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
Number of Participants With Treatment-emergent Adverse Events (TEAE)
Time frame: Day 1 up to 28 weeks
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