drugset / Trial / NCT01761123

Immunogenicity of Seasonal Influenza by Delivery Directly to Ileum

NCT01761123

Phase 1 Completed 37 enrolled Vaxart
NaSingle-groupOpen-labelPrevention

Summary

the purpose of the study is to determine the safety and tolerability of VXA-A1.1, an adjuvanted adenoviral based influenza vaccine, when delivery is targeted to the ileum, using a radio controlled capsule. The secondary objective is to evaluate the immune response (cellular and humoral) of two doses of VXA-A1.1 oral vaccine.

Timeline

Start
2013-01
Primary completion
2014-10
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject VXA-A1.1 Vaccine Oral

Indications