This study is an open-label, multicenter evaluation of Safety and Pharmacokinetics of N1539 in postoperative Pediatric subjects aged 2 to \<17 years.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
19
Once daily
Research Center
Sheffield, Alabama, United States
Research Center
Bakersfield, California, United States
Research Center
Salt Lake City, Utah, United States
Number of Subjects Experiencing an AE
Number of study subjects who experienced an AE
Time frame: Through study completion, approximately 28 Days
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