Assessment of Steroid Hormones in Both Saliva and Blood During a Phase 2 Clinical Trial for the Use of Tildacerfont in Adults With Classic Congenital Adrenal Hyperplasia

Background: Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency is an autosomal recessive disorder characterized by an inability to synthesize endogenous cortisol resulting in overproduction of 17-hydroxyprogesterone (17-OHP) and androgens such as androstenedione (A4). Serum-based...

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Detalles Bibliográficos
Autores principales: Keevil, Brian, Sarafoglou, Kyriakie, Moriarty, David, Huang, Michael, Barnes, Chris, Arlt, Wiebke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Tumor Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8089208/
http://dx.doi.org/10.1210/jendso/bvab048.2070

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8089208/
http://dx.doi.org/10.1210/jendso/bvab048.2070

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