A Safety, Tolerability, and Biomarker Trial of VS-041 in Participants With Heart Failure With Preserved Ejection Fraction (HFpEF)
Vasa Therapeutics
Summary
A Safety, Tolerability, and Biomarker Trial of VS-041 in Participants with Heart Failure with Preserved Ejection Fraction (HFpEF)
Eligibility
- Age range
- 50+ years
- Sex
- All
- Healthy volunteers
- No
Inclusion Criteria: Participants must meet all inclusion criteria to be eligible for trial participation. 1. Males or females ≥ 50 years of age at the time of signing the informed consent. 2. Diagnosis of HFpEF as defined by European Society of Cardiology or American College of Cardiology/American Heart Association criteria 3. NYHA Functional Class II or III 4. LVEF ≥ 50% demonstrated by echocardiography (ECHO) performed at Screening with evidence of heart failure 5. Elevated NT-proBNP at Screening 6. NordicPRO-C6™ ≥ 11 ng/mL at Screening. 7. Stable dose of all concomitant HF medications for…
Interventions
- DrugVS-041
VS-041 high dose, VS-041 low dose or Placebo tablet BID
- OtherPlacebo
Placebo to match VS-041
Locations (21)
- Cardiology and Medicine ClinicLittle Rock, Arkansas
- National Institute of Clinical ResearchHuntington Beach, California
- FOMATSanta Maria, California
- Invivocure LLCVan Nuys, California
- New Generation of Medical ResearchHialeah, Florida
- Jacksonville Center for Clinical ResearchJacksonville, Florida