The purpose of this study is to evaluate the safety and tolerability of single doses of ILV-095 in healthy Japanese male subjects.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
48
Pfizer Investigational Site
Tokyo, Japan
Safety and tolerability will be evaluated from the reported AEs including any injection-site reactions, physical examinations, vital sign measurements, cardiac rhythm monitoring, 12-lead ECGs, and clinical laboratory test results.
Time frame: 3 weeks per group
Pharmacokinetic parameters
Time frame: 3 weeks per group
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.