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A randomized crossover trial of elamipretide in adults with primary mitochondrial myopathy.

Amel KaraaRichard HaasAmy GoldsteinJerry VockleyBruce H Cohen
Published in: Journal of cachexia, sarcopenia and muscle (2020)
Participants who received a short-course treatment of daily SC elamipretide for 4 weeks experienced a clinically meaningful change in the 6MWT, which did not achieve statistical significance as the primary endpoint of the study. Secondary endpoints were suggestive of an elamipretide treatment effect compared with placebo. Nominal statistically significant and clinically meaningful improvements were seen in patient-reported outcomes. The results of this trial provided an efficacy signal and data to support the initiation of MMPOWER-3, a 6-month long, Phase 3 treatment trial in patients with primary mitochondrial myopathy.
Keyphrases
  • patient reported outcomes
  • study protocol
  • phase iii
  • clinical trial
  • oxidative stress
  • phase ii
  • randomized controlled trial
  • machine learning
  • combination therapy
  • open label
  • electronic health record
  • muscular dystrophy