A Safety, Tolerability, and Biomarker Trial of VS-041 in Participants With Heart Failure With Preserved Ejection Fraction (HFpEF)
NCT07219511 · Status: RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 42
Last updated 2026-04-09
Summary
A Safety, Tolerability, and Biomarker Trial of VS-041 in Participants with Heart Failure with Preserved Ejection Fraction (HFpEF)
Conditions
- Heart
- Heart Failure With Preserved Ejection Fraction (HFPEF)
Interventions
- DRUG
-
VS-041
VS-041 high dose, VS-041 low dose or Placebo tablet BID
- OTHER
-
Placebo
Placebo to match VS-041
Sponsors & Collaborators
-
Vasa Therapeutics
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-11-04
- Primary Completion
- 2026-06-30
- Completion
- 2026-07-31
- FDA Drug
- Yes
Countries
- United States
Study Locations
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