Clin2
NCT06451757Possibly a fitRecruiting

Sonlicromanol for chronic fatigue in primary mitochondrial disease

Mitochondrial DiseasesMaternally Inherited Diabetes and Deafness (MIDD)Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like Episodes (MELAS)Mitochondrial DNA tRNALeu(UUR) m.3243A<G Mutation

Part of Bones, joints & muscles, Brain & nervous system, Genetic & congenital, Heart & circulation, Hormones & metabolism clinical trials.

This trial tests a new medicine, sonlicromanol, to see if it can ease chronic fatigue and improve muscle function in people with a specific genetic condition called primary mitochondrial disease. If effective, it could offer a new treatment option to improve daily energy and quality of life.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
220 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 years or older.
  • You have a confirmed mitochondrial disease with a specific genetic change (m.3243A>G) and at least 20% of that change in your blood, urine, cheek cells, or muscle.
  • You have had fatigue for at least 3 months, and a fatigue score above a certain level at the screening visit.
  • You can stand up and sit down from a chair five times in under 30 seconds at the start of the trial.
  • You have no serious heart, lung, or digestive problems, and no recent heart procedures or heart rhythm issues that could interfere with the trial.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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