ClinicalTrials.gov record
Active, not recruiting Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT06017609

Public ClinicalTrials.gov record NCT06017609. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 16, 2026, 2:40 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2a, Multicenter, Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Evaluate the Efficacy, Safety and Tolerability of JTT-861 Administered for 12 Weeks in Subjects With Heart Failure With Reduced Ejection Fraction

Study identification

NCT ID
NCT06017609
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Akros Pharma Inc.
Industry
Enrollment
314 participants

Conditions and interventions

Interventions

  • JTT-861 Capsules Drug
  • Placebo Capsules Drug

Drug

Eligibility (public fields only)

Age range
30 Years to 85 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 19, 2023
Primary completion
Apr 30, 2026
Completion
Nov 30, 2026
Last update posted
Feb 8, 2026

2023 – 2026

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
19
Facility City State ZIP Site status
Arensia Exploratory Medicine Inc. Phoenix Arizona 85015
Nature Coast Clinical Research Crystal River Florida 34429
Indago Research & Health Center, Inc. Hialeah Florida 33012
Med Research of Florida Miami Florida 33186
Pharma Medical Innovation, Inc. Miami Lakes Florida 33014
Floridian Clinical Research Miami Lakes Florida 33016
Affinity Health Park Ridge Illinois 60068
ASHA Clinical Research-Munster, LLC Hammond Indiana 46324
Monroe Research, LLC West Monroe Louisiana 71291
Henry Ford Hospital Detroit Michigan 48202
Profound Research LLC Farmington Hills Michigan 48334
NextStage Clinical Research - (Kansas City [01]) Kansas City Missouri 64114
Laurelton Heart Specialist P.C. Rosedale New York 11422
Capital Area Research, LLC Camp Hill Pennsylvania 17011
Onsite Clinical Solutions, LLC Rock Hill South Carolina 29732
NextStage Clinical Research-Beaumont- (01) Beaumont Texas 77702
Cypress Heart and Vascular Center Cypress Texas 77429
NextStage Clinical Research-Port Arthur-(02) Port Arthur Texas 77642
Sherman Clinical Research Sherman Texas 75092
Waco Cardiology Associates - NextStage Clinical Research Waco Texas 76712

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 55 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06017609, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 8, 2026 · Synced May 16, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06017609 live on ClinicalTrials.gov.

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