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A 3-Month Phase 2 Study to Evaluate the Safety and Efficacy of SPR001 in Subjects With Classic Congenital Adrenal Hyperplasia

Trial Profile

A 3-Month Phase 2 Study to Evaluate the Safety and Efficacy of SPR001 in Subjects With Classic Congenital Adrenal Hyperplasia

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

Latest Information Update: 19 Sep 2019

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At a glance

  • Drugs Tildacerfont (Primary)
  • Indications Congenital adrenal hyperplasia
  • Focus Adverse reactions
  • Sponsors Spruce Biosciences
  • Most Recent Events

    • 19 Sep 2019 According to a Spruce Biosciences media release, Richard Auchus (M.D., Ph.D.) is an investigator in this study and professor of internal medicine and pharmacology, division of metabolism, endocrinology and diabetes at University of Michigan, Ann Arbor.
    • 19 Sep 2019 According to a Spruce Biosciences media release, full results of the study will be reported at an upcoming medical conference.
    • 19 Sep 2019 Results presented in a Spruce Biosciences media release.
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