The primary objective of the study is to evaluate the safety and tolerability of 3 single ascending subcutaneous (SC) doses and 1 single intravenous (IV) dose of REGN6490 in healthy first-generation Japanese adult participants The secondary objectives of the study are: * To characterize the pharmacokinetic (PK) profile of single SC and IV doses of REGN6490 in healthy first-generation Japanese adult participants * Assess immunogenicity of REGN6490 in healthy first-generation Japanese adult participants dosed with a single IV or SC dose of REGN6490
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
19
Single dose of REGN6490
Placebo matching single dose of REGN6490
Regeneron Study Site
Glendale, California, United States
Incidence and severity of Treatment-Emergent Adverse Events (TEAEs)
TEAEs include abnormal laboratory testing, vital signs and electrocardiograms (ECGs)
Time frame: Up to Week 16
Serum Concentration of REGN6490 over time
Time frame: Up to Week 16
Incidence of Treatment-Emergent REGN6490 Anti-Drug Antibodies (ADAs)
Time frame: Up to Week 16
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