HomeTrialNCT07187375
🔬NCT07187375Phase 2RECRUITING

Pharmacokinetics, Safety and Tolerability of Crinecerfont in Participants With Congenital Adrenal Hyperplasia Who Are Less Than 2 Years Old

Study Summary

The main objective for this study is to evaluate the pharmacokinetics (PK) of crinecerfont in pediatric participants 0 to \<2 years of age with congenital adrenal hyperplasia (CAH).

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment6 participants
Primary Completion
Lead SponsorNeurocrine Biosciences
Data Retrieved2026-04-11 04:22:17.614676+00:00
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