drugset / Trial / NCT00121862

Study to Evaluate the Leish-111f + MPL-SE Vaccine in Healthy Adults Not Previously Exposed to Leishmania Parasite

NCT00121862

RandomizedParallel-groupDouble-blindPrevention

Summary

This study will evaluate the safety and immunogenicity of the Leish-111f + MPL-SE vaccine in adult subjects who have no evidence of previous exposure to the Leishmania parasite.

Timeline

Start
2005-08
Primary completion
Completion
2006-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Leish-111f Protein / enzyme biologic 10 ug
Background MPL-SE Other / unclassified 25 ug