Clinical Trials Directory

Trials / Completed

CompletedNCT00633724

Multiple-Vaccine Therapy in Treating Patients With Non-small Cell Lung Cancer

Phase I Study of Multiple-vaccine Therapy Including Antiangiogenic Vaccine Using Epitope Peptide Restricted to HLA-A*2402 in Treating Patients With Unresectable or Recurrent Non-small Cell Lung Cancer

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
9 (estimated)
Sponsor
Fukushima Medical University · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the safety, tolerability, immune response and clinical response of different doses of HLA-A\*2402 restricted epitope peptides URLC10, TTK, VEGFR1 and VEGFR2 emulsified with Montanide ISA 51.

Detailed description

URLC10 and TTK have been identified as cancer specific molecules especially in non small cell lung cancer using genome-wide expression profile analysis by cDNA microarray technique. We have determined the HLA-A\*2402 restricted epitope peptides derived from these molecules. We also tend to use the peptides targeting to tumor angiogenesis. VEGF receptor 1 and 2 are essential targets to tumor angiogenesis, and we identified that peptides derived from these receptors significantly induce the effective tumor specific CTL response in vitro and vivo. According to these findings, in this trial, we evaluate the safety, immunological and clinical response of those peptides.

Conditions

Interventions

TypeNameDescription
BIOLOGICALHLA-A*2402restricted URLC10, TTK, VEGFR1 and VEGFR2Escalating doses of every peptide will be administered by subcutaneous injection on days 1,8,15 and 22 of each 28-day treatment cycles. Planned doses of peptides are 0.5mg, 1.0mg and 3.0mg.

Timeline

Start date
2007-05-01
Primary completion
2012-06-01
Completion
2012-06-01
First posted
2008-03-12
Last updated
2013-08-15

Locations

1 site across 1 country: Japan

Source: ClinicalTrials.gov record NCT00633724. Inclusion in this directory is not an endorsement.