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Tildacerfont for the Treatment of Patients With Classic Congenital Adrenal Hyperplasia: Results From a 12-Week Phase 2 Clinical Trial in Adults With Classic CAH

Background: Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21-OHD) is an autosomal recessive disorder characterized by insufficient cortisol production resulting in excess adrenocorticotropic hormone (ACTH) and adrenal androgen production. Standard-of-care therapy with glucoc...

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Detalles Bibliográficos
Autores principales:	Auchus, Richard Joseph, Merke, Deborah P, Madu, Ivy-Joan, Nakhle, Samer, Sarafoglou, Kyriakie, Huang, Michael, Moriarty, David, Barnes, Chris, Newfield, Ron S
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2021
Materias:	Endocrine Disruption
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8090554/ http://dx.doi.org/10.1210/jendso/bvab048.1011

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