drugset / Trial / NCT00546273

Clinical Trial to Study 4 Different Doses of the Vaccine RUTI in Healthy Volunteers

NCT00546273 ↗

RandomizedSingle-groupQuadruple-blindTreatment

Summary

The aim of this study is to evaluate the safety of a new vaccine against Tuberculosis (RUTI) when administered to healthy adult volunteers, compared to placebo; and determine its safe dosage range. An initial evaluation of immune responses to the vaccine compared to placebo will also be undertaken. In the present Phase I clinical trial, four increasing doses of RUTI will be tested, the groups composed by 6 volunteers each. (Total of 24 volunteers). The escalation to a new dose to test will be done after the safety of the previous dose has been ensured. For each dose of FCMtb to test, each volunteer will be inoculated twice (at day 0 and day 28) with RUTI (4 volunteers) or placebo (2 volunteers) and will be followed-up up to 25 weeks from the first inoculation. The global length of the study will be approximately 15 months.

Timeline

Start
2007-04
Primary completion
2008-06
Completion
2008-06

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject RUTI Vaccine 5 ug Subcutaneous
Subject RUTI Vaccine 25 ug Subcutaneous
Subject RUTI Vaccine 100 ug Subcutaneous
Subject RUTI Vaccine 200 ug Subcutaneous