RecruitingPhase 2NCT07750873

A Trial of CRD-4730 in HFrEF

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy, Safety, and Tolerability of CRD-4730 in Patients With Heart Failure With Reduced Ejection Fraction (HFrEF)


Sponsor

Cardurion Pharmaceuticals, Inc.

Enrollment

525 participants

Start Date

Jul 15, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

CRD-4730 is a calcium/calmodulin-dependent protein kinase II (CaMKII) inhibitor. The CALIBRATE-HF trial is a Phase 2, global, multi-center, randomized, double-blind, parallel-group, placebo-controlled trial. The trial will evaluate the efficacy, safety, and tolerability of CRD-4730 in addition to guideline directed medical therapy in participants with heart failure with reduced ejection fraction (HFrEF). Participants will be randomized to 1 of 4 study groups and receive investigational study drug or placebo twice daily (BID) for 24 weeks of treatment.


Eligibility

Min Age: 18 YearsMax Age: 85 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called CRD-4730 and a drug called Placebo for people with heart failure with reduced ejection fraction (hfref). The study is currently recruiting participants at 2 locations. People eligible for this study include aged 18 Years to 85 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGCRD-4730

Experimental, Dose A, B and C

DRUGPlacebo

Placebo


Locations(2)

Cardurion Investigative Site

Pasadena, California, United States

Cardurion Investigative Site

Bloomfield Hills, Michigan, United States

View Full Details on ClinicalTrials.gov

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NCT07750873


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