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Type 1 diabetes affects approximately one million Americans, and is usually diagnosed in children
and young adults. Type 1 diabetes arises from the autoimmune destruction of islet cells in the
pancreas. Due to the body's inability to produce insulin, insulin must be replaced, primarily
through daily injections, in order to control plasma glucose.
While insulin replacement provides a life-sustaining therapy, it is not a cure, and many individuals
develop significant disease-associated complications, including those of the eye, kidney, and heart.
While progress has been made in the ability to identify individuals likely to develop the disorder,
scientific understanding of the disease has been limited by practical considerations in studying
humans with the condition.
Much of the understanding of the disease is derived from rodent models, particularly the non-obese
diabetic (NOD) mouse. Although numerous therapies have been shown to inhibit the development of type
1 diabetes in this model, the success in advancing therapies to human patients has been limited.
In collaboration with the American Diabetes Association, Entelos developed the Type 1 Diabetes
PhysioLab platform to address key scientific questions related to the disease's onset and
progression in the NOD mouse. This platform is currently being used to develop a better
understanding of the human disease, and research within it has already yielded insights into how
discrepancies in dosing, duration, and timing could potentially account for the failure of many
clinically tested type 1 diabetes therapies.
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