Coenzyme Q10 deficiency
MONDO:0018151A genetically heterogeneous condition, typically inherited in an autosomal recessive fashion, characterized by coenzyme Q10 deficiency.
Also known as: CoQ10 deficiency, coenzyme Q10 deficiency disease, coenzyme Q10 deficiency, primary, CoQ10 deficiency, primary
21 clinical trials for this condition and its sub-types, 3 tagged with Coenzyme Q10 deficiency itself.
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Sub-types of Coenzyme Q10 deficiency
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Coenzyme Q10 deficiency, primary, 1 0 trials
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Coenzyme Q10 deficiency, primary, 3 0 trials
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Coenzyme q10 deficiency, primary, 9 0 trials
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Primary coenzyme Q10 deficiency 8 0 trials
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New drug aims to tame hard-to-control seizures in rare mitochondrial disorders
Disease control Stopped earlyThis 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 2/3 • Sponsor: PTC Therapeutics • Aim: Disease control
Last updated Jun 27, 2026 12:03 UTC
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Could a simple blood test track nerve damage? a study investigates NT-3 levels in neuropathy.
Knowledge-focused Stopped earlyThis study measures levels of a protein called NT-3 in the blood of people with peripheral neuropathy or Charcot-Marie-Tooth disease. Researchers will compare these levels with measures of muscle strength, mobility, and daily function. The goal is to see whether NT-3 levels corre…
Sponsor: Zarife Sahenk • Aim: Knowledge-focused
Last updated Jul 31, 2026 00:00 UTC