Efficacy of KL1333 in Adult Patients With Primary Mitochondrial Disease
Sponsored by Pharming Technologies B.V.
About this study
The primary objective of the FALCON study is to evaluate the efficacy of KL1333 on selected disease manifestations of primary mitochondrial disease (PMD) following 48 weeks of treatment. This objective involves evaluating the efficacy of KL1333 versus placebo on fatigue symptoms and impacts on daily living as well as on functional lower extremity strength and endurance. Additionally, the study evaluates the safety and tolerability of KL1333.
Enrolling at this location
IU Health University Hospital
Indianapolis, Indiana
I'm interestedThis study also enrolls at 19 other locations. See all.
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Trial data sourced from ClinicalTrials.gov.