrent use of PUVA or UVB, other radiation therapy,
• Concurrent use of other immunosuppressive agents such as MTX, Immuran, Cyclophosphamide, Cellcept, etc.(because of the possibility of excessive immunosuppression and the subsequent risk of malignancies)
• Active infections, infections or history of serious infection requiring hospitalization, antibiotics, antivirals,or antifungals within 30 days of baseline
• History of other inflammatory skin conditions (such as psoriasis, pemphigus, etc.
• Patients with background skin conditions that might be directly related to atopic dermatitis (such as post inflammatory hyperpigmentation) will not be excluded as well as common background non-inflammatory skin conditions such as seborrheic keratosis, benign pigmented lesions, acne, etc

Where it is running

• The Rockefeller University — New York, New York, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.