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A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SPR001 (Tildacerfont) in Reducing Supraphysiologic Glucocorticoid Use in Adult Subjects With Classic Congenital Adrenal Hyperplasia

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Trial Profile

A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of SPR001 (Tildacerfont) in Reducing Supraphysiologic Glucocorticoid Use in Adult Subjects With Classic Congenital Adrenal Hyperplasia

Status: Active, no longer recruiting
Phase of Trial: Phase II

Latest Information Update: 29 Jul 2024

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At a glance

  • Drugs Tildacerfont (Primary)
  • Indications Congenital adrenal hyperplasia
  • Focus Registrational; Therapeutic Use
  • Acronyms CAHmelia-204; CAHmelia204
  • Sponsors Spruce Biosciences

    • Most Recent Events

    • 13 May 2024 According to a Spruce Biosciences media release, End of Phase 2 (EOP2) meeting with the U.S. Food and Drug Administration (FDA) planned in the first quarter of 2025.
    • 13 May 2024 According to a Spruce Biosciences media release,Poster Highlighting Baseline Characteristics Presented at the PES 2024 Annual Meeting.
    • 22 Apr 2024 According to a Spruce Biosciences media release, Paul Thornton is principal Investigator of this study.

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