drugset / Trial / NCT04199169

Safety and Immunogenicity of a Nipah Virus Vaccine

NCT04199169 ↗

RandomizedParallel-groupTriple-blindPrevention

Summary

A first-in-human, phase 1 trial is to be conducted in a healthy adult population in the US to assess the safety and immunogenicity of three ascending Nipah vaccine (HeV-sG-V; Hendra virus soluble glycoprotein vaccine) dosages. Different dosing regimens and number of doses will also be explored.

Timeline

Start
2020-02-18
Primary completion
2022-05-06
Completion
2022-05-06

Drugs

EvaluationDrugModalityDoseRoute
Subject HeV-sG-V Vaccine 10 ug —
Subject HeV-sG-V Vaccine 30 ug —
Subject HeV-sG-V Vaccine 100 ug —

Indications