drugset / Trial / NCT01885702

Dendritic Cell Vaccination in Patients With Lynch Syndrome or Colorectal Cancer With MSI

NCT01885702

Phase 1/2 Unknown 25 enrolled Radboud University Medical Center
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Objectives: In this Radboud University Nijmegen Medical Centre (RUNMC) initiated study our first objective is to investigate toxicity (safety and feasibility) of vaccination with frameshift-derived neoantigen-loaded DC of CRC patients with an MSI-positive CRC and persons who are known to be carrier of a germline MMR-gene mutation with no signs of disease yet. The secondary objectives of the study are: * to demonstrate that peptide-loaded DC can induce or enhance an immune response to tumor-associated antigen CEA and specific frameshift-derived neoantigens in the study population. * to study the pathological and clinical responses, e.g. disease-free survival, determined according to the standard protocol. Study design: This study is a phase I/II open-label study. Study population: Two groups of adults will be vaccinated: Group I) CRC patients, who are known to carry a germline MMR-gene mutation and patients with an MSI-positive CRC and yet unknown or negative MMR-gene mutation status. Group II) persons who are known to be carrier of a germline MMR-gene mutation with no signs of disease yet. All participants need to be HLA-A2.1 positive.

Timeline

Start
2010-10
Primary completion
2016-04
Completion
2025-09

Drugs

EvaluationDrugModalityDoseRoute
Subject DCVax-L Vaccine

Indications