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Clinical trial condition

Genetic Diseases, Inborn

Explore clinical trials studying Genetic Diseases, Inborn. Study availability and eligibility vary by location and protocol.

12,619 public trials 2,162 recruiting studies
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Genetic Diseases, Inborn trial results

Completed

Pegzilarginase in Subjects <24 Months Old With Arginase 1 Deficiency

NCT06582524

Conditions
Amino Acid Metabolism, Inborn Errors, Arginase 1 Deficiency, Brain Diseases, +11 more
Locations
  • Univ. Klinik für Kinder- und Jugendheilkunde Medizinische Universität Graz, Austria
  • Unidade de Doenças Metabólicas Pediatria, Hospital Santa Maria Lisbon, Portugal
  • Bradford Royal Infirmary Duckworth Lane Bradford, United Kingdom
View Trial Details
Completed

Ecopipam Treatment of Tourette's Syndrome in Subjects 7-17 Years

NCT02102698

Conditions
Basal Ganglia Diseases, Brain Diseases, Central Nervous System Diseases, +11 more
Locations
  • UCLA Los Angeles, California, United States
  • University of South Florida/Rothman Center for Neuropsychiatry St. Petersburg, Florida, United States
  • Emory University School Of Medicine Atlanta, Georgia, United States
  • University of Chicago Medical School Chicago, Illinois, United States
View Trial Details
Completed

Open Label Extension of 2 mg/kg Pegunigalsidase Alfa (PRX-102) Every 4 Weeks in Adult Fabry Disease Patients

NCT03614234

Conditions
Brain Diseases, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, +29 more
Locations
  • UAB Medicine Birmingham, Alabama, United States
  • Emory University School of Medicine Atlanta, Georgia, United States
  • University of Iowa Hospitals and Clinica Iowa City, Iowa, United States
  • Infusion Associates Grand Rapids, Michigan, United States
View all 14 locations
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