The objective of this clinical study is to evaluate the efficacy and safety of NTRA-9620 compared with placebo in pediatric subjects (aged 28 weeks postmenstrual age to 52 weeks old) with SBS following surgical resection
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
2
Lucile Packard Children's Hospital Stanford
Palo Alto, California, United States
Connecticut Children's Hospital
Hartford, Connecticut, United States
University of Florida
Gainesville, Florida, United States
Children's Mercy Hospital
Kansas City, Missouri, United States
Percent Change in %PN/IV
Percent change in %PN/IV from baseline based on caloric intake
Time frame: baseline and end of treatment or 24 weeks, whichever occurs first
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Cincinnati Children's Hospital
Cincinnati, Ohio, United States
Nationwide Children's Hospital
Columbus, Ohio, United States
Texas Children's Hospital
Houston, Texas, United States
Seattle Children's Hospital
Seattle, Washington, United States