U.S., Aug. 28 -- ClinicalTrials.gov registry received information related to the study (NCT07144163) titled 'A Study to Evaluate Atumelnant in Adults With Congenital Adrenal Hyperplasia' on Aug. 20.
Brief Summary: The purpose of this study is to evaluate the efficacy, safety, PK, and PD of atumelnant in adults with classic CAH due to 21-OHD.
Study Start Date: Sept., 2025
Study Type: INTERVENTIONAL
Condition:
Congenital Adrenal Hyperplasia
Classic Congenital Adrenal Hyperplasia
Intervention:
DRUG: Atumelnant
Atumelnant, tablets, once daily by mouth
DRUG: Placebo
Placebo, tablets, once daily by mouth
Recruitment Status: NOT_YET_RECRUITING
Sponsor: Crinetics Pharmaceuticals Inc.
Disclaimer: Curated by HT Syndication....