drugset / Trial / NCT01188512

First Adult Safety Trial on Nasal Live Attenuated B. Pertussis Vaccine

NCT01188512

RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to evaluate the safety and immunogenicity of a new live attenuated vaccine against whooping-cough. It is a phase1, single centre, dose-escalating, placebo-controlled study on a genetically modified B. pertussis strain given as a single intranasal dose to healthy adult male volunteers. Effective vaccines are needed to protect young infants (from 0 to 6 months, today the most vulnerable age group), preferably after a single administration very early in life. The successful outcome of this project would constitute an important milestone towards nasal vaccination of infants, possibly at birth with a novel, single-dose pertussis vaccine. Our ultimate aim is to protect infants in the most vulnerable age group, before the regular vaccination schedule using already available vaccines is applied. The ultimate aim is thus not to replace current vaccination schedules with available vaccines, but to add a first nasal vaccination to protect very early in life.

Timeline

Start
2010-08
Primary completion
2011-06
Completion
2012-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject BPZE1 Vaccine 1000 unknown Intranasal
Subject BPZE1 Vaccine 100000 unknown Intranasal
Subject BPZE1 Vaccine 1e+07 unknown Intranasal

Indications