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Cleidocranial Dysplasia (CCD): From Genotype to Phenotype and Considerations for Care | Clinical Trials | Clareo Health

Enrolling By InvitationNCT05368064

Cleidocranial Dysplasia (CCD): From Genotype to Phenotype and Considerations for Care

Cleidocranial Dysplasia (CCD) is a rare, autosomal dominant disorder characterized by dysplasia of bones and teeth. Given the rarity of this condition (prevalence of 1 in 1,000,000), the variable phen...

Lead sponsor: Johns Hopkins University•1 U.S. locations•View source on ClinicalTrials.gov

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Trial snapshot

StatusENROLLING_BY_INVITATION

Phase—

Enrollment300

Start dateOct 2021

Last updatedOct 22, 2025

Condition

Cleidocranial Dysostosis

Locations shown

Johns Hopkins University

Baltimore, Maryland

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: October 22, 2025Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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