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Clinical Trial ● Currently Recruiting Phase II NCT06712823

An Extension Study to Evaluate Safety and Efficacy of Atumelnant in Participants With Congenital Adrenal Hyperplasia

An Extension Study to Evaluate Safety and Efficacy of Atumelnant in Participants With Congenital Adrenal Hyperplasia — Recruiting • Phase II • NCT06712823.

📅 29 Jun 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase II
NCT ID
NCT06712823
Start
2025-02-25
Completion
2029-07
ClinicaliQ Trial Snapshot
  • 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.

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  • Quick orientation before opening the registry record.
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What This Trial Is Studying

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

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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