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A Phase 2 Study to Evaluate the Safety, Efficacy and PK of Tildacerfont in Children With CAH

Congenital Adrenal Hyperplasia Clinical Trial

Official title:
A Phase 2 Study to Evaluate the Safety, Efficacy and Pharmacokinetics of SPR001 (Tildacerfont) in Children Aged 2 to 17 Years With Congenital Adrenal Hyperplasia

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

Clinical Trial Details
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
View Details
See also
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