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A Phase 2/3 Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Atumelnant Treatment in Pediatric Participants With Congenital Adrenal Hyperplasia Including a Long-Term Extension

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Trial Profile

A Phase 2/3 Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Atumelnant Treatment in Pediatric Participants With Congenital Adrenal Hyperplasia Including a Long-Term Extension

Status: Recruiting
Phase of Trial: Phase II/III

Latest Information Update: 11 Dec 2025

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At a glance

  • Drugs Atumelnant (Primary)
  • Indications Congenital adrenal hyperplasia
  • Focus Registrational; Therapeutic Use
  • Acronyms Balance-CAH
  • Sponsors Crinetics Pharmaceuticals

Most Recent Events

  • 28 Nov 2025 Planned initiation date changed (estimated date of first patient enrollment) from 1 Sep 2025 to 30 Nov 2025.
  • 28 Nov 2025 Status changed from not yet recruiting to recruiting.
  • 06 Nov 2025 According to a Crinetics Pharmaceuticals media release, company expects the first patients to randomize in this trial in the fourth quarter of 2025.

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