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Vaccine
Vaccine Dose Group 8 mcg dose for Influenza
Phase 2
Waitlist Available
Research Sponsored by VaxInnate Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through day 90
Awards & highlights
Study Summary
This is a multi-center, randomized, double-blind, active comparator controlled study in which up to 450 healthy adults age 18-64 years will be administered either one of two dose levels of VAX2012Q or a licensed quadrivalent influenza vaccine. The subjects will be randomized at a 1:1:1 ratio.
Eligible Conditions
- Influenza
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through day 90
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through day 90
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Seroconversion rates to the 4 components of VAX2012Q
Secondary outcome measures
C-reactive protein levels
Immunogenicity of the two dose levels of VAX2012Q and of Fluzone Quadrivalent
Long term safety following vaccination assessed by Clinically significant AEs
+1 moreOther outcome measures
Breadth of immunity
Duration of immunity
Trial Design
3Treatment groups
Experimental Treatment
Active Control
Group I: Vaccine Dose Group 8 mcg doseExperimental Treatment1 Intervention
VAX2012Q, 8 mcg dose
Group II: Vaccine Dose Group 12 mcg doseExperimental Treatment1 Intervention
VAX2012Q, 12 mcg dose
Group III: ControlActive Control1 Intervention
Fluzone Quadrivalent vaccine
Find a Location
Who is running the clinical trial?
AccelovanceIndustry Sponsor
15 Previous Clinical Trials
3,593 Total Patients Enrolled
VaxInnate CorporationLead Sponsor
11 Previous Clinical Trials
1,704 Total Patients Enrolled
Department of Health and Human ServicesFED
226 Previous Clinical Trials
928,499 Total Patients Enrolled
Frequently Asked Questions
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