Natural History and Outcomes in X-Linked Hypohidrotic Ectodermal Dysplasia

NCT ID: NCT02099552

Last Updated: 2017-09-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-04-30

Study Completion Date

2016-12-31

Brief Summary

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The proposed natural history study will enroll male and female patients, ages 36 months and younger, who have a diagnosis of XLHED based on genetic testing and who have not received an investigational study drug. The study protocol will include collection of all relevant medical history and documentation of clinical outcomes using age-appropriate, minimally invasive technologies. Data will be collected both retrospectively, back to pregnancy assessments that may be available, and prospectively through age 5 yrs.

Detailed Description

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Important to the development and regulatory approval of therapies for XLHED will be the collection of data on the clinical history and prospective health of those affected by XLHED. The proposed natural history study will enroll male and female patients, ages 36 months and younger, who have a diagnosis of XLHED based on genetic testing and who have not received an investigational study drug. The study protocol will include collection of all relevant medical history and documentation of clinical outcomes using age-appropriate, minimally invasive technologies. Data will be collected both retrospectively, back to pregnancy assessments that may be available, and prospectively through age 5 yrs. Genotype-phenotype correlations in XLHED, based on well-documented health records and prospective assessments on genetically-confirmed individuals, may now provide new and clinically-predictive information for the benefit of patients, families, health care providers and clinical investigators designing trials for therapeutic interventions.

Conditions

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X-Linked Hypohidrotic Ectodermal Dysplasia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

OTHER

Study Groups

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XLHED

Those with the condition of XLHED

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

Subjects must meet all of the following criteria to be enrolled in this study:

1. Confirmed genetic diagnosis of XLHED
2. Written informed consent of both parents (if reasonably available)

Exclusion Criteria

Subjects who meet any of the following criteria cannot be enrolled in this study:

1. Medically-significant complications or congenital anomalies outside of those considered to be associated with the diagnosis or status of XLHED
2. Having received an investigational study drug prior to enrollment. For subjects less than 6 months of age, the mother cannot have taken an investigational drug during her pregnancy.
3. Known hypersensitivity to pilocarpine or pilocarpine-like muscarinic agonists
4. Presence of pacemakers
Maximum Eligible Age

36 Months

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Edimer Pharmaceuticals

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ramsey Johnson, MSM

Role: STUDY_DIRECTOR

Edimer Pharmaceuticals

Locations

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University of California, San Francisco

San Francisco, California, United States

Site Status

Children's National Medical Center

Washington D.C., District of Columbia, United States

Site Status

Washington University School of Medicine

St Louis, Missouri, United States

Site Status

Hôpital Necker-Enfants Malades

Paris, , France

Site Status

University Hospital Erlangen

Erlangen, Bavaria, Germany

Site Status

Azienda Ospedaliera-Polo Universitario "Luigi Sacco"

Milan, , Italy

Site Status

University Hospital of Wales

Cardiff, , United Kingdom

Site Status

Countries

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United States France Germany Italy United Kingdom

Other Identifiers

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ECP-015

Identifier Type: -

Identifier Source: org_study_id

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