The objective of this study is to compare the pharmacokinetic and pharmacodynamic properties and safety profile of alefacept in Caucasian and Japanese healthy subjects
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
QUADRUPLE
Enrollment
75
Unnamed facility
Glendale, California, United States
Serum alefacept pharmacokinetic parameters
Time frame: Days 1-8,15, 22, 29 and 43
Pharmacodynamic parameters of total lymphocyte count and peripheral lymphocyte subsets
Time frame: Days 1-8, 15, 22, 29 and 43
Safety variables including anti-alefacept antibodies
Time frame: Days 1-8, 15, 22, 29 and 43
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