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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Oral solution
Neurocrine Clinical Site
San Francisco, California, United States
RECRUITINGNeurocrine Clinical Site
Aurora, Colorado, United States
RECRUITINGNumber of Participants With Treatment-emergent Adverse Events (TEAE)
Time frame: Day 1 up to 28 weeks
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Neurocrine Clinical Site
Hartford, Connecticut, United States
RECRUITINGNeurocrine Clinical Site
Atlanta, Georgia, United States
RECRUITINGNeurocrine Clinical Site
Chicago, Illinois, United States
RECRUITINGNeurocrine Clinical Site
Indianapolis, Indiana, United States
RECRUITINGNeurocrine Clinical Site
Ann Arbor, Michigan, United States
RECRUITINGNeurocrine Clinical Site
Minneapolis, Minnesota, United States
RECRUITINGNeurocrine Clinical Site
Philadelphia, Pennsylvania, United States
RECRUITINGNeurocrine Clinical Site
Dallas, Texas, United States
RECRUITING...and 1 more locations