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Clinical Trial Summary

An investigation of the safety and efficacy of tildacerfont in participants with CAH.


Clinical Trial Description

This is a study to evaluate the safety and efficacy of tildacerfont in participants with Congenital Adrenal Hyperplasia (CAH). Treatment will consist of 4 or 12 weeks of continuous dosing followed by safety follow up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05128942
Study type Interventional
Source Spruce Biosciences
Contact Clinical Trials
Phone 415-655-4169
Email CAHptain@sprucebiosciences.com
Status Recruiting
Phase Phase 2
Start date December 10, 2021
Completion date December 2024

See also
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