Enrolling by invitationNCT05236595
Research for Individualized Therapeutics in Rare Genetic Disease
Studying Rare genetic disease
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Mayo Clinic
- Principal Investigator
- Margot A Cousin, Ph.D.Mayo Clinic
- Intervention
- Individualized drug matching per genetic disease(other)
- Enrollment
- 50 target
- Eligibility
- All sexes
- Timeline
- 2021 – 2026
Study locations (3)
- Mayo Clinic in Arizona, Scottsdale, Arizona, United States
- Mayo Clinic Florida, Jacksonville, Florida, United States
- Mayo Clinic Rochester, Minneota, Minnesota, United States
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 NCT05236595 on ClinicalTrials.govOther trials for Rare genetic disease
Additional recruiting or active studies for the same condition.
- RECRUITINGNANCT06926127Genomic Profiling of Genetic and Rare DiseasesFondazione Policlinico Universitario Agostino Gemelli IRCCS
- RECRUITINGNCT06796751PREcision Diagnostics in Rare genetIC Diseases and Tumors - Long Read SequencingIRCCS Azienda Ospedaliero-Universitaria di Bologna
- ACTIVE NOT RECRUITINGPHASE1, PHASE2NCT06314490Personalized Antisense Oligonucleotide Therapy for Rare Pediatric Genetic Disease: SCN2AUniversity of California, San Diego
- ACTIVE NOT RECRUITINGNANCT05064241Overcoming Barriers to Accessing Genetic MedicineBoston Children's Hospital
- RECRUITINGNANCT05499091Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGINUniversity Hospital, Angers
- RECRUITINGNCT04586075UW Undiagnosed Genetic Diseases ProgramUniversity of Wisconsin, Madison
- RECRUITINGNCT03967743Application of a Systematic Developmental Assessment to a Novel Population: Infants With Rare Genetic DisordersBoston Children's Hospital
- RECRUITINGNCT02450851Clinical and Genetic Evaluation of Individuals With Undiagnosed Disorders Through the Undiagnosed Diseases NetworkNational Human Genome Research Institute (NHGRI)