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Evaluate the Safety, Efficacy, and Pharmacokinetics of CRN04894 in Participants With Congenital Adrenal Hyperplasia (TouCAHn)

Congenital Adrenal Hyperplasia Clinical Trial

Official title:
A 12-week, Phase 2 Open-label, Sequential Dose Cohort Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of CRN04894 Treatment in Participants With Congenital Adrenal Hyperplasia (TouCAHn)

Clinical Trial Summary

The purpose of this Phase 2, open-label, sequential dose cohort study is to evaluate the safety, efficacy, and pharmacokinetics (PK) of CRN04894 in participants with classic congenital adrenal hyperplasia (CAH) caused by 21-hydroxylase deficiency.

Clinical Trial Description

This Phase 2, open-label, sequential dose cohort study will evaluate the efficacy, safety, PK, and PD of CRN04894 when administered for 12 weeks in participants with CAH caused by 21-hydroxylase deficiency. Up to approximately 30 participants will be enrolled in the study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05907291
Study type Interventional
Source Crinetics Pharmaceuticals Inc.
Contact Crinetics Clinical Trials
Phone 833-827-9741
Email clinicaltrials@crinetics.com
Status Recruiting
Phase Phase 2
Start date July 3, 2023
Completion date March 2025
View Details
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