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Primary coenzyme Q10 deficiency 8

MONDO:0014754

Any coenzyme Q10 deficiency in which the cause of the disease is a mutation in the COQ7 gene.

Also known as: COQ10D8, COQ7 coenzyme Q10 deficiency, coenzyme Q10 deficiency caused by mutation in COQ7, coenzyme Q10 deficiency, primary, 8, coenzyme Q10 deficiency, primary, type 8

47 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Metabolic disease (215) Hereditary disease (172) Peripheral nervous system disorder (107) Neuromuscular disease (98) Peripheral neuropathy (90) Inborn mitochondrial metabolism disorder (57) Inborn errors of metabolism (42) Mitochondrial disease (39)
Trials to join now! 24 Not yet recruiting 5 Not yet finished but already full! 7 Completed 10 Terminated 1
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  • New drug aims to tame hard-to-control seizures in rare mitochondrial disorders

    Disease control Terminated

    This study tested a drug called vatiquinone in 68 people with mitochondrial disease and epilepsy that doesn't respond to standard treatments. Participants were randomly assigned to receive either vatiquinone or a placebo for 24 weeks to see if the drug could reduce the number of …

    Phase: PHASE2, PHASE3 • Sponsor: PTC Therapeutics • Aim: Disease control

    Last updated Jun 27, 2026 12:03 UTC

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