# Functional Genomics of Rare Genetic Diseases: Realization of Innovative Tools With High Diagnostic Power

> **NCT04152876** · — · UNKNOWN · sponsor: **Neuromed IRCCS** · enrollment: 300 (estimated)

## Conditions studied

- Rare Diseases

## Interventions

_None listed._

## Key facts

- **NCT ID:** NCT04152876
- **Lead sponsor:** Neuromed IRCCS
- **Sponsor class:** OTHER
- **Phase:** —
- **Study type:** OBSERVATIONAL
- **Status:** UNKNOWN
- **Start date:** 2019-10-31
- **Primary completion:** 2021-07-31
- **Final completion:** 2022-07-31
- **Target enrollment:** 300 (ESTIMATED)
- **Last updated:** 2019-11-05

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04152876

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04152876, "Functional Genomics of Rare Genetic Diseases: Realization of Innovative Tools With High Diagnostic Power". Retrieved via AI Analytics 2026-06-25 from https://api.ai-analytics.org/clinical/NCT04152876. Licensed CC0.

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