CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 1,494 enrolled
Drug / intervention
Docetaxel +2 moredrug
Likely dose
ZD4054 10 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00617669
NCT00617669Phase 3Completed

A Phase III, Randomised, Double-blind, Placebo-controlled Study to Assess the Efficacy and Safety of 10 mg ZD4054 (Zibotentan) in Combination With Docetaxel in Comparison With Docetaxel in Patients With Metastatic Hormone-resistant Prostate Cancer

AstraZeneca·interventional·Posted Feb 18, 2008·Updated Sep 10, 2012

In Brief

A Phase 3 clinical trial evaluating Docetaxel, ZD4054, and 1 other intervention for Prostate Cancer. Completed, enrolled 1,494 participants across 147 sites in 26 countries.

Detailed Summary

Enthuse M1C is a large phase III clinical trial studying the safety and efficacy of ZD4054 (Zibotentan) in combination with docetaxel (Taxotere) in patients with metastatic hormone resistant prostate cancer (HRPC). This clinical trial will test if the Endothelin A Receptor Antagonist ZD4054 (Zibotentan) can further improve survival compared with docetaxel alone. ZD4054 (Zibotentan) is a new type of agent, which is thought to slow tumour growth and spread by blocking Endothelin A receptor activity. This trial will look at the effects of ZD4054 (Zibotentan) in hormone resistant prostate cancer patients with bone metastases compared with docetaxel. All patients participating in this clinical trial will receive docetaxel chemotherapy, which is a commonly used chemotherapy to treat prostate cancer in addition to other existing prostate cancer therapies. Half the patients will receive ZD4054 (Zibotentan), and half the patients will receive placebo in addition to docetaxel and other prostate cancer therapy. By participating in this trial there is a 50% chance that patients will receive an agent that may further slow the progression of the tumour. No patients will be deprived of standard prostate cancer therapy.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsProstate Cancer
CountriesArgentina, Australia, Brazil, Canada, Czechia, Finland, France, Germany, Hungary, India, Italy, Netherlands, Peru, Poland, Portugal, Romania, Russia, Serbia, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedFeb 18, 2008
Enrollment StartJan 1, 2008
Primary CompletionMay 1, 2011
Study CompletionJul 1, 2011
TodayJul 2, 2026
Enrollment to primary: 3.3 yearsPosted 18.4 years ago

Interventions

Docetaxeldrug

intravenous infusion given every three weeks

ZD4054drug

10 mg oral once daily dose

Placebodrug

placebo oral tablet once daily