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 Hyperpla

Status: Discontinued

Phase of Trial: Phase II

Latest Information Update: 13 Oct 2025

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At a glance

03 Feb 2025 According to ClinicalTrials.gov record, this trial was Terminated as Study did not meet its primary endpoint
03 Feb 2025 Status changed from active, no longer recruiting to discontinued.
06 Jan 2025 Planned End Date changed from 1 Sep 2029 to 31 Jan 2025.

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