Lundbeck’s Asedebart Receives the US FDA Orphan Drug Designation for Endogenous Cushing’s Syndrome

Shots:

• The US FDA has granted Orphan Drug Designation (ODD) to asedebart (Lu AG13909) for the treatment of endogenous Cushing’s syndrome
• Lundbeck is evaluating efficacy and safety of asedebart in proof-of-concept trials for Cushing’s disease & classic congenital adrenal hyperplasia (CAH) 
• Asedebart is a humanized anti-ACTH monoclonal antibody that blocks ACTH signaling at the adrenal glands, reducing the secretion of glucocorticoids, mineralocorticoids & androgens

Ref: PRnewswire  |  Image: Lundbeck  |  Press Release

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