Clinical Trials Directory

Trials / Completed

CompletedNCT00059722

This Study is to Compare the Efficacy of ZD6474 and ZD1839 in Subjects With NSCLC.

A Phase II, Randomized Double-blind, 2-part, Multicenter Study to Compare the Efficacy of ZD6474 With the Efficacy of ZD1839 (Iressa™) in Subjects With Locally Advanced or Metastatic (IIIB/IV) Non-small Cell Lung Cancer After Failure of First-line Platinum-based Chemotherapy and to Assess the Activity of ZD6474 in Subjects Following Failure of Treatment With ZD1839.

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
160 (planned)
Sponsor
Genzyme, a Sanofi Company · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the efficacy of ZD6474 and ZD1839 in patients with NSCLC after Failure of Prior Platinum-based Chemotherapy.

Conditions

Interventions

TypeNameDescription
DRUGZD6474
DRUGPlacebo
DRUGZD1839

Timeline

Start date
2003-05-01
Completion
2007-06-01
First posted
2003-05-05
Last updated
2016-08-24

Locations

48 sites across 6 countries: United States, Argentina, Belgium, Germany, South Africa, United Kingdom

Source: ClinicalTrials.gov record NCT00059722. Inclusion in this directory is not an endorsement.

This Study is to Compare the Efficacy of ZD6474 and ZD1839 in Subjects With NSCLC. (NCT00059722) · Clinical Trials Directory