To evaluate the safety,tolerability and pharmacokinetics of single intravenous doses of FL058 in healthy Chinese subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
54
Huashan Hospital affiliated to Fudan University
Shanghai, China
Number of patients with adverse events [Safety and Tolerability]
Time frame: Day 1 to Day 7
FL058 -Cmax
To evaluate the PK of single intravenous doses of FL058 in healthy adult human subjects.
Time frame: Up to 48 hours post-dose
FL058 -AUC
To evaluate the PK of single intravenous doses of FL058 in healthy adult human subjects.
Time frame: Up to 48 hours post-dose
FL058 -t1/2
To evaluate the PK of single intravenous doses of FL058 in healthy adult human subjects.
Time frame: Up to 48 hours post-dose
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