drugset / Trial / NCT00505271

Safety and Efficacy Study Using Rexin-G for Breast Cancer

NCT00505271 ↗

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

Summary

The goal of the adaptive trial design is to confirm the over-all safety 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 for recurrent or metastatic breast cancer.

Timeline

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

Drugs

EvaluationDrugModalityDoseRoute
Subject Rexin-G Unknown — —

Indications