drugset / Trial / NCT00764166
A Prospective Randomized Phase III Study Comparing Hormonal Therapy +/-Docetaxel
Phase 3
Unknown
254 enrolled
Assistance Publique - Hôpitaux de Paris
ARTIC group (oncologists and urologists association) · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Docetaxel | Small molecule | 70 mg/m2 | Intravenous |
| Background | Bicalutamide | Other / unclassified | — | Oral |
| Background | Triptorelin | Other / unclassified | — | Other |