New study tracks rare muscle disease to pave way for future treatments
Knowledge-focused
Recruiting now
This study follows 150 people with primary mitochondrial myopathy, a rare genetic muscle disease, to understand how the condition changes over time. Researchers will measure muscle function, biomarkers, and imaging to find signs of disease progression. The goal is to identify use…
Sponsor: Cristina Domínguez González • Aim: Knowledge-focused
Last updated Jun 26, 2026 18:07 UTC