Official Title: “Exploratory Safety and Systemic Absorption of Elidel (Pimecrolimus) 1% Cream for the Treatment of Netherton Syndrome”

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.

Study Type: Interventional

Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study

Study Primary Completion Date: March 2008

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.

Intervention(s) in this Clinical Trial

• Drug: Elidel (Pimecrolimus) 1% Cream
  • Open label single arm

Arms, Groups and Cohorts in this Clinical Trial

• Other: 1
  • 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 Measures

• Blood concentration of pimecrolimus
  • Time Frame: Each visit
    Safety Issue?: No
• Eczema Area and Severity Index (EASI)
  • Time Frame: Each visit
    Safety Issue?: No
• Netherton Area and Severity Assessment (NASA)
  • Time Frame: Each visit
    Safety Issue?: No
• Investigator's Global Evaluation of Disease (IGED)
  • Time Frame: Each visit
    Safety Issue?: No
• Pruritus Severity Assessment
  • Time Frame: Each visit
    Safety Issue?: No
• Transepidermal water loss
  • Time Frame: Each visit
    Safety Issue?: No

Secondary Measures

• Complete blood count with differential
  • Time Frame: Each visit
    Safety Issue?: No
• Blood electrolytes and fasting glucose
  • Time Frame: Each visit
    Safety Issue?: No
• Blood urea nitrogen and creatinine
  • Time Frame: Each visit
    Safety Issue?: No
• Liver function tests
  • Time Frame: Each visit
    Safety Issue?: No

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 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.

Gender Eligibility for this Clinical Trial: Both

Minimum Age for this Clinical Trial: 2 Years

Maximum Age for this Clinical Trial: 18 Years

Are Healthy Volunteers Accepted for this Clinical Trial?: No

Lead Sponsor: Children's Hospital of Philadelphia

Overall Clinical Trial Officials and Contacts

Albert C Yan, MD Principal Investigator Children's Hospital of Philadelphia  

Information obtained from ClinicalTrials.gov on August 29, 2008

Link to the current ClinicalTrials.gov record. http://clinicaltrials.gov/show/NCT00208026

Study ID Number: 2004-11-4063

ClinicalTrials.gov Identifier: NCT00208026

Health Authority: United States: Food and Drug Administration

Children's Hospital of Philadelphia

Foundation for Ichthyosis and Related Skin Types