drugset / Trial / NCT00764166

A Prospective Randomized Phase III Study Comparing Hormonal Therapy +/-Docetaxel

NCT00764166

RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective was to evaluate the PSA (biochemical) progression-free survival (PFS) of high-risk metastasis-free PC patients, treated with LH-RH agonist for one year with or without docetaxel after prior radical prostatectomy (RP) or radiotherapy (RT). The study was powered at 80% to detect a 25% improvement in biochemical PFS for a total sample size estimated at 252 patients, with a two-sided type I error rate of 5% (non-parametric methods.

Timeline

Start
2003-06
Primary completion
2009-11
Completion
2010-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule 70 mg/m2 Intravenous
Background Bicalutamide Other / unclassified Oral
Background Triptorelin Other / unclassified Other