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Phase 2 N=3 Treatment

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

Netherton Syndrome

Enrolled (actual)
3
Serious AEs
0.0%
Results posted
Dec 2014
Primary outcome: Primary: Blood Pimecrolimus Levels — 0; 0; 0.312; 1.260 ng/mL

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Pimecrolimus 1% Cream (Drug)
Age
Pediatric, Adult · 2+ yrs
Sex
All
Sponsor
Children's Hospital of Philadelphia
Primary completion
Mar 2008

Outcome Measures

OutcomeResultp-value
PRIMARY
Blood Pimecrolimus Levels
0; 0; 0.312; 1.260; 0.625; 3.630

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.

Eligibility Criteria

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.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00208026). 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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