drugset / Trial / NCT07536269

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Crinecerfont in Participants With Classic Congenital Adrenal Hyperplasia (CAH) Who Are Less Than 4 Years Old

NCT07536269

Phase 2 Not yet recruiting 20 enrolled Neurocrine Biosciences
NaSingle-groupOpen-labelTreatment

Summary

The main objective of this study is to assess the safety and tolerability of crinecerfont in pediatric participants 3 months to \<4 years of age with CAH.

Timeline

Start
2026-04
Primary completion
2028-03
Completion
2028-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Crinecerfont Small molecule Oral