drugset / Trial / NCT01234025

Safety and Tolerability Study of ISIS EIF4E Rx in Combination With Docetaxel and Prednisone (CRPC)

NCT01234025

Phase 1/2 Completed 113 enrolled Ionis Pharmaceuticals, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to examine the safety, tolerability and progression-free survival of patients with Castrate-Resistant Prostate Cancer treated with ISIS EIF4E Rx in combination with docetaxel and prednisone.

Timeline

Start
2010-11
Primary completion
2013-05
Completion
2013-12

Drugs

EvaluationDrugModalityDoseRoute
Subject ISIS EIF4E Rx Unknown 800 mg Intravenous
Subject ISIS EIF4E Rx Unknown 1000 mg Intravenous
Background Docetaxel Small molecule 75 mg/m2 Intravenous
Background Prednisone Other / unclassified 5 mg Oral