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A Phase 2, Open-Label, Multiple-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of NBI-74788 in Pediatric Subjects With Congenital Adrenal Hyperplasia

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Trial Profile

A Phase 2, Open-Label, Multiple-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of NBI-74788 in Pediatric Subjects With Congenital Adrenal Hyperplasia

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 24 Jul 2024

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At a glance

  • Drugs Crinecerfont (Primary)
  • Indications Congenital adrenal hyperplasia
  • Focus Adverse reactions
  • Sponsors Neurocrine Biosciences

    • Most Recent Events

    • 21 Sep 2023 According to a Neurocrine Biosciences media release, results of post-hoc analysis will be presented at the 61st Annual European Society for Pediatric Endocrinology (ESPE) Meeting 2023.
    • 21 Sep 2023 Results of post-hoc analysis presented in the Neurocrine Biosciences Media Release.
    • 22 May 2023 Results assessing the safety, tolerability, and efficacy of crinecerfont in adolescents with 21-hydroxylase deficiency Congenital Adrenal Hyperplasia published in the Journal of Clinical Endocrinology and Metabolism

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