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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00080340
Registration number
NCT00080340
Ethics application status
Date submitted
26/03/2004
Date registered
30/03/2004
Date last updated
15/01/2008
Titles & IDs
Public title
Study of TLK286 (Telcyta) vs. Gefitinib in Locally Advanced or Metastatic Non-Small Cell Lung Cancer
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Scientific 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
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Secondary ID [1]
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TLK286.3020
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Non Small Cell Lung Carcinoma
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Condition category
Condition code
Cancer
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Lung - Non small cell
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
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Comparator / control treatment
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Control group
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Outcomes
Eligibility
Key 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
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key 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
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Other reasons
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Sample size
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC
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Recruitment hospital [1]
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Albury Base Hospital - Albury
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West Albury Barker's Pharmacy - Albury
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Department of Medical Oncology-Newcastle Mater Misericordiae Hospital - Waratah
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Department Of Oncology - South Brisbane
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Flinders Medical Centre - Bedford Park
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St. Vincent's Hospital - Fitzroy
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Pharmatel Fresenius Kabi Pty Ltd. - West Melbourne
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Murray Valley Private Hospital - Wodonga
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Bankstown Lidcombe Hospital - Department of Medical Oncology - Bankstown
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Royal Hobart Hospital - Hobart
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Sir Charles Gairdner Hospital - Nedlands
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Royal North Shore Hospital-Medical Oncology Dept. - St. Leonards
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Border Medical Oncology - Murray Valley Private Hospital - Wodonga
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Clinical Trials Centre - Wollongong Hospital - Wollongong
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2640 - Albury
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2298 - Waratah
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4101 - South Brisbane
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5041 - Bedford Park
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3065 - Fitzroy
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3003 - West Melbourne
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3690 - Wodonga
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2200 - Bankstown
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7000 - Hobart
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6009 - Nedlands
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2065 - St. Leonards
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2500 - Wollongong
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Telik
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Address
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Ethics approval
Ethics application status
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Summary
Brief summary
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.
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Trial website
https://clinicaltrials.gov/study/NCT00080340
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Contacts
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT00080340
Download to PDF