Safety Study of Elidel (Pimecrolimus) 1% Cream to Treat Netherton Syndrome

Phase 1

Completed

Conditions: Netherton Syndrome

Interventions: Drug: Pimecrolimus 1% Cream

Registration Number: NCT00208026

Lead Sponsor: Children's Hospital of Philadelphia

Brief Summary: Netherton syndrome is a genetic condition that can result in abnormal skin functioning. People with this condition often have red and scaling skin; sparse or short hair; and problems with absorption of medicines or chemicals that are applied to the skin. If these chemicals are absorbed at a high level, they may cause health problems. Elidel (pimecrolimus) is a new medicine that is available as a cream. It has been shown to help improve the appearance of the skin in patients with another skin condition known as atopic dermatitis, and is approved by the United States (US) Food and Drug Administration for use in children with mild to moderate atopic dermatitis. The purpose of this study is to determine if Elidel is safe, to see whether the medication is absorbed through the skin, and to see if side effects are associated with its use in children with Netherton syndrome.

Detailed Description: Patients with Netherton syndrome, a rare genodermatosis, manifest a chronic, eczematous dermatitis with erythema and scaling that is often recalcitrant to conventional therapy with emollients and topical corticosteroids. These patients display an altered epidermal barrier with increased permeability to topical agents and are therefore susceptible to evaporative transepidermal water loss and infection. Topical therapy with the calcineurin inhibitors tacrolimus and pimecrolimus has been demonstrated to improve the skin integrity and the quality of life of patients with several chronic dermatoses, including atopic dermatitis. As a result of the underlying skin barrier dysfunction, however, the possibility of significant systemic absorption and resultant side effects is a concern when these agents are used in patients with Netherton syndrome. Experience with topical tacrolimus 0.1% ointment for patients with Netherton syndrome has demonstrated both marked efficacy as well as significant systemic absorption of the drug in this patient population. Use of topical pimecrolimus in patients with Netherton syndrome has not been reported to date. Investigation of the extent of systemic absorption and side effects will help to define the safety and efficacy profile of topical pimecrolimus in patients with Netherton syndrome.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 3

Inclusion Criteria

Clinical diagnosis of Netherton syndrome
Normal laboratory values within 3 months prior to enrollment
Signed written informed consent
Willingness and ability to comply with the study requirements
For women of childbearing age, negative urine pregnancy test at enrollment and then monthly thereafter; women of childbearing age who are not abstinent must use contraception.

Exclusion Criteria

Clinically significant physical examination or laboratory abnormalities
Clinical evidence of liver disease or liver injury as documented by abnormal liver function tests
Symptoms of a significant acute illness in the 30 week period preceding the start of treatment
Patients with known serious adverse reactions or hypersensitivity to macrolides or calcineurin inhibitors or with known hypersensitivity to any of the ingredients of the study medication or history of adverse reactions to the anesthetic product used for blood draws
Topical tacrolimus or Elidel within 2 weeks prior to dosing
Systemic steroid, systemic tacrolimus, or any immunosuppressant within 1 month prior to dosing
Phototherapy within 1 month prior to dosing
Use of inhibitors of Cytochrome P450 3A4 (CYP3A4) iso-enzyme within 2 weeks prior to dosing
Topical steroids or other topical therapy (except tacrolimus) may be used up to the day of 1st application of Elidel; however, treatment must be discontinued during the treatment period. Topical treatment of corticosteroids may resume immediately after the treatment period or in case an alert value has been exceeded and the Elidel treatment will be continued only on the face and neck.
Participation in any clinical trials within 2 months prior to dosing
History or clinical evidence of cardiovascular, respiratory, renal, hepatic, gastrointestinal, hematologic, neurologic disease, or any disease other than Netherton syndrome, that may put the subject at undue risk. Any surgical or medical condition which might significantly alter the absorption, distribution, metabolism or excretion of drugs.
History of presence of malignancy or lymphoproliferative disease
Presence of any viral or fungal or untreated bacterial skin infection
Known HIV positivity or active hepatitis B or C
History of immunocompromise
No vaccines containing live viruses are to be administered during the study period.

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Pimecrolimus 1% Cream	Pimecrolimus 1% Cream	Treatment with drug/Elidel. Single arm-open-label treatment arm. A Pilot Study of the Efficacy and Safety of Pimecrolimus Cream 1% for the Treatment of Netherton Syndrome:

Primary Outcome Measures

Name	Time	Method
Blood Pimecrolimus Levels	Each visit up to 18 months: Study Days 1, 7, 14, 28, 56, 84, 175, 360, and 520	At each scheduled visit, blood concentration of pimecrolimus were obtained. This value reflects the amount of pimecrolimus in the blood. This is measured directly from the blood and provides an estimate of the degree of absorption of the treatment medication through the skin into the blood.

Secondary Outcome Measures