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
Latest Information Update: 06 Feb 2025
At a glance
- Drugs Tildacerfont (Primary)
- Indications Congenital adrenal hyperplasia
- Focus Registrational; Therapeutic Use
- Acronyms CAHmelia-204; CAHmelia204
- Sponsors Spruce Biosciences
Most Recent Events
- 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.