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).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
7
Oral solution
Neurocrine Clinical Site
Berlin, Germany
Neurocrine Clinical Site
Düsseldorf, Germany
Neurocrine Clinical Site
Heidelberg, Germany
Plasma Concentration of Crinecerfont
Time frame: Days 7 and 15
Number of Participants With Treatment-emergent Adverse Events (TEAEs)
Time frame: Up to Month 37
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