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

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NCT06712823 · readout ≤ 1,077 d

Sponsored by Crinetics Pharmaceuticals Inc. (industry) · CRNX — their whole pipeline →.

Phase
Phase 2
Status
Recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
200estimated
Sites
13
Countries
Argentina, Brazil, Germany +3

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-02-25actualWhen the study began enrolling
Primary completionJul 2029estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionAug 2029estimatedThe whole study's end, after follow-up
First posted2024-12-02actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Congenital Adrenal Hyperplasia
  • Classic Congenital Adrenal Hyperplasia

Intervention

  • Drug: atumelnant (CRN04894)

Primary outcomes

what the primary-completion date above is the date OF
Incidence of treatment-emergent adverse events (TEAEs), including treatment-emergent serious adverse events (SAEs), adverse events of special interest (AESI [adrenal insufficiency]) and any adverse events (AEs) leading to discontinuation
measured Week 108
Incidence of glucocorticoid (GC) deficiency / adrenal insufficiency and adrenal crisis
measured Week 108
Incidence of hospitalizations related to congenital adrenal hyperplasia (CAH)
measured Week 108
Change from baseline in morning (before 11:00 AM) serum androstenedione (A4) over time
measured Week 108

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