同辛托品
促肾上腺皮质激素
刺激
考试(生物学)
口译(哲学)
医学
内科学
激素
计算机科学
地质学
古生物学
程序设计语言
作者
Barry R Jones,Junlong Shao,Mitesh Sanghvi,Alejandro Ayala,Rosa Luo,Jian Wang
出处
期刊:Bioanalysis
[Newlands Press Ltd]
日期:2024-06-28
卷期号:: 1-10
标识
DOI:10.1080/17576180.2024.2360358
摘要
Adrenocorticotropic hormone 1-24 (ACTH[1-24]) has a similar effect as endogenous ACTH(1-39) to generate cortisol by targeting the MC2R receptor on the adrenal gland. A new investigational ACTH receptor antagonist drug is being developed to treat diseases of ACTH excess (e.g., Cushing's disease) by binding to the MC2R receptor. Administration of ACTH(1-24) was used in a Phase I clinical study to assess the ability of this drug candidate to suppress the cortisol response to ACTH stimulation. A hybrid immunoaffinity-LCMS assay measuring ACTH(1-24) with a concentration range of 10 to 400 pg/ml was developed to support the study. Consistent and acceptable A&P results were achieved. The assay development and qualification will be discussed.
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