The purpose of this study is to evaluate safety and tolerability after administration of KHK4951 in healthy volunteers and patients with wet age-related macular degeneration.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
116
Hakata clinic
Fukuoka, Japan
Number of participants with adverse events
For adverse events that occurred after administration of the investigational drug, number of subjects with AEs and occurrence frequency are evaluated.
Time frame: Day 1 to Day 43
Serum KHK4951 concentration
Time frame: Healthy Volunteers: Day 1, Day2, Day4, Day8, Day12, Day16, Day21, Day23, Day 25, Day 29, Day 36, Day 43; Patients: Day 1, 8, 22, 43
Time to the maximum concentration
Time frame: Day 1 to Day 43
The maximum concentration
Time frame: Day 1 to Day 43
Area under the concentration-time curve
Time frame: Day 1 to Day 43
Apparent clearance
Time frame: Day 1 to Day 43
Elimination half-life
Time frame: Day 1 to Day 43
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