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Clinical Trial Summary

This study is a clinical trial phase I/II. Its goal is to determine the safety, tolerability, immunogenicity and efficacy of a therapeutic vaccine with the tumor antigen NY-ESO-1 combined with the adjuvant MPLA from B. pertussis in cancer patients.


Clinical Trial Description

The safety and immunogenicity of the vaccine with the antigen NY-ESO-1 in combination with the MPLA will be evaluated in a phase 1 clinical trial conducted in patients with malignancies that express the antigen (lung, ovarian and melanoma). This study will involve 15 patients, who will receive 250 mcg of NY-ESO-1 and 100 mcg of MPLA. ;


Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01584115
Study type Interventional
Source Instituto de Investigação em Imunologia
Contact Pedro Giavina-Bianchi, PhD,MD
Phone (5511) 26616098
Email pbianchi@usp.br
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date July 2012
Completion date July 2013