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Familial steroid-resistant nephrotic syndrome with sensorineural deafness

MONDO:0013836

Also known as: coenzyme Q10 deficiency, primary, type 6, COQ10D6, coenzyme Q10 deficiency, primary, 6

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

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Broader categories

Disease (618) Nervous system disorder (217) Metabolic disease (215) Kidney disorder (202) Hereditary disease (172) Peripheral nervous system disorder (107) Neuromuscular disease (98) Peripheral neuropathy (90) Urinary system disorder (62) Inborn mitochondrial metabolism disorder (57)

Trials to join now! 31 Not yet recruiting 7 Not yet finished but already full! 10 Completed 11 Terminated 1

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