drugset / Trial / NCT00450970

Expanded Access Study of Satraplatin Plus Prednisone in Patients With Hormone Refractory Prostate Cancer (HRPC)

NCT00450970

Phase 3 Terminated 344 enrolled Agennix
RandomizedSingle-groupOpen-labelTreatment

Summary

The SPERA trial is designed to 1. provide satraplatin to physicians with patients who have hormone refractory prostate cancer (HRPC) which has progressed following unlimited cytotoxic chemotherapy regimens for metastatic disease and 2. to evaluate the safety of oral satraplatin in this patient population.

Timeline

Start
2007-02
Primary completion
2009-03
Completion
2009-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Satraplatin Other / unclassified 80 mg/m2 Oral

Indications