Clinical Trials on Mitochondrial Genetic Disorders
Total 151185 results
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Neurophth Therapeutics IncRecruitingLeber Hereditary Optic Neuropathy (LHON)China, United States
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Wuhan Neurophth Biotechnology Limited CompanyRecruitingLeber's Hereditary Optic Neuropathy (LHON)China
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Hôpital Necker-Enfants MaladesEuropean Georges Pompidou Hospital; CLAIROPCompletedSafety Issues | Efficacy, SelfFrance
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Edison Pharmaceuticals IncNo longer availableLeber's Hereditary Optic NeuropathyUnited States
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Medical College of WisconsinTerminatedLeber's Hereditary Optic Neuropathy (LHON)United States
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University Hospital, AngersUnknownLeber Hereditary Optic NeuropathyFrance
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GenSight BiologicsCompletedLeber Hereditary Optic NeuropathyUnited States, France, Italy, United Kingdom, Germany
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GenSight BiologicsActive, not recruitingLeber Hereditary Optic NeuropathyBelgium, Spain, United States, France, United Kingdom, Taiwan, Italy
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Santhera PharmaceuticalsCompletedLeber's Hereditary Optic Neuropathy (LHON)Italy, Germany, France, Austria, Greece, Netherlands
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GenSight BiologicsCompletedLeber Hereditary Optic NeuropathyUnited States, France, Italy, Spain, United Kingdom
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Huazhong University of Science and TechnologyShiyan Taihe HospitalActive, not recruitingLeber Hereditary Optic NeuropathyChina
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GenSight BiologicsCompletedLeber Hereditary Optic NeuropathyFrance
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Santhera PharmaceuticalsEuropean Vision Institute Clinical Research NetworkCompletedLeber Hereditary Optic Neuropathy (LHON)Belgium, France, Denmark, Italy, Slovenia
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Lev-Hasharon Mental Healtlh CenterUnknownBipolar Affective DisorderIsrael
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Shanghai Mental Health CenterRecruitingDepressive Disorder | Genetic ChangeChina
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The Champ FoundationChildren's Hospital of Philadelphia; The Cleveland ClinicRecruitingPearson Syndrome | Single Large Scale Mitochondrial DNA Deletion Syndromes (SLSMDS)United States
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Neurophth Therapeutics IncActive, not recruitingLeber Hereditary Optic Neuropathy (LHON)United States
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Santhera PharmaceuticalsCompletedLeber's Hereditary Optic Neuropathy (LHON)United States, United Kingdom, Spain, Poland, Austria, Belgium, Bulgaria, Germany, Italy, Portugal
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Santhera PharmaceuticalsCompletedLeber's Hereditary Optic Neuropathy (LHON)Belgium, Netherlands, France, Germany, Norway, United Kingdom, Italy
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Mahidol UniversityCompletedOptic Atrophy, Hereditary, LeberThailand
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Eunice Kennedy Shriver National Institute of Child...CompletedMetabolic Disease | Genetic DisorderUnited States
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Hacettepe UniversityCompletedMusculoskeletal Diseases | Genetic Disease | Metabolic Disease | Congenital Disorders | Developmental Delay DisorderTurkey
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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 WashingtonAmerican Heart AssociationCompletedHeart Failure，Congestive | Mitochondrial Alteration | Heart Failure New York Heart Association Class IVUnited States
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University of AarhusNovo Nordisk A/SEnrolling by invitationCardiac Allograft Vasculopathy | Acute Cellular Graft Rejection | Mitochondrial Function | Primary Graft FailureDenmark
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Lexeo TherapeuticsRecruitingFriedreich Ataxia | Cardiomyopathy, SecondaryUnited States, Canada
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Helix, IncMedical University of South Carolina; HealthPartners Institute; WellSpan Health; St. Luke's Hospital and Health Network, Pennsylvania and other collaboratorsRecruiting
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The University of Texas Health Science Center at...National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)RecruitingType 2 Diabetes | Non-Alcoholic Fatty Liver Disease | Mitochondrial Metabolism DisordersUnited States
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Wayne State UniversityUnknownBipolar Disorder I | Bipolar Disorder II | Bipolar Affective Disorder, Currently in RemissionUnited States
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Mendel TuchmanChildren's Hospital of Philadelphia; University of California, Los Angeles; Icahn... and other collaboratorsCompletedMethylmalonic Acidemia | Carbamoyl-Phosphate Synthase I Deficiency Disease | Propionic Acidemia, Type I and/or Type II | Ornithine Carbamoyltransferase DeficiencyUnited States
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Jose Luis Urcelay SeguraUnknownAmyotrophic Lateral SclerosisSpain
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Great Ormond Street Hospital for Children NHS Foundation...National Institute for Health Research, United Kingdom; The Freya FoundationRecruitingPyruvate Dehydrogenase Complex Deficiency | Pyruvate Dehydrogenase E1 Alpha Deficiency | Pyruvate Dehydrogenase E1-Beta Deficiency | Pyruvate Dehydrogenase E2 Deficiency | Pyruvate Dehydrogenase Phosphatase DeficiencyUnited Kingdom
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Children's Hospital of PhiladelphiaEunice Kennedy Shriver National Institute of Child Health and Human Development...WithdrawnUrea Cycle Disorders, Inborn | Inborn Errors of Metabolism | Propionic Acidemia | Methylmalonic Acidemia | Carbamyl Phosphate Synthetase Deficiency
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University of CopenhagenCompletedType 2 Diabetes | Oxidative Stress | Mitochondrial Reactive Oxygen Species ProductionDenmark
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Charite University, Berlin, GermanyGerman Federal Ministry of Education and ResearchCompleted
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University of South FloridaCompletedFriedreich's Ataxia | Spinocerebellar Ataxia - All Sub-typesUnited States
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Santhera PharmaceuticalsCompletedLeber's Hereditary Optic NeuropathyCanada, Germany, United Kingdom
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Eunice Kennedy Shriver National Institute of Child...National Institutes of Health Clinical Center (CC); National Institute of Neurological... and other collaboratorsActive, not recruitingGenetic DisorderUnited States
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Aevi Genomic Medicine, LLC, a Cerecor companyCompletedAttention Deficit Disorder With HyperactivityUnited States
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Rick HulskesPhotonics Healthcare B.V., Utrecht, The NetherlandsCompletedSurgical Site Infection | Mitochondrial Oxygenation MeasurementNetherlands
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Fondazione SISA (Societa Italiana per lo Studio...RecruitingFamilial Hypercholesterolemia | Genetic DisorderItaly
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Region StockholmKarolinska InstitutetRecruitingBipolar Disorder | Bipolar Depression | Bipolar I Disorder | Bipolar II Disorder | Bipolar Affective Disorder; Remission in | Bipolar Affective Disorder, Currently Depressed, ModerateSweden
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University of Colorado, DenverCompletedMitochondrial Diseases | Human Immunodeficiency Virus (HIV)United States
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University Hospital HeidelbergGerman Cancer Research CenterCompletedType2 Diabetes | Fatty Acid Deficiency | Alteration of Mitochondrial MembraneGermany
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International Rett Syndrome FoundationBaylor College of Medicine; Children's Hospital of Philadelphia; University of... and other collaboratorsRecruitingNervous System Diseases | Neurologic Manifestations | Neurobehavioral Manifestations | Genetic Diseases, X-Linked | Intellectual Disability | Neurodevelopmental Disorders | Neurologic Disorder | Rett Syndrome | Genetic Disease | Rett Syndrome, AtypicalUnited States
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University of Split, School of MedicineUnknownCoronary Artery Disease | Diabetes Mellitus | Mitochondrial Metabolism DisordersCroatia
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PTC TherapeuticsAxio Research. LLCCompleted
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Taysha Gene Therapies, Inc.Withdrawn
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GenSight BiologicsNo longer availableLeber Hereditary Optic Neuropathy (Optic, Atrophy, Hereditary, Leber)
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Eunice Kennedy Shriver National Institute of Child...CompletedObesity | Developmental Delay | Mental Retardation | Genetic DisorderUnited States, Canada