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Developing innovative therapies that bring new hope to patients with dilated cardiomyopathy (DCM) — that is the mission of CardioGenix.

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Shaping the Future of

Cardiomyopathy

立体的な心臓が中心にあり、周囲に分子構造とDNAが浮かぶ、バイオテクノロジーと心臓医療を象徴する青系の横長画像

Shaping the Future for Cardiomyopathy Care

Restoring Heart Muscle Power Through Science

CardioGenix advances precision medicine by uncovering the root causes of hereditary DCM through biotechnology, identifying compounds that mitigate its impact and pioneering new possibilities for treatment.

CardioGenix 
DCM Research Laboratory

DCM • Cardiomyopathy • Biotech • New Hope • Medical Innovation • Genome Targeted • CardioGenix

Our Founding Story

I am Sachio Morimoto, Representative of CardioGenix LLC. For many years at Kyushu University and the International University of Health and Welfare, I have researched hereditary Dilated Cardiomyopathy (DCM). Certain forms of hereditary DCM are intractable diseases that progress due to reduced cardiac calcium sensitivity.(PDF).Without fundamental cures, many patients face the severe reality of awaiting heart transplants.Our research has demonstrated that restoring myocardial calcium sensitivity is the key to treating DCM. During my academic tenure, drug screening conducted with LTT Bio-Pharma successfully identified promising hit compounds.Determined to continue this work beyond my retirement in March 2026, I established CardioGenix to accelerate preclinical development using our proprietary data and technology.Under our mission, "Restoring heart muscle power through science," we are dedicated to providing DCM patients with new therapeutic options.We deeply appreciate your support and collaboration.

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Our DCM model is the TNNT2 gene ΔK210 mutation knock-in mouse established through extensive research at Kyushu University. This model introduces the Troponin T lysine210 deletion mutation, reported in human familial DCM, into the mouse genome, serving as a vital tool for study.

 

This model proves that a decrease in calcium sensitivity is the decisive 'singularity' that triggers the onset of DCM. It accurately reflects human clinical symptoms—including LV dilation and sudden death—requiring careful breeding of heterozygous pairs to produce homozygous subjects for study. While this process is time-intensive, this specific model is the only way to scientifically evaluate pure calcium sensitizers in vivo. It has played a crucial role in our joint development with LTT Bio-Pharma. At CardioGenix, we leverage this proprietary technology to bring innovative treatment alternatives to DCM patients globally.

Proprietary DCM Model Mouse (TNNT2 ΔK210 Knock-in Mouse)

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Join Us as a Partner

Our initiatives are driven by a commitment to support every individual's hope. Join us in opening new horizons for DCM treatment through donations or volunteering.

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