Stealth BioTherapeutics announced the initiation of MMPOWER-3, a Phase 3 study evaluating the efficacy and safety of daily subcutaneous injections of elamipretide in patients with primary mitochondrial myopathy (PMM). MMPOWER-3 will enroll eligible patients who previously participated in RePOWER, an ongoing, prospective, non-interventional study evaluating patients with PMM.
"There are no FDA-approved treatments for people with primary mitochondrial myopathy, leaving clinicians with limited options, such as vitamin regimens and palliative care, to treat the debilitating muscle weakness and fatigue that affect a patient's ability to perform everyday tasks," said Dr. Bruce H. Cohen, Director of the NeuroDevelopmental Science Center at Akron Children's Hospital. "The encouraging results from two prior Phase 2 clinical trials with elamipretide in this population make us optimistic about this investigational compound's potential to treat patients with PMM."
MMPOWER-3 is a randomized, double-blind, parallel-group, placebo-controlled trial to evaluate the effect of elamipretide in approximately 200 patients with PMM between the ages of 16 and 80. It will be followed by an open-label extension period. The trial will be conducted at 30 clinical sites across North America, Europe and Australia. The primary endpoints will be change in the distance walked during the six-minute walk test and change in the Total Fatigue score on the Primary Mitochondrial Myopathy Symptom Assessment (PMMSA), a patient-reported outcome measure. Secondary endpoints include safety, tolerability, and additional patient- and clinician-reported outcomes.
In June 2016, Stealth announced results from MMPOWER, its initial Phase 2 clinical trial studying elamipretide in PMM. In June 2017, Stealth announced results from MMPOWER-2, a Phase 2 continuation trial evaluating elamipretide's safety, tolerability and efficacy for patients with PMM, which showed evidence of effectiveness across multiple endpoints. Findings from MMPOWER, MMPOWER-2 and RePOWER helped inform the Phase 3 trial design and patient population.
MMPOWER-3 is a Phase 3, randomized, double-blind, parallel-group, placebo-controlled trial to evaluate the efficacy and safety of daily subcutaneous injections of elamipretide followed by an open-label treatment extension in subjects with PMM. Subjects will have been previously enrolled in RePOWER, which is still recruiting. The trial will assess approximately 200 patients between the ages of 16 and 80 with confirmed PMM.