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Search clinical trials for: Mitochondrial
Total 685 results
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Steen Hvitfeldt PoulsenCompletedTransthyretin Amyloid Cardiopathy | Mitochondrial PathologyDenmark
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Abliva ABActive, not recruitingPrimary Mitochondrial DiseaseBelgium, United Kingdom, United States, Spain, Denmark, France
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PTC TherapeuticsEnrolling by invitationFriedreich AtaxiaUnited States, Australia, Brazil, Canada, France, Germany, Italy, New Zealand, Spain
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Region StockholmKarolinska InstitutetEnrolling by invitationEpilepsy | Mitochondrial Diseases | Motor Neuron Disease | Metabolic Disease | LHON | Epilepsy in Children
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University of Colorado, DenverActive, not recruitingObesity | Bariatric Surgery Candidate | Adolescent Obesity | Hepatic SteatosisUnited States
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RTI InternationalEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsEnrolling by invitationPrimary Hyperoxaluria Type 3 | Diabetes Mellitus | Hemophilia A | Hemophilia B | Hereditary Fructose Intolerance | Cystic Fibrosis | Factor VII Deficiency | Phenylketonurias | Sickle Cell Disease | Dravet Syndrome | Duchenne Muscular Dystrophy | Prader-Willi Syndrome | Fragile X Syndrome | Chronic Granulomatous Disease and other conditionsUnited States
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PTC TherapeuticsCompletedFriedreich AtaxiaUnited States, Australia, Brazil, Canada, France, Germany, Italy, New Zealand, Spain
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Providence Health & ServicesGenentech, Inc.; Institute for Systems BiologyActive, not recruitingMultiple SclerosisUnited States
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Hoffmann-La RochePPD; Laboratory Corporation of America; Illingworth Research GroupActive, not recruitingMultiple Sclerosis | Clinically Isolated SyndromeUnited States, Spain, Switzerland, France, Germany
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Pennington Biomedical Research CenterTerminated
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PTC TherapeuticsCompletedMitochondrial Diseases | Drug Resistant Epilepsy | Leigh Disease | Leigh Syndrome | Mitochondrial Encephalopathy (MELAS) | Pontocerebellar Hypoplasia Type 6 (PCH6) | Alpers Disease | Alpers SyndromeUnited States, Spain, United Kingdom, Canada, France, Italy, Poland, Sweden, Japan
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State University of New York at BuffaloHadley Jo FoundationCompletedMitochondrial Diseases | Optic Atrophy | Neurodegenerative Disease, HereditaryUnited States
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State University of New York at BuffaloThe Callum McKeefery and Nikki Albano McKeefery Pediatric Division of Genetics...CompletedMitochondrial Diseases | Optic Atrophy | Neurodegenerative Disease, HereditaryUnited States
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Khondrion BVJulius Clinical; ProPharma Group; CertaraCompletedMitochondrial Diseases | Mitochondrial DNA tRNALeu(UUR) m.3243A<G Mutation | Maternally Inherited Diabetes and Deafness (MIDD) | Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke Like Episodes (MELAS) | Chronic Progressive External Ophthalmoplegia (CPEO)Netherlands, Denmark, United Kingdom, Germany
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Lahey ClinicVarian Medical SystemsCompletedHCC | Hepatocellular CarcinomaUnited States
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Design Therapeutics, Inc.CompletedFriedreich AtaxiaUnited States
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Celia BañulsInstituto de Salud Carlos IIIActive, not recruiting
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Children's Hospital of PhiladelphiaNational Institute of Neurological Disorders and Stroke (NINDS)Completed
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Larimar Therapeutics, Inc.CompletedFriedreich AtaxiaUnited States
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Oregon State UniversityCompletedSedentary Lifestyle | Insulin Resistance | Overweight and Obesity | Metabolic Disease | Mitochondrial MetabolismUnited States
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Ohio State UniversityActive, not recruitingHealthy AdultsUnited States
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McGill UniversityCanadian Institutes of Health Research (CIHR)CompletedMuscle Atrophy | Cognitive Function | Muscle Protein Synthesis | Insulin Sensitivity | Muscle Strength | Functional Capacity | Physical Inactivity | Mitochondrial FunctionCanada
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AdventHealth Translational Research InstituteTakeda; Sanford-Burnham Medical Research InstituteActive, not recruitingObesity | Lipid Metabolism Disorders | Disorder of Lipid Storage and Metabolism | Metabolic DisorderUnited States
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AdventHealth Translational Research InstituteAmerican Diabetes AssociationActive, not recruiting
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Argo SanteGenSight BiologicsCompleted
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Reata, a wholly owned subsidiary of BiogenAbbVie; Friedreich's Ataxia Research AllianceActive, not recruitingFriedreich AtaxiaUnited States, Australia, Austria, Italy, United Kingdom
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Reata, a wholly owned subsidiary of BiogenAbbVieCompletedMItochondrial MyopathiesUnited States, Denmark
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Vanderbilt UniversityNational Institute of General Medical Sciences (NIGMS)Completed
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Children's Hospital of PhiladelphiaEnrolling by invitation
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GenSight BiologicsCompletedLeber Hereditary Optic NeuropathyUnited States, France, Italy, United Kingdom, Germany
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RWTH Aachen UniversityAssistance Publique - Hôpitaux de ParisWithdrawnFriedreich AtaxiaSpain, Italy, Austria, Germany, United Kingdom, France
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PTC TherapeuticsNo longer available
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Columbia UniversityUniversitat Autonoma de Barcelona; Instituto de Salud Carlos III; University... and other collaboratorsActive, not recruitingThymidine Kinase 2 Deficiency | Mitochondrial DNA Depletion Syndrome 2 Myopathic TypeUnited States
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Maastricht UniversityCompleted
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Pennington Biomedical Research CenterActive, not recruitingInsulin Resistance, DiabetesUnited States
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Rivus Pharmaceuticals, Inc.Withdrawn
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Monash UniversityChildren's Hospital of Philadelphia; McGill University; University of Florida; University... and other collaboratorsActive, not recruitingFriedreich AtaxiaUnited States, Canada, Australia, Brazil, Germany
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GenSight BiologicsNo longer availableLeber Hereditary Optic Neuropathy (Optic, Atrophy, Hereditary, Leber)
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Brendon Gurd, PhDCompletedMitochondrial BiogenesisCanada
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Stealth BioTherapeutics Inc.Active, not recruitingMitochondrial Diseases | Mitochondrial Myopathies | Mitochondrial Complex I Deficiency | Mitochondrial Pathology | Mitochondrial DNA Depletion | Mitochondrial DNA Mutation | Mitochondrial DNA Deletion | Mitochondrial Metabolism DefectSpain, United States, Italy, Netherlands, Australia, Germany, Hungary, New Zealand, Norway, United Kingdom
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University of Kansas Medical CenterNational Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)CompletedMitochondrial DiseasesUnited States
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Byron LamNational Eye Institute (NEI)Active, not recruitingLeber's Hereditary Optic NeuropathyUnited States
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Instituto Nacional de Ciencias Medicas y Nutricion...Completed
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Gladwin, Mark, MDNational Institutes of Health (NIH); National Institute on Aging (NIA)CompletedSedentary Lifestyle | Frailty | AgingUnited States
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University Medical Centre LjubljanaUniversity of LjubljanaActive, not recruitingCardiac ArrestSlovenia
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PTC TherapeuticsCompletedLeigh SyndromeUnited States
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University of ArkansasThe University of Texas Health Science Center at San Antonio; Jane Botsford... and other collaboratorsActive, not recruitingAutism Spectrum Disorder | Mitochondrial Disease | Developmental Delay | AutismUnited States
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University of ArkansasArkansas Children's Hospital Research InstituteActive, not recruitingNeurodevelopmental DisordersUnited States
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University of NottinghamActive, not recruitingColorectal Cancer | Prostate CancerUnited Kingdom
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University of NottinghamActive, not recruiting