Double blinded, randomized, placebo-controlled, dose finding, multi-center, phase 1 trial in 48 healthy volunteer subjects. After completion of screening procedures, the subjects are randomized to one of four treatment groups (different dosage strengths and placebo) All subjects will receive study treatment at day 0 and will return on day 28. Subjects randomized to treatment groups with two vaccinations will receive a second treatment at day 28. Subjects will return on day 56 for the final visit.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
48
Medical University of Vienna, Center for Pathophysiology, Infectiology and Immunology
Vienna, Austria
Medical University of Vienna, Department of Clinical Pharmacology
Vienna, Austria
Immunogenicity: Functional anti-Zika antibodies as measured by PRNT
Functional anti-Zika antibodies as measured by PRNT.
Time frame: 56 days
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