We are addressing a critical unmet need for people with inherited sarcomere variants.

Image Genetic Dilated Cardiomyopathy
Dilated cardiomyopathy (DCM) is a cardiac muscle disorder affecting the heart’s main ventricular and atrial chambers, making it difficult to pump blood to the rest of the body. Nearly 40% of DCM is caused by underlying genetic variants. With more than 70 genes implicated in DCM, the most common variant is in genes of the sarcomere, the heart’s contractile machinery, including the TTN and MYH7 genes being among the most common.

Genetic DCM carries significant risk of disease progression to advanced stages of heart failure. Occurring in as many as one in every 250 people, DCM is the leading cause of heart transplants globally. Despite the availability of treatments to address symptoms, there are no therapies that specifically target the underlying causes of primary DCM. An important opportunity exists to create a new standard of care for this progressive disease and restore cardiac function by targeting sarcomeric gene variants to prevent disease progression.

Danicamtiv and Genetic Dilated Cardiomyopathy

Danicamtiv is an investigational direct myosin activator that is designed to selectively restore myosin motor function. In patients with DCM caused by sarcomeric gene variants, danicamtiv aims to improve cardiac function, potentially slowing the progression of heart failure.

Kardigan is advancing danicamtiv, a potential first-in-class direct myosin activator targeting genetic DCM driven by sarcomeric variants, to restore cardiac function through direct activation of both atrial and ventricular function. Data presented at the Heart Failure Society of America’s Annual Scientific Meeting 2025 and published in the Journal of the American College of Cardiology (JACC) demonstrated that in a Phase 2 study, danicamtiv treatment was associated with statistically significant improvements in left atrial function index and left ventricular ejection fraction, particularly in patients with genetic DCM driven by sarcomeric variants.

These data support the hypothesis that danicamtiv directly activates myosin and corrects the dysfunction resulting from sarcomeric variants in people with DCM and provides a strong rationale for further investigation. The KINSHIP-DCM Phase 2b/3 clinical trial is currently recruiting participants to evaluate the safety and efficacy of danicamtiv as a potential first-in-class treatment for genetic DCM. Learn more about KINSHIP-DCM here.

Kardigan in-licensed exclusive worldwide development and commercialization rights to danicamtiv, an investigational drug discovered at MyoKardia and further developed by Bristol Myers Squibb.