Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

ACTIVE NOT RECRUITING Phase 2

Evaluate Efficacy, Safety and Tolerability of JTT-861 in Subjects With Heart Failure With Reduced Ejection Fraction

NCT06017609 · View on ClinicalTrials.gov ↗

Study Summary

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.

Conditions Studied

Interventions

  • DRUG Placebo Capsules
  • DRUG JTT-861 Capsules

Study Locations (20)

Florida

  • Nature Coast Clinical Research — Crystal River
  • Indago Research & Health Center, Inc. — Hialeah
  • Med Research of Florida — Miami
  • Pharma Medical Innovation, Inc. — Miami Lakes
  • Floridian Clinical Research — Miami Lakes

Texas

  • NextStage Clinical Research-Beaumont- (01) — Beaumont
  • Cypress Heart and Vascular Center — Cypress
  • NextStage Clinical Research-Port Arthur-(02) — Port Arthur
  • Sherman Clinical Research — Sherman
  • Waco Cardiology Associates - NextStage Clinical Research — Waco

Michigan

  • Henry Ford Hospital — Detroit
  • Profound Research LLC — Farmington Hills

Arizona

  • Arensia Exploratory Medicine Inc. — Phoenix

Illinois

  • Affinity Health — Park Ridge

Indiana

  • ASHA Clinical Research-Munster, LLC — Hammond

Louisiana

  • Monroe Research, LLC — West Monroe

Missouri

  • NextStage Clinical Research - (Kansas City [01]) — Kansas City

Trial Details

FieldValue
Enrollment Target 314 participants
Start Date 2023-12-20
Est. Completion 2026-12
Phase Phase 2

Sponsor

Akros Pharma

5 total trials

Interested in This Trial?

Always speak with your doctor before enrolling in a clinical trial.

Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06017609

The ClinicalTrials.gov registry entry for NCT06017609 describes a study currently listed as active not 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 314 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Akros Pharma, which has 5 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 Chronic Heart Failure appearing as the primary indexed condition, and to 2 interventions — of which Placebo Capsules 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: NCT06017609 reports 20 study locations spanning 11 distinct geographic areas — top geographies include Florida, Texas, Michigan. 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 NCT06017609 about?

NCT06017609 is a clinical study titled "Evaluate Efficacy, Safety and Tolerability of JTT-861 in Subjects With Heart Failure With Reduced Ejection Fraction". 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.

What is the current status of trial NCT06017609?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 314 participants. The study started on 2023-12-20. Estimated completion is 2026-12.

What conditions does trial NCT06017609 study?

This clinical trial studies the following conditions: Chronic Heart Failure. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06017609?

The interventions under investigation include: Placebo Capsules (DRUG), JTT-861 Capsules (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06017609?

This trial is sponsored by Akros Pharma, which has 5 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06017609 being conducted?

This trial has 20 study locations across Arizona, Florida, Illinois, Indiana, Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial