A PHASE 1, RANDOMIZED, RATER AND SUBJECT BLINDED PLACEBO CONTROLLED STUDY TO EVALUATE THE SAFETY, REACTOGENICITY, TOLERABILITY AND IMMUNOGENICITY OF A STANDARD AND A FRACTIONAL DOSE OF H1 INFLUENZA VACCINE DELIVERED BY VX-103 (A MIMIX MICRONEEDLE PATCH (MAP) SYSTEM) IN HEALTHY ADULTS ¿18-39 YEARS OF AGE.
- Registry ID
- VAX-103-01
- Source registry
- HEALTH_CANADA
- Status
- Ongoing
- Phase
- PHASE1
- Study type
- INTERVENTIONAL
- Sponsor
- VAXESS TECHNOLOGIES
- Start date
- 2022-07-14
- Last update
- 2022-06-23
Conditions
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