🔎 Trials Near Me

Home › Heart Failure › NCT07465653

A Safety and Tolerability Study of HJB647 in Heart Failure Participants With Reduced Ejection Fraction

RecruitingPhase 1

A Multi-center, Randomized, Participant- and Investigator- Blinded, Placebo-controlled Crossover Study to Investigate the Safety, Tolerability, and Pharmacokinetics of HJB647 in Participants With Chronic Stable Heart Failure With Reduced Ejection Fraction

Who can join

Ages 18 to 100 · All sexes

Full eligibility criteria
Inclusion Criteria:

Participants eligible for inclusion in this study must meet all of the following criteria:

* Men and women aged 18 years or older
* Stable NYHA functional class II-III
* LVEF \<50%
* NT-proBNP ≥600 pg/ml if in sinus rhythm or ≥900 pg/ml if in atrial fibrillation at screening
* On stable standard of care therapy with sacubitril/valsartan with a dose of at least 49/51 mg BID for at least 4 weeks before screening.

Exclusion Criteria:

Participants will be deemed ineligible for inclusion if they meet any of the following exclusion criteria:

* Acute decompensated heart failure within 3 months prior to screening
* SBP \<105 mmHg at screening or baseline.
* Acute coronary syndrome, stroke, transient ischemic attack, cardiac, carotid or other major cardiovascular surgery, PCI, or carotid angioplasty within the 6 months prior to screening
* Hemodynamically significant mitral and/or aortic valve disease, or any prior valve replacement, except mitral regurgitation secondary to LV dilation at screening
* eGFR \<30 ml/min/1.73m2 at screening, as measured by the CKD-EPI formula
* BMI \>40 kg/m2
* Strong CYP3A4 inhibitors or inducers, sGC activators (vericiguat), PDE5 inhibitors, and nitroglycerin products
* Women of childbearing potential

Further eligibility criteria might apply in alignment with the trial protocol.

About the study

The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of HJB647 at two different doses in participants with chronic stable heart failure with reduced or mildly reduced ejection fraction (HFrEF/HFmrEF).

What is being tested

Sponsor: Novartis Pharmaceuticals · Participants: 12 · Started: Mar 18, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07465653

Locations in the U.S.

FloridaSynergy Healthcare, Bradenton
Nature Coast Clinical Research LLC, Inverness
Jacksonville Center for Clinical, Jacksonville
Inpatient Research Clinical LLC, Miami Lakes
Flourish Research, Winter Park

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.