In the USA, two New Drug Applications (NDA) for crinecerfont have been accepted by the US regulator, and will be considered under the Priority Review scheme.
Developed by Neurocrine Biosciences (Nasdaq: NBIX), crinecerfont is intended for the treatment of classic congenital adrenal hyperplasia (CAH), a genetic disorder that affects the adrenal glands.
If approved, crinecerfont would be the first new treatment for CAH in 70 years, offering a novel approach to this rare endocrine disorder.
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