Neurocrine biosciences announces u.s. fda accepts new drug applications and grants priority review for crinecerfont for pediatric and adult patients with cah

Pdufa target action dates in late december 2024 highly selective crf1 antagonist is the potential first new treatment for cah in 70 years san diego , july 1, 2024 /prnewswire/ -- neurocrine biosciences, inc. (nasdaq: nbix) today announced the u.s. food and drug administration (fda) has accepted its two new drug applications (nda) with priority review designations for crinecerfont in the treatment of children, adolescents and adults with classic congenital adrenal hyperplasia (cah). if approved, crinecerfont would be the first new treatment option for cah in 70 years and a first-in-class therapy, with a novel approach for the treatment of this rare and serious endocrine disorder.
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