drugset / Trial / NCT02982395

Study to Evaluate the Efficacy and Safety Of Intravesical Nanoxel®M In BCG Refractory NMIBC

NCT02982395

Phase 3 Terminated 36 enrolled Samyang Biopharmaceuticals Corporation
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to determine whether Nanoxel®M is effective in the treatment of patients with recurrent Ta and T1 who experienced treatment failure with at least one prior BCG intravesical treatment.

Timeline

Start
2017-01
Primary completion
2018-08
Completion
2018-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel-PM Unknown 75 mg Other
Comparator Mitomycin C Other / unclassified 40 mg Other