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Anti-metabolites
Efficacy Study Comparing ZD6474 in Combination With Pemetrexed and Pemetrexed Alone in 2nd Line NSCLC Patients (ZEAL Trial)
Phase 3
Waitlist Available
Research Sponsored by Genzyme, a Sanofi Company
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up time to death in months
Awards & highlights
Pivotal Trial
Summary
This trial is testing if adding vandetanib to the existing lung cancer drug Alimta (pemetrexed) is more effective for patients with advanced non-small cell lung cancer who have already been treated. Vandetanib helps by blocking signals that allow cancer cells to grow and get blood supply. Vandetanib is taken orally and has been studied for its effectiveness and safety in advanced lung cancer.
Eligible Conditions
- Lung Cancer
- Non-Small Cell Lung Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ time to death in months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~time to death in months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Progression-Free Survival (PFS) in the Female Population
Progression-Free Survival (PFS) in the Overall Population
Secondary study objectives
Disease Control Rate (DCR)
Duration of Response (DoR)
Erythrocyte Indices
+5 moreAwards & Highlights
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: 2Experimental Treatment2 Interventions
Vandetanib + Pemetrexed
Group II: 1Placebo Group1 Intervention
Placebo Vandetanib + Pemetrexed
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Vandetanib
2007
Completed Phase 3
~5790
Pemetrexed
2014
Completed Phase 3
~5550
Find a Location
Who is running the clinical trial?
Genzyme, a Sanofi CompanyLead Sponsor
527 Previous Clinical Trials
185,038 Total Patients Enrolled
Clinical Sciences & OperationsStudy DirectorSanofi
876 Previous Clinical Trials
2,020,972 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are expected to live for at least 12 more weeks.
Research Study Groups:
This trial has the following groups:- Group 1: 1
- Group 2: 2
Awards:
This trial has 1 awards, including:- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.