Clinical trial

Docetaxel in Hormone Refractory Prostate Cancer (HRPC)[Weekly or 3weekly TAX +…

NCT00268710 · Sanofi, Industry · Completed

Key facts

NCT number NCT00268710
Title Docetaxel in Hormone Refractory Prostate Cancer (HRPC)[Weekly or 3weekly TAX + Prednisone in HRPC]
Official title Multicenter Phase II Study of Taxotere (Docetaxel) Administered Weekly or Every Three Weeks in Combination With Prednisone as Second Line Chemotherapy in Patients With Hormone Refractory Prostate Cancer (HRPC)
Lead sponsor Sanofi, Industry
Collaborators Canadian Urologic Oncology Group
Status Completed
Phase Phase 2
Study type Interventional
Conditions Prostatic Neoplasms
Intervention type Drug
Interventions docetaxel
Start date Feb 1, 2004
Primary completion Mar 1, 2006
Completion Mar 1, 2006
First posted Dec 22, 2005
Last update posted Dec 7, 2009

At a glance

  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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