Clin2
NCT06712823Possibly a fitRecruiting

Long-term safety study of atumelnant for adrenal hyperplasia

Congenital Adrenal HyperplasiaClassic Congenital Adrenal Hyperplasia

Treatments studied

Part of Genetic & congenital, Hormones & metabolism, Kidney & urinary, Women’s health & pregnancy clinical trials.

This study tests the long-term safety and effectiveness of the study drug atumelnant for people with congenital adrenal hyperplasia. It is for those who have already completed a previous atumelnant study and may benefit from continuing treatment.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 2
Enrollment
200 people
Ages
16 years to 74 years
Study type
Interventional

Who can take part

  • You must have finished a previous Crinetics study of atumelnant for congenital adrenal hyperplasia.
  • Women who could get pregnant must agree to use highly effective birth control during the study and for 2 weeks after the last dose.
  • If you are a man, you must use a condom with a partner who could become pregnant, or be abstinent, during the study and for 2 weeks after the last dose.
  • You cannot have serious medical conditions like heart disease, severe kidney or liver problems, uncontrolled diabetes, or a history of alcohol or drug abuse in the past year.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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