A phase 1, randomized, double-blind, placebo-controlled, dose-escalating study to evaluate safety, tolerability, and immunogenicity of leish-111f + MPL-SE vaccine in combination with pentavalent antimony in treatment of mucosal leishmaniasis.

Trial Profile

A phase 1, randomized, double-blind, placebo-controlled, dose-escalating study to evaluate safety, tolerability, and immunogenicity of leish-111f + MPL-SE vaccine in combination with pentavalent antimony in treatment of mucosal leishmaniasis.

Completed
Phase of Trial: Phase I

Latest Information Update: 24 Mar 2009

At a glance

  • Drugs LEISH-F3 peptide vaccine (Primary) ; Monophosphoryl lipid A (Primary) ; Antiprotozoals
  • Indications Leishmaniasis
  • Focus Adverse reactions
  • Most Recent Events

    • 17 Oct 2005 New trial record.
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