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A Phase IIa. Open-label, Multicenter, Dose-escalation Study to Assess the Tolerability and Pharmacokinetics of ZD4054 Given Orally Once Daily in Subjects With Metastatic Prostate Cancer
This study has been completed.
Study NCT00055471   Information provided by AstraZeneca
First Received: March 3, 2003   Last Updated: October 20, 2009   History of Changes

March 3, 2003
October 20, 2009
 
 
 
 
Complete list of historical versions of study NCT00055471 on ClinicalTrials.gov Archive Site
 
 
 
A Phase IIa. Open-label, Multicenter, Dose-escalation Study to Assess the Tolerability and Pharmacokinetics of ZD4054 Given Orally Once Daily in Subjects With Metastatic Prostate Cancer
 

The primary purpose of this study is to determine the safest dose of ZD4054 in men with prostate cancer

 
Phase II
Interventional
Treatment
  • Prostatic Neoplasms
  • Metastases, Neoplasm
Drug: ZD4054
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
 
 
 

Inclusion Criteria:

  • Men 18 years & older
  • Confirmed diagnosis of prostate cancer with bone metastases

Exclusion Criteria:

  • No more than 2 prior chemotherapy regimens
  • No radiation, chemotherapy or bisphosphonates in the past 4 weeks
Male
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00055471
 
4054IL/0004
AstraZeneca
 
 
AstraZeneca
October 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP