Ectodermal Dysplasia 1, Anhidrotic clinical trials
The registry lists 20 studies for Ectodermal Dysplasia 1, Anhidrotic across 6 countries. 1 are recruiting or about to start. Per ClinicalTrials.gov, last updated 2026-10-02.
Keep track of what changes. Save the Ectodermal Dysplasia 1, Anhidrotic studies recruiting or about to start, and get an email each week — studies that open, close, add sites or post results.
Watch these studiesWho runs them
Edimer Pharmaceuticals (13) · University Hospital Erlangen (4) · Pierre Fabre Medicament (1) · Assistance Publique - Hôpitaux de Paris (1) · EspeRare Foundation (1)
Who these studies take
Of the 1 Ectodermal Dysplasia 1, Anhidrotic studies recruiting now, 1 (100%) set no upper age limit and 0 (0%) stop at 75 or younger. 0 (0%) take children under 18. 1 (100%) are for women only and 0 (0%) for men only; 0 (0%) take healthy volunteers.
| Age | Women | Men |
|---|---|---|
| 10 | 0 (0%) | 0 (0%) |
| 18 | 1 (100%) | 0 (0%) |
| 30 | 1 (100%) | 0 (0%) |
| 40 | 1 (100%) | 0 (0%) |
| 50 | 1 (100%) | 0 (0%) |
| 65 | 1 (100%) | 0 (0%) |
| 75 | 1 (100%) | 0 (0%) |
| 85 | 1 (100%) | 0 (0%) |
Across all 20 studies, recruiting or not: 50% stop at 75 or younger and 50% at 65; 85% take children; 10% are for women only and 55% for men only; 50% take healthy volunteers. From each study’s registry entry; the criteria on its page decide.
Studies
Recruiting first, then most recently updated. Showing 20 of 20. search them.
- Intraamniotic Administrations of ER004 to Male Subjects With X-linked Hypohidrotic Ectodermal DysplasiaRecruitingNCT04980638Phase 26 countries
- Characteristics and Impacts of X-linked Hypohidrotic Ectodermal Dysplasia (XLHED) in Boys: An Observational International StudyCompletedNCT070962062 countries
- Impact of Dysregulation of Core Body Temperature on Sleep in Patients With Hypohidrotic Ectodermal DysplasiaCompletedNCT05378932Not applicable1 country
- Short Term Effects and Risks of Physical Exercise in Subjects With Hypohidrotic Ectodermal DysplasiaCompletedNCT011358881 country
- Pediatric SARS-CoV-2 Infections: Course of COVID-19, Immune Responses, Complications and Long-term ConsequencesCompletedNCT047414121 country
- Extension Study of XLHED-Affected Male Subjects Treated With EDI200 in Protocol ECP-002Active, not recruitingNCT019922895 countries
- Natural History and Outcomes in X-Linked Hypohidrotic Ectodermal DysplasiaCompletedNCT020995525 countries
- Phase 2 Study to Evaluate Safety, Pharmacokinetics, Immunogenicity and Pharmacodynamics/Efficacy of EDI200 in Male Infants With X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED)CompletedNCT01775462Phase 25 countries
- Investigation of Chronic Inflammatory Processes in Male Individuals With Hypohidrotic Ectodermal DysplasiaCompletedNCT013083331 country
- A Phase 1, Open-label, Multicenter, Safety and Pharmacokinetic Study of EDI200CompletedNCT01564225Phase 11 country
- Phenotypic Properties in Individuals Affected With XLHEDCompletedNCT018717141 country
- X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Carrier Outlook Toward Reproduction SurveyCompletedNCT013988131 country
- Phenotypic and Genetic Properties in Males at Risk for X-linked Hypohidrotic Ectodermal Dysplasia: Evaluation of an Early Diagnosis Technology and Tests to Assess Nutritional StatusCompletedNCT016299401 country
- Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected By Hypohidrotic Ectodermal DysplasiaCompletedNCT011087701 country
- Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected by Hypohidrotic Ectodermal Dysplasia - ACompletedNCT012935651 country
- Evaluation of Phenotypic and Genetic Properties in Male Subjects Affected By Hypohidrotic Ectodermal Dysplasia (ECP-012)CompletedNCT016299271 country
- Male Subjects Affected By Hypohidrotic Ectodermal Dysplasia: Intrafamilial VariationCompletedNCT013867751 country
- Medical Record Review of Hypohidrotic Ectodermal Dysplasia Clinical PhenotypeCompletedNCT013983971 country
- Sweat Duct Imaging in Mother/Newborn DyadsCompletedNCT013421331 country
- Characterization of Sweat Gland Function in Patients With Recessively Inherited Hypohidrotic Ectodermal DysplasiaCompletedNCT011092901 country