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LUCY: A Study for the Treatment of Non-Small Cell Lung Cancer (NSCLC) in Patients Previously Treated With Chemotherapy

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00328588
First Posted: May 22, 2006
Last Update Posted: January 2, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Astellas Pharma Inc
May 19, 2006
May 22, 2006
January 2, 2008
December 2006
March 2007   (Final data collection date for primary outcome measure)
Tumor response rate (CR+PR) [ Time Frame: In first 6 cycles ]
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Complete list of historical versions of study NCT00328588 on ClinicalTrials.gov Archive Site
Not Provided
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LUCY: A Study for the Treatment of Non-Small Cell Lung Cancer (NSCLC) in Patients Previously Treated With Chemotherapy
Not Provided
A study for the treatment of Non-Small Cell Lung Cancer (NSCLC) in patients previously treated with chemotherapy.
Not Provided
Interventional
Phase 2
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
  • Lung Cancer
  • Cancer of Lung
  • Cancer of the Lung
  • Non-Small Cell Lung Carcinoma
  • Carcinoma, Non-Small Cell Lung
Drug: YM155
IV
Experimental: 1
7 days continuous infusion
Intervention: Drug: YM155
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
37
March 2007
March 2007   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Histologically or cytologically confirmed non-small cell lung cancer.
  • Prior chemotherapy regimen(s) for lung cancer

Exclusion Criteria:

  • History of other malignancy in the last 5 years
  • Major surgery within the past 21 days
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Czech Republic,   Germany,   Netherlands
 
 
NCT00328588
155-CL-006
Not Provided
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Disclosure Office Europe, Astellas Pharma Europe BV
Astellas Pharma Inc
Not Provided
Study Director: Medical Director Astellas Pharma Europe B.V.
Astellas Pharma Inc
December 2007

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