Neurocrine Biosciences' Crinecerfont Shows Results in Pediatric CAH Study

Benzinga · 06/03 11:38

 Neurocrine Biosciences, Inc. (NASDAQ:NBIX) today announced that the primary study results from its CAHtalyst™ Pediatric Phase 3 study investigating crinecerfont for the treatment of congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency have been published in The New England Journal of Medicine online edition and will appear in a future print issue of the journal. The CAHtalyst Pediatric Phase 3 study met the primary and key secondary endpoints related to androgen reduction (during an initial glucocorticoid-stable period) and glucocorticoid (GC) dose reduction while maintaining androgen control. Favorable trends were observed with endpoints that reflect the consequences of long-term supraphysiologic glucocorticoid therapy and androgen excess. In addition to appearing in The New England Journal of Medicine, CAHtalyst Pediatric Phase 3 data were presented at ENDO 2024 (Poster #SUN-441).