RecruitingNot applicableNCT06926127
Genomic Profiling of Genetic and Rare Diseases
Studying Rare genetic disease
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
- Principal Investigator
- Giovanni ScambiaFondazione Policlinico Universitario A. Gemelli, IRCCS
- Intervention
- Whole Exome Sequencing (WES)(genetic)
- Enrollment
- 1500 enrolled
- Eligibility
- 90 years · All sexes
- Timeline
- 2024 – 2030
Study locations (1)
- Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC PEDIATRIA, Rome, Lazio, Italy
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.
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