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A Phase 2, Randomized, Open-Label, Controlled Study to Evaluate the Efficacy, Safety, and Immunogenicity of the LEISH-F2 + MPL-SE Vaccine in the Treatment of Patients With Cutaneous Leishmaniasis.

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Trial Profile

A Phase 2, Randomized, Open-Label, Controlled Study to Evaluate the Efficacy, Safety, and Immunogenicity of the LEISH-F2 + MPL-SE Vaccine in the Treatment of Patients With Cutaneous Leishmaniasis.

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 02 May 2023

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At a glance

  • Drugs LEISH-F3 peptide vaccine (Primary) ; Monophosphoryl lipid A (Primary) ; Sodium stibogluconate
  • Indications Cutaneous leishmaniasis
  • Focus Adverse reactions; Registrational; Therapeutic Use

Most Recent Events

  • 26 Dec 2013
  • 24 Jul 2012 Actual end date (1 Dec 2011) added as reported by ClinicalTrials.gov.
  • 01 Dec 2011 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.

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