Viewing Study NCT00006048



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Last Modification Date: 2024-10-26 @ 9:05 AM
Study NCT ID: NCT00006048
Status: UNKNOWN
Last Update Posted: 2013-12-19
First Post: 2000-07-05

Brief Title: ZD 1839 Plus Combination Chemotherapy in Treating Patients With Non-Small Cell Lung Cancer
Sponsor: AstraZeneca
Organization: National Cancer Institute NCI

Study Overview

Official Title: A Randomized Double Blind Phase III Comparative Trial of 2 Doses of ZD1839 IRESSA in Combination With Gemcitabine and Cisplatin Versus Placebo in Combination With Gemcitabine and Cisplatin in Chemotherapy Naive Patients With Advanced Stage III or IV Non-Small Cell Lung Cancer
Status: UNKNOWN
Status Verified Date: 2001-07
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: RATIONALE Some tumors need growth factors produced by the bodys white blood cells to keep growing ZD 1839 may interfere with the growth factor and stop the tumor from growing Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die It is not yet known whether chemotherapy is more effective with or without ZD 1839 for non-small cell lung cancer

PURPOSE Randomized phase III trial to compare the effectiveness of combination chemotherapy with or without ZD 1839 in treating patients who have stage IIIB or stage IV non-small cell lung cancer
Detailed Description: OBJECTIVES I Compare the 1 year survival rate time to worsening of disease related symptoms and progression free survival in chemotherapy naive patients with stage IIIB or IV non-small cell lung cancer treated with one of two doses of ZD 1839 or placebo combined with gemcitabine and cisplatin

OUTLINE This is a randomized double blind placebo controlled multicenter study Patients are randomized to one of three treatment arms Patients receive gemcitabine and cisplatin combined with lower dose oral ZD 1839 arm I higher dose oral ZD 1839 arm II or placebo arm III

PROJECTED ACCRUAL A total of 1029 patients 343 per arm will be accrued for this study

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
ZENECA-1839IL0014 None None None