hrp0098fc4.4 | Adrenals and HPA Axis 1 | ESPE2024
Sarafoglou Kyriakie
, S. Kim Mimi
, Lodish Maya
, I. Felner Eric
, Martinerie Laetitia
, J. Nokoff Natalie
, Clemente Maria
, Y. Fechner Patricia
, G. Vogiatzi Maria
, W. Speiser Phyllis
, B.G. Rosales Gelliza
, Roberts Eiry
, S. Jeha George
, Farber Robert
, L. Chan Jean
, Ottosson Lars
, Baroncelli Marta
, Dou Zelong
, Nilsson Ola
Introduction: Children with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (CAH) require glucocorticoid (GC) therapy to replace cortisol insufficiency and reduce excess adrenal androgens. Supraphysiological GC doses are typically required, predisposing patients to GC-related comorbidities. In Phase 2 studies, participants with CAH who received crinecerfont, a novel oral CRF1 antagonist, experienced reduction of the adrenal a...