Monroe Research, LLC | West Monroe, LA
Status and phase
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This study will evaluate the efficacy, safety, tolerability and pharmacokinetics of JTT-861 administered once daily for 12 weeks in subjects with heart failure with reduced ejection fraction (HFrEF) who are on a stable, guideline-directed medical therapy for heart failure.
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Primary purpose
Allocation
Interventional model
Masking
300 participants in 3 patient groups
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Central trial contact
Takanori Nemoto, M.S.; Kala Patel, R.Ph., RAC
Data sourced from clinicaltrials.gov
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