# Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN

> **NCT05499091** · NA · RECRUITING · sponsor: **University Hospital, Angers** · enrollment: 1200 (estimated)

## Conditions studied

- Rare Diseases
- Genetic Disease

## Interventions

- **PROCEDURE:** Skin biopsy, blood sample, urine sample

## Key facts

- **NCT ID:** NCT05499091
- **Lead sponsor:** University Hospital, Angers
- **Sponsor class:** OTHER_GOV
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2022-10-10
- **Primary completion:** 2042-10-10
- **Final completion:** 2045-10-10
- **Target enrollment:** 1200 (ESTIMATED)
- **Last updated:** 2025-07-18


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT05499091

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT05499091, "Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN". Retrieved via AI Analytics 2026-06-03 from https://api.ai-analytics.org/clinical/NCT05499091. Licensed CC0.

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