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Study identifier: NCT07144163 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study to Evaluate Atumelnant in Adults With Congenital Adrenal Hyperplasia

Condition: Congenital Adrenal Hyperplasia · Classic Congenital Adrenal Hyperplasia  ·  Sponsor: Crinetics Pharmaceuticals Inc.

PhasePhase 3
Planned participants150
Who can joinAll sexes, 18 Years to 74 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Crinetics Clinical Trials  ·  833-827-9741  ·  clinicaltrials@crinetics.com

Always discuss trial participation with your own doctor first.

Locations (55)

Crinetics Study SiteLos Angeles, California, United StatesRecruiting
Crinetics Study SiteAtlanta, Georgia, United StatesRecruiting
Crinetics Study SiteChicago, Illinois, United StatesRecruiting
Crinetics Study SiteBaltimore, Maryland, United StatesRecruiting
Crinetics Study SiteAnn Arbor, Michigan, United StatesRecruiting
Crinetics Study SiteMinneapolis, Minnesota, United StatesRecruiting
Crinetics Study SiteRochester, Minnesota, United StatesRecruiting
Crinetics Study SitePittsburgh, Pennsylvania, United StatesRecruiting
Crinetics Study SiteDallas, Texas, United StatesRecruiting
Crinetics Study SiteMilwaukee, Wisconsin, United StatesRecruiting
Crinetics Study SiteBuenos Aires, Buenos Aires F.D., ArgentinaRecruiting
Crinetics Study SiteBuenos Aires, Buenos Aires F.D., ArgentinaRecruiting

+ 43 more locations — full list on the registry record.

Follow this study

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Source record: clinicaltrials.gov/study/NCT07144163