drugset / Trial / NCT03200821

An Open Label Study to Evaluate G17DT Compared to Gemcitabine

NCT03200821

Phase 3 Completed 103 enrolled Cancer Advances Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

In this study 250 µg of G17DT was administered at Weeks 0, 2 and 6 in order to demonstrate non inferiority compared to gemcitabine in prolonging survival in advanced pancreatic cancer.

Timeline

Start
2000-08-14
Primary completion
2001-09-24
Completion
2002-09-19

Drugs

EvaluationDrugModalityDoseRoute
Subject G17DT Immunogen Vaccine 250 ug Intramuscular
Comparator Gemcitabine Small molecule 1000 ug/m2 Intravenous