Study of NGM395 in adult participants.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
38
NGM Clinical Study Site
Brisbane, Australia
Incidence and Severity of Treatment-Emergent Adverse Events (TEAEs)
The number and percent of patients reporting treatment emergent adverse events (TEAEs) by cohort.
Time frame: 140 Days
Serum Concentration of NGM395
NGM395 concentration data by cohort
Time frame: 140 Days
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NGM395 Dose 4
NGM395 Dose 5
NGM395 Dose 6
Placebo