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KH176 under development for rare mitochondrial disease: a first in man randomized controlled clinical trial in healthy male volunteers
BACKGROUND: Mitochondrial disorders are a clinically, biochemically and genetically heterogeneous group of multi-system diseases, with an unmet medical need for treatment. KH176 is an orally bio-available small molecule under development for the treatment of mitochondrial(−related) diseases. The com...
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| Publicado no: | Orphanet J Rare Dis |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5644106/ https://ncbi.nlm.nih.gov/pubmed/29037240 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-017-0715-0 |
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