drugset / Trial / NCT07647107

A Phase I Study of Lipovaxin Tuberculosis Vaccine in Adult Healthy Populations

NCT07647107 ↗

RandomizedSequentialQuadruple-blindTreatment

Summary

A Phase I, Double-Blind, Randomized, Placebo Controlled Trial to Evaluate Safety and Immunogenicity of Lipovaxin Tuberculosis Vaccine (Bio Farma) in Healthy Populations Aged 18-40 Years in Indonesia

Timeline

Start
2026-08
Primary completion
2027-07
Completion
2027-08

Drugs

EvaluationDrugModalityDoseRoute
Subject LipovaxinS4-EAH Vaccine 20 ug Intramuscular
Subject LipovaxinS4-EAH Vaccine 25 ug Intramuscular

Indications