drugset / Trial / NCT00946881

Safety and Tolerability Study Using WST11 In Patients With Localized Prostate Cancer

NCT00946881 ↗

Phase 1/2 Completed 30 enrolled Steba Biotech S.A.
NaSingle-groupOpen-labelTreatment

Summary

The aim of this study is to determine the optimal treatment conditions (WST11 dose and light energy dose) to achieve ablation in one lobe of the prostate and to evaluate the safety and quality of life of WST11 medicated Vascular-Targeted Photodynamic therapy (VTP) in men with localized prostate cancer.

Timeline

Start
2009-07
Primary completion
2012-07
Completion
2012-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Padeliporfin Other / unclassified 2 mg/kg Intravenous
Subject Padeliporfin Other / unclassified 4 mg/kg Intravenous
Subject Padeliporfin Other / unclassified 6 mg/kg Intravenous

Indications