Efficacy and Safety of Elamipretide in Individuals With Primary Mitochondrial Myopathy
Amel Karaa, Enrico Bertini, Valério Carelli, Bruce H. Cohen, Gregory M. Enns, Marni J. Falk, Amy B. Goldstein, Gráinne S. Gorman, Richard Haas, Michio Hirano, Thomas Klopstock, Mary Kay Koenig, Cornelia Kornblum, Costanza Lamperti, Anna Lehman, Nicola Longo, Mária Judit Molnár, Sumit Parikh, H. Phan, Robert D. S. Pitceathly, Russell P. Saneto, Fernando Scaglia, Serenella Servidei, Mark A. Tarnopolsky, António Toscano, Johan L.K. Van Hove, John Vissing, Jerry Vockley, Jeffrey S. Finman, David A. Brown, James A. Shiffer, Michelango Mancuso, for the MMPOWER-3 Trial Investigators, for the MMPOWER-3 Trial Investigators, Valentino Maria Lucia, P. Alessandro, Sancricca Cristina, Grosz Zoltan, Györgyi Bathori, Daria Diodato, Gessica Vasco, Soler-Alfonso Claudia, Abdullhameed May Ali, Hanna Michael G, Enrico Bugiardini, Poole Olivia, Kendall Fran, A. Noelle Larson, Nithi Ajantha, Engelstad Kristin, Mattman Andre, M Michelle, Bischoff Alamut T, Büchner Boriana, Radelfahr Florentine, Stendel Claudia, Claudia B. Catarino, Tonni Hilary Elizabeth, Rossman Ian Tait, C. Marie, Victorio Maria Christina, Montano Vincenzo, Siciliano Gabriele, M.O. Musumeci Olimpia, Catania Alessina
Abstract
<h3>Background and Objectives:</h3> Primary Mitochondrial Myopathies (PMMs) encompass a group of genetic disorders that impair mitochondrial oxidative phosphorylation, adversely impacting physical function, exercise capacity, and quality of life (QoL). Current PMM standards-of-care address symptoms, with limited clinical impact, constituting a significant therapeutic unmet need. We present data from MMPOWER-3, a pivotal, phase-3, randomized, double-blind, placebo-controlled clinical trial that evaluated the efficacy and safety of elamipretide in participants with genetically-confirmed PMM. <h3>Methods:</h3> Following screening, eligible participants were randomized 1:1 to receive either 24weeks of elamipretide 40mg/day or placebo subcutaneously. Primary efficacy endpoints included change from baseline to Week 24 on the distance walked on the 6-minute Walk Test (6MWT), and Total Fatigue on the Primary Mitochondrial Myopathy Symptom Assessment (PMMSA). Secondary endpoints included Most Bothersome Symptom Score on the PMMSA, NeuroQoL Fatigue Short Form scores, and the Patient– and Clinician–Global Impression of PMM Symptoms. <h3>Results:</h3> Participants (N=218) were randomized (n=109 elamipretide; n=109 placebo). Mean age was 45.6 year (64% women; 94% white). The majority of participants (n=162 [74%]) had mitochondrial DNA (mtDNA) mutations, with the remainder having nuclear DNA (nDNA) defects. At screening, the most frequent bothersome PMM symptom on the PMMSA was tiredness during activities (28.9%). At baseline, mean distance walked on the 6MWT was 336.7±81.2 meters, mean score for Total Fatigue on the PMMSA was 10.6±2.5, and mean T-score for the Neuro-QoL Fatigue Short Form was 54.7±7.5. The study did not meet its primary endpoints assessing changes in the 6MWT and PMMSA Total Fatigue Score (TFS). Between the participants receiving elamipretide versus placebo, the difference in the Least Squares Mean (SE) from baseline to Week 24 on distance walked on the 6MWT was -3.2 (95% confidence interval,-18.7,12.3; <i>p</i>=0.69) meters and on the PMMSA Total Fatigue Score was -0.07 (95% confidence interval,-0.10,0.26; <i>p</i>=0.37). Elamipretide treatment was well-tolerated with most adverse events being mild to moderate in severity. <h3>Discussion:</h3> Subcutaneous elamipretide treatment did not improve outcomes in the 6MWT and PMMSA TFS in patients with PMM. However, this phase-3 study demonstrated that subcutaneous elamipretide is well-tolerated. <h3>Trial Registration Information:</h3> Trial registered with clinicaltrials.gov, Clinical Trials Identifier: NCT03323749; submitted on October 12, 2017;first patient enrolled October 9, 2017. https://clinicaltrials.gov/ct2/show/NCT03323749?term=elamipretide&draw=2&rank=9 <h3>Classification of Evidence:</h3> This study provides Class I evidence that elamipretide does not improve the 6 minute walk test or fatigue at 24 weeks compared to placebo in patients with primary mitochondrial myopathy.