This is a single-center evaluation of Aldafermin (NGM282) in an open-label, single-dose and parallel group study in participants with Impaired Renal Function.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
48
Single 3 mg dose
NGM Clinical Study Site
Miami, Florida, United States
Maximum observed plasma concentration (Cmax) of aldafermin (Day 1 through Day 4)
Time frame: 12 Days
Area under the concentration-time curve from time zero extrapolated to infinity (AUC 0-infinity) of aldafermin (Day 1 through Day 4)
Time frame: 12 Days
Type and frequency of Adverse Events (Day 1 through Day 11)
Time frame: 12 Days
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