drugset / Trial / NCT02830932

Dose-Ranging Trial of Safety & Immunogenicity of an Oral Adenoviral-Vector Based RSV Vaccine (VXA-RSV-f)

NCT02830932 ↗

Phase 1 Completed 66 enrolled Vaxart
RandomizedParallel-groupQuadruple-blindPrevention

Summary

A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Trial to Determine the Safety and Immunogenicity of an Adenoviral-Vector Based Respiratory Syncytial Virus (RSV) F Protein Vaccine (VXA-RSV-f) Expressing Protein F and dsRNA Adjuvant Administered Orally to Healthy Volunteers

Timeline

Start
2016-06-22
Primary completion
2016-09-16
Completion
2017-09-20

Drugs

EvaluationDrugModalityDoseRoute
Subject VXA-RSV-f Vaccine — Oral