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Neurocrine Biosciences Presents New Two-Year CRENESSITY® (crinecerfont) Data Demonstrating Durable Hormone Control, Reduced Glucocorticoid Exposure and Meaningful Clinical Improvements in Pediatric Patients with Classic Congenital Adrenal Hyperplasia

Neurocrine Biosciences, Inc. (Nasdaq: NBIX) today announced the presentation of new two-year data from the Phase 3 CAHtalyst® Pediatric study demonstrating durable androgen control, sustained decreases in glucocorticoid (GC) doses and meaningful improvements in clinical outcomes associated with excess androgens and long-term GC exposure in children and adolescents with classic congenital adrenal hyperplasia treated with CRENESSITY® (crinecerfont).

articleNeurocrine Biosciences, Inc.May 1, 202613/company/neurocrine-biosciences-inc/news/neurocrine-biosciences-presents-new-two-year-crenessityr-crinecerfont-data-demonstrating-durable-hormone-control-reduced-glucocorticoid-exposure-and-meaningful-clinical-improvements-in-pediatric-patients-with-classic-congenital-adrenal-hyperplasia
Neurocrine Biosciences Presents New Two-Year CRENESSITY® (crinecerfont) Data Demonstrating Durable Hormone Control, Reduced Glucocorticoid Exposure and Meaningful Clinical Improvements in Pediatric Patients with Classic Congenital Adrenal Hyperplasia

About this update from Neurocrine Biosciences, Inc.

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More updates from Neurocrine Biosciences, Inc.

congenital adrenal hyperplasiaNeurocrine Biosciencesinsulin resistanceGCCRENESSITYbody mass indexadrenocorticotropic hormoneglucocorticoidmeaningful improvementsclinical outcomes