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Mitochondrial complex III deficiency, nuclear type 10

MONDO:0032909

Any mitochondrial complex deficiency in which the cause of the disease is a mutation in the UQCRFS1 gene.

Also known as: MC3DN10, MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 10

13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex III deficiency, nuclear type 10 itself.

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↑ Mitochondrial complex III deficiency, nuclear type (0)

Including sub-types (13) Tagged with Mitochondrial complex III deficiency, nuclear type 10 (0)

Trials to join now! 5 Not yet recruiting 1 Not yet finished but already full! 4 Completed 2 Terminated 1

New drug aims to tame hard-to-control seizures in rare mitochondrial disorders

Disease control Stopped early

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 2/3 • Sponsor: PTC Therapeutics • Aim: Disease control

Last updated Jun 27, 2026 12:03 UTC