The KHENEREXT Study
Conditions
- 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)
Interventions
- DRUG: Oral administration of 100 mg KH176 twice daily
Sponsor
Khondrion BV
Collaborators
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