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Study of TLK286 (Telcyta) vs. Gefitinib in Locally Advanced or Metastatic Non-Small Cell Lung Cancer
This study has been completed.
First Received: March 26, 2004   Last Updated: January 10, 2008   History of Changes
Sponsor: Telik
Information provided by: Telik
ClinicalTrials.gov Identifier: NCT00080340
  Purpose

The purpose of this study is to determine if TLK286(Telcyta) is more effective than gefitinib (Iressa) in the treatment of non-small cell lung cancer.


Condition Intervention Phase
Non Small Cell Lung Carcinoma
Drug: TLK286 (Telcyta) HCl for Injection
Drug: gefitinib (Iressa)
Phase III

Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title: Phase 3 Randomized Study of TLK286 (Telcyta) Versus Gefitinib (Iressa) as Third-Line Therapy in Locally Advanced or Metastatic Non-Small Cell Lung Cancer

Resource links provided by NLM:


Further study details as provided by Telik:

Estimated Enrollment: 520
Estimated Study Completion Date: May 2005
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Clinical diagnosis of non-small cell lung cancer
  • Non-small cell lung cancer that is not curable with surgery, radiation, or combined modality chemoradiation
  • Failed two prior chemotherapy regimens which must have included platinum
  • Measurable disease

Exclusion Criteria:

  • Treatment with more than two prior chemotherapy regimens
  • History of bone marrow transplantation or stem cell support
  • Pregnant or lactating women
  • Known history of prior gefitinib therapy
  • Known history of prior TLK286 therapy
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00080340

  Show 345 Study Locations
Sponsors and Collaborators
Telik
  More Information

Additional Information:
No publications provided

Study ID Numbers: TLK286.3020
Study First Received: March 26, 2004
Last Updated: January 10, 2008
ClinicalTrials.gov Identifier: NCT00080340     History of Changes
Health Authority: United States: Food and Drug Administration

Additional relevant MeSH terms:
Thoracic Neoplasms
Respiratory Tract Neoplasms
Neoplasms by Histologic Type
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents
Enzyme Inhibitors
Protein Kinase Inhibitors
Pharmacologic Actions
Carcinoma
Neoplasms
Neoplasms by Site
Respiratory Tract Diseases
Lung Neoplasms
Therapeutic Uses
Lung Diseases
Carcinoma, Non-Small-Cell Lung
Gefitinib
Neoplasms, Glandular and Epithelial

ClinicalTrials.gov processed this record on November 30, 2009