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AMBER-HFpEF: Assessment of CK-4021586 in a Multi-Center, Blinded Evaluation of Safety and Tolerability Results in HFpEF
NCT06793371 · View on ClinicalTrials.gov ↗
Study Summary
This is a Phase 2 dose-finding study in adult participants with symptomatic HFpEF.
Conditions Studied
Interventions
- DRUG CK-4021586 (150 mg, 300 mg, 450 mg, and 600 mg)
- DRUG Placebo to match CK-4021586
Study Locations (20)
California
- BioSolutions Clinical Research Center — Imperial
- Profound Research LLC — Pasadena
- University of California, San Francisco - Heart and Vascular Center — San Francisco
- FOMAT - Comprehensive Cardiovascular Care — Santa Maria
- Blue Coast Research Center, LLC — Vista
Florida
- New Generation of Medical Research — Hialeah
- Cleveland Clinic Florida — Weston
Alabama
- Eastern Shore Research Institute, LLC — Fairhope
Arizona
- University of Arizona Sarver Heart Center — Tucson
Arkansas
- John L. McClellan Memorial Veterans Hospital — Little Rock
Illinois
- Methodist Medical Center of Illinois — Peoria
Louisiana
- Louisiana Heart Center — Slidell
Massachusetts
- Massachusetts General Hospital — Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2025-02-06 |
| Est. Completion | 2026-09 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06793371
The ClinicalTrials.gov registry entry for NCT06793371 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cytokinetics, which has 7 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Symptomatic Heart Failure With Preserved Ejection Fraction (HFpEF) appearing as the primary indexed condition, and to 2 interventions — of which CK-4021586 (150 mg, 300 mg, 450 mg, and 600 mg) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06793371 reports 20 study locations spanning 15 distinct geographic areas — top geographies include California, Florida, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06793371 about?
NCT06793371 is a clinical study titled "AMBER-HFpEF: Assessment of CK-4021586 in a Multi-Center, Blinded Evaluation of Safety and Tolerability Results in HFpEF". This is a Phase 2 dose-finding study in adult participants with symptomatic HFpEF.
What is the current status of trial NCT06793371?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2025-02-06. Estimated completion is 2026-09.
What conditions does trial NCT06793371 study?
This clinical trial studies the following conditions: Symptomatic Heart Failure With Preserved Ejection Fraction (HFpEF). These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06793371?
The interventions under investigation include: CK-4021586 (150 mg, 300 mg, 450 mg, and 600 mg) (DRUG), Placebo to match CK-4021586 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06793371?
This trial is sponsored by Cytokinetics, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06793371 being conducted?
This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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