drugset / Trial / NCT02729571

Dose-escalation Safety and Immunogenicity Study to Compare MTBVAC to BCG in Newborns With a Safety Arm in Adults

NCT02729571 ↗

RandomizedParallel-groupQuadruple-blindPrevention

Summary

Randomized, controlled, double blind clinical trial in 2 stages (adult stage, infant stage). The first stage includes 18 HIV uninfected, QFT negative, BCG vaccinated, adult participants, randomized 1:1 to receive BCG Vaccine SSI or MTBVAC at equivalent dose (5x10E05 CFU/0.1mL) (n=9 in each group). Upon favourable safety review by the DSMB for all 18 adults up to day 28 after study vaccination, the second stage will commence in thirty-six (36) HIV unexposed, BCG naïve, newborn infants, randomized 1:3 to receive BCG Vaccine SSI or MTBVAC at one of three different dose levels ( (n=9 in each group).

Timeline

Start
2015-09
Primary completion
2016-09
Completion
2018-03

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator BCG Vaccine SSI Unknown 250000 unknown Other
Comparator BCG Vaccine SSI Unknown 500000 unknown Other
Subject MTBVAC Vaccine 2500 unknown Other
Subject MTBVAC Vaccine 25000 unknown Other
Subject MTBVAC Vaccine 250000 unknown Other
Subject MTBVAC Vaccine 500000 unknown Other

Indications