IDDEA-HF is a randomized, double-blind, placebo-controlled study to evaluate the cardiac and renal effects of daily treatment with elamipretide in patients who have been hospitalized with congestive heart failure. Up to 300 patients will be randomized within 72 hours of presentation to receive 20 mg daily elamipretide or placebo intravenously for up to seven days. The primary endpoint is change in NT-proBNP, a cardiac biomarker reflecting the level of congestion. Secondary endpoints include change in clinical status and safety and tolerability.
"IDDEA-HF is a key step in our development of therapies for common diseases of aging. These patients have failed current therapies, experiencing an episode of acute decompensation, which highlights the intense need for new options within the heart failure treatment paradigm where we believe elamipretide can have a significant impact," said Stealth Chief Executive Officer, Reenie McCarthy. "The data from this study, together with our other ongoing trials in heart failure, will help inform our projected Phase 3 heart failure program as well as our approach to other common diseases of aging for which elamipretide may have therapeutic potential."
IDDEA-HF is the third study Stealth recently initiated to evaluate elamipretide in the heart failure setting. PROGRESS-HF and RESTORE-HF are ongoing Phase 2 randomized, double-blind, placebo-controlled trials to evaluate the effects of four weeks' treatment with daily subcutaneous injections of elamipretide on left ventricular function in patients with stable heart failure with reduced ejection fraction (PROGRESS-HF) or preserved ejection fraction (RESTORE-HF).
For additional information on IDDEA-HF or elamipretide, please refer to Stealth's website and ClinicalTrials.gov.
About Heart Failure
Heart failure affects approximately 21 million people in the United States and Europe, and the incidence is anticipated to increase as the population continues to age. The disease is characterized by a reduced ability to relax and contract the heart to pump blood throughout the body. Heart failure comes in two forms, based on changes in the amount of blood the left ventricle pumps out with each contraction, known as ejection fraction. Both forms, heart failure with reduced ejection fraction and heart failure with preserved ejection fraction, are associated with mitochondrial dysfunction and the resulting lack of energy in the heart muscle. There are currently no FDA-approved treatments for heart failure with preserved ejection fraction, and only limited treatments for heart failure with reduced ejection fraction.
Stealth's lead candidate, elamipretide, is an investigational drug with the potential to modify disease by preserving energetics and restoring normal energy production in mitochondria, while decreasing oxidative stress. The energetics from mitochondria maintain healthy physiology and prevent disease. This mitochondria-targeted candidate is being developed for both rare diseases and common diseases of aging.
Stealth BioTherapeutics: Leading Mitochondrial Medicine
Stealth BioTherapeutics is a privately held biopharmaceutical company committed to bringing mitochondrial therapies to patients to treat both rare diseases and common diseases of aging. Stealth's clinical development program is focused along several core therapeutic areas, including primary mitochondrial diseases, cardio-renal diseases and ophthalmic disorders. More information regarding Stealth and its pipeline is available at StealthBT.com.
Kate Contreras, 617-520-7088
Beth DelGiacco, 212-362-1200
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SOURCE Stealth BioTherapeutics