This is a Phase I/IIa randomized, double-blind, placebo-controlled study to evaluate the safety, reactogenicity, and immunogenicity of 3 potencies (dosages) of H5N1 VLP vaccine or placebo in healthy adults 18 to 40 years of age.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
230
Two doses - Day 0 \& Day 28
Two doses - Day 0 \& Day 28
Healthcare Discoveries, Inc.
San Antonio, Texas, United States
Safety and reactogenicity of H5N1 VLP Vaccine
Time frame: 6 months
Immunogenicity of H5N1 VLP Influenza vaccine
Time frame: 6 months
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