drugset / Trial / NCT00504998

Safety/Efficacy Study of Rexin-G to Treat Pancreatic Cancer

NCT00504998 ↗

Phase 1/2 Completed 20 enrolled Epeius Biotechnologies
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The goal of the adaptive trial design is to determine the over-all safety of escalating doses of Rexin-G and to determine the optimal dosing regimen for Rexin-G that would document the significant clinical benefits required to support a Phase II registration protocol.

Timeline

Start
2007-07
Primary completion
2010-07
Completion
2011-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Rexin-G Unknown 1e+11 unknown Intravenous
Subject Rexin-G Unknown 2e+11 unknown Intravenous
Subject Rexin-G Unknown 3e+11 unknown Intravenous
Subject Rexin-G Unknown 4e+11 unknown Intravenous