Search clinical trials for: KH176

Total 6 results

  • Khondrion BV
    Julius Clinical; ProPharma Group; Europees Fonds voor Regionale Ontwikkeling... and other collaborators
    Recruiting
    Mitochondrial Diseases | MELAS | Mitochondrial DNA tRNALeu(UUR) m.3243A<G Mutation | Subacute Necrotizing Encephalomyelopathy
    Netherlands
  • Khondrion BV
    Drug Research Unit Ghent, Belgium
    Completed
    Mitochondrial Disease | MELAS | Leigh Syndrome | LHON | Mitochondrial DNA tRNALeu(UUR) m.3243A<G Mutation
    Belgium
  • Khondrion BV
    Radboud University Medical Center
    Completed
    Mitochondrial Diseases | Mitochondrial Myopathies | MELAS | Mitochondrial Encephalomyopathies | MIDD
    Netherlands
  • Khondrion BV
    Julius Clinical; ProPharma Group; Certara
    Completed
    Mitochondrial 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
  • Khondrion BV
    Julius Clinical
    Completed
    Mitochondrial Diseases | Mitochondrial Myopathies | MELAS Syndrome | Mitochondrial Encephalomyopathies | MIDD
    Netherlands, Denmark, Germany, United Kingdom
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