- An Extension Study to Evaluate Safety and Efficacy of Atumelnant in Participants With Congenital Adrenal Hyperplasia — Recruiting • Phase II • NCT06712823.
- Long-term study testing whether atumelnant is safe and effective for treating congenital adrenal hyperplasia.
Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
The purpose of this study is to evaluate the long-term safety, tolerability, and efficacy of atumelnant (CRN04894). Conditions: Congenital Adrenal Hyperplasia, Classic Congenital Adrenal Hyperplasia Interventions: atumelnant (CRN04894) Lead Sponsor: Crinetics Pharmaceuticals Inc. Planned Enrollment: 200 participants