RecruitingNot applicableNCT05499091

Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN

Studying Rare genetic disease

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
University Hospital, Angers
Principal Investigator
Estelle COLIN, MD-PhD
escolin@chu-angers.fr
Intervention
Skin biopsy, blood sample, urine sample(procedure)
Enrollment
1200 enrolled
Eligibility
All sexes
Timeline
2022 – 2045

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05499091 on ClinicalTrials.gov

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