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