This randomized, double-blind, placebo-controlled, parallel-group study will evaluate the safety and pharmacokinetics of subcutaneous lebrikizumab in healthy Japanese volunteers. Healthy Japanese and Caucasian volunteers will be randomized to receive a single subcutaneous dose of either lebrikizumab or placebo.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
60
Dose-level cohorts receiving single subcutaneous dose
single dose subcutaneously
Unnamed facility
Honolulu, Hawaii, United States
Safety: Incidence of adverse events in healthy Japanese subjects
Time frame: 120 days
Pharmacokinetics in healthy Japanese subjects: Area under the concentration-time curve (AUC)
Time frame: 120 days
Comparison of safety (incidence of adverse events) in healthy Japanese and Caucasian subjects
Time frame: approximately 5 months
Comparison of pharmacokinetics (AUC) in healthy Japanese and Caucasian subjects
Time frame: approximately 5 months
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