drugset / Trial / NCT01232712

A Study to Assess the Safety and Efficacy of MUC1 Peptide Vaccine and hGM-CSF in Patients With MUC1-positive Tumor Malignancies

NCT01232712

Phase 1/2 Completed 15 enrolled Vaxil Therapeutics Ltd.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The scientific approach behind this study is to develop novel anti-cancer therapeutic vaccine to induce a robust cellular immune response mediated via both CD4+ and CD8+ T lymphocytes populations and can be be applicable to the majority of the target population.

Timeline

Start
2010-09
Primary completion
2013-05
Completion
2013-05

Drugs

EvaluationDrugModalityDoseRoute
Subject ImMucin Peptide 100 ug Subcutaneous
Subject ImMucin Peptide 250 ug Subcutaneous
Background hGM-CSF Protein / enzyme biologic 250 ug

Indications