The purpose of this study is to evaluate the efficacy, safety, and pharmacokinetics of beloranib in obese subjects with hypothalamic injury.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
14
ZGN-440 sterile diluent/placebo
Children's Hospitals and Clinics of Minnesota
Saint Paul, Minnesota, United States
Vanderbilt University Medical Center
Nashville, Tennessee, United States
The Boden Institute
Sydney, New South Wales, Australia
Austin Health, Metabolic Disorders Centre
Heidelberg Heights, Victoria, Australia
Change in body weight from baseline to the end of the randomized dosing period.
Time frame: 4 weeks
Change in lipid profile (cholesterol, LDL, HDL, triglycerides) from baseline to the end of the randomized dosing period
Time frame: 4 weeks
Change in hs-CRP from baseline to the end of the randomized dosing period.
Time frame: 4 weeks
Change in hunger from baseline to the end of the randomized dosing period.
Time frame: 4 weeks
Change in quality of life from baseline to the end of the randomized dosing period.
Time frame: 4 weeks
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