Phase 1, open-label, parallel, active-controlled, multiple IV dose, proof of concept study conducted at one study center in the United States (US).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Enrollment
54
Celerion
Lincoln, Nebraska, United States
Measurement of subsets of WBC
Time frame: 10 days
Number of adverse events as a measure of safety and tolerability
Time frame: 19 days
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