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Phase 2 Study of TLK286 Administered Weekly in Advanced Non-Small Cell Lung Cancer
This study has been completed.
Study NCT00040638   Information provided by Telik
First Received: July 2, 2002   Last Updated: January 10, 2008   History of Changes

July 2, 2002
January 10, 2008
 
 
 
 
Complete list of historical versions of study NCT00040638 on ClinicalTrials.gov Archive Site
 
 
 
Phase 2 Study of TLK286 Administered Weekly in Advanced Non-Small Cell Lung Cancer
 

The purpose of this study is to determine the effectiveness of TLK286 in the treatment of advanced non-small cell lung cancer.

 
Phase II
Interventional
Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Carcinoma, Non-Small-Cell Lung
Drug: TLK286
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
40
 
 

Inclusion Criteria:

  • Histologic or cytologic diagnosis of non-small cell lung carcinoma
  • Progressed while on or after treatment on platinum-based regimen
  • Patients may not have had more than one prior cytotoxic chemotherapy regimen
  • Stage IV or IIIB
  • Age at least 18 years
  • Adequate liver and kidney function
  • Adequate bone marrow function

Exclusion Criteria:

  • Pregnancy or lactation
  • Unstable medical conditions
  • Chemotherapy, hormonal therapy, radiotherapy, radiopharmaceuticals or immunotherapy within 3 weeks of TLK286
  • CNS metastasis unless controlled by treatment
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00040638
 
TLK286.2014
Telik
 
 
Telik
February 2007

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