Treatment of muscle disease characterized by insulin resistance
AssigneesFate Therapeutics, (Canada) Inc., Ottaw Hospital Research Institute
InventorsLynn Megeney, Carol Evans
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AssigneesFate Therapeutics, (Canada) Inc., Ottaw Hospital Research Institute
InventorsLynn Megeney, Carol Evans
Estimating the term…
It is reported herein that certain muscle diseases and conditions, including forms of muscular dystrophy, are characterized by impaired insulin-dependent signaling in the muscle tissue, in essence, a form of insulin resistance. The present disclosure relates to therapeutic agents, compositions and methods for treating a muscle disease or condition characterized by impaired insulin-dependent signaling by targeting components of the defective insulin signaling pathway. The disease or condition may be treated by administering a therapeutic agent that activates the insulin signaling pathway, in particular, therapeutic agents that act post-insulin receptor to modulate intracellular effector molecules. An exemplary modulator is metformin. Metformin may be administered alone or may be coadministered with another therapeutic agent for treating the muscle disease or condition, such as a corticosteroid.
A method of treating a muscle disease or condition comprising administering to a subject in need thereof a therapeutically effective amount of a therapeutic agent that is metformin or an analog or derivative thereof, wherein the muscle disease or condition is Duchenne muscular dystrophy.
A method of treating a muscle disease characterized by impaired insulin-dependent signaling comprising administering to a patient a therapeutically effective amount of metformin, wherein the muscle disease is Duchenne muscular dystrophy.
Dependencies are inferred from the claim text.