- Conditions
- Acquired Immunodeficiency Syndrome, Amino Acid Metabolism, Inborn Errors, Blood-Borne Infections, +30 more
- Locations
-
- Georgetown Univ Med Ctr Washington D.C., District of Columbia, United States
Clinical trial condition
Mitochondrial Diseases
Explore clinical trials studying Mitochondrial Diseases. Study availability and eligibility vary by location and protocol.
226 public trials
38 recruiting studies
Mitochondrial Diseases trial results
Active, Not Recruiting
Characterisation of the Cognitive Profile of Patients Suffering From Friedreich's Ataxia
NCT05874388
- Conditions
- Brain Diseases, Central Nervous System Diseases, Cerebellar Diseases, +11 more
- Locations
-
- Hôpital Necker-Enfants Malades Paris, France
Active, Not Recruiting
An Open-label Extension Safety Study of MELAS Patients Who Completed TIS6463-203 (PRIZM)
NCT06961344
- Conditions
- Acid-Base Imbalance, Acidosis, Acidosis, Lactic, +23 more
- Locations
-
- UC San Diego - Altman Clinical and Translational Research Institute La Jolla, California, United States
- Children's Hospital of Colorado Aurora, Colorado, United States
- Rare Disease Research Atlanta, Georgia, United States
- Massachusetts General Hospital Boston, Massachusetts, United States
Active, Not Recruiting
Early Check: Expanded Screening in Newborns
NCT03655223
- Conditions
- 17 Alpha-Hydroxylase Deficiency, 3-Hydroxy-3-Methylglutaric Aciduria, 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency, +456 more
- Locations
-
- RTI International Research Triangle Park, North Carolina, United States
Active, Not Recruiting
A Study to Find Out How BIIB141 (Omaveloxolone) is Processed in the Body and to Learn More About Its Safety in Participants With Friedreich's Ataxia Aged 2 to 15 Years Old
NCT06054893
- Conditions
- Brain Diseases, Central Nervous System Diseases, Cerebellar Diseases, +11 more
- Locations
-
- Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States
Active, Not Recruiting
A Phase 3, Multicenter, Randomized, Double-Masked, Sham-Controlled Clinical Trial for Leber's Hereditary Optic Neuropathy (LHON) Associated With ND4 Mutation
NCT07406854
- Conditions
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, Eye Diseases, +13 more
- Locations
-
- Beijing Tongren Hospital, Capital Medical University Beijing, Beijing Municipality, China
Active, Not Recruiting
A Study to Evaluate Vitamin B3 Derivative to Treat Mitochondrial Myopathy
NCT05590468
- Conditions
- Metabolic Diseases, Mitochondrial Diseases, Mitochondrial Myopathies, +6 more
- Locations
-
- Mayo Clinic in Rochester Rochester, Minnesota, United States
Active, Not Recruiting
SAD of IVT PYC-001 in OPA1 Mutation-Associated Autosomal Dominant Optic Atrophy (Sundew)
NCT06461286
- Conditions
- Autosomal Dominant Optic Atrophy, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Cranial Nerve Diseases, +16 more
- Locations
-
- Save Sight Institute - Sydney Eye Hospital Sydney, New South Wales, Australia
- Center for Eye Research Australia (CERA) East Melbourne, Victoria, Australia
Active, Not Recruiting
Gene Therapy for Cardiomyopathy Associated With Friedreich's Ataxia
NCT05445323
- Conditions
- Brain Diseases, Cardiomyopathies, Cardiomyopathy, Secondary, +15 more
- Locations
-
- Ataxia Center and HD Center of Excellence, University of California Los Angeles, California, United States
- University of South Florida Tampa, Florida, United States
- Mayo Clinic Rochester, Minnesota, United States
Active, Not Recruiting
A Study to Assess the Safety and Efficacy of Vatiquinone in Participants With Friedreich Ataxia
NCT05515536
- Conditions
- Brain Diseases, Central Nervous System Diseases, Cerebellar Diseases, +11 more
- Locations
-
- UCLA Los Angeles, California, United States
- University of Florida Gainesville, Florida, United States
- University of South Florida Tampa, Florida, United States
- University of Iowa Iowa City, Iowa, United States
Related conditions
- Metabolic Diseases (226)
- Nutritional and Metabolic Diseases (226)
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities (211)
- Genetic Diseases, Inborn (209)
- Nervous System Diseases (176)
- Heredodegenerative Disorders, Nervous System (138)
- Central Nervous System Diseases (132)
- Neurodegenerative Diseases (132)