The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of PF-06946860 in healthy adult Japanese participants following single dose administration.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Enrollment
8
PF-06946860 administered subcutaneously
Placebo administered subcutaneously
Anaheim Clinical Trials LLC-Clinical Research
Anaheim, California, United States
Incidence of participants experiencing AE
Time frame: Up to 20 weeks post-dose
Maximum Observed PF-06946860 Concentration (Cmax)
Time frame: Up to 20 weeks post-dose
Area Under the Curve From Time Zero to Last Quantifiable PF-06946860 Concentration (AUClast)
Time frame: Up to 20 weeks post-dose
Time to Reach Maximum Observed PF-06946860 Concentration (Tmax)
Time frame: Up to 20 weeks post-dose
PF-06946860 Half-Life (t1/2)
Time measured for the PF-06946860 concentration to decrease by one half.
Time frame: Up to 20 weeks post-dose, as data permit
Incidence of development of ADA, and if necessary NAb, against PF-06946860
Time frame: Up to 20 weeks post-dose, as data permit
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