CompletedPhase 3NCT00404924
Official study title

ZD6474 (ZACTIMA™) Phase III Study in EGFR Failures

Study summary

This study is being carried out to assess if adding ZD6474 to best supportive care (BSC) is more effective than best supportive care alone, for the treatment of patients with non-small cell lung cancer, whose disease has recurred after previous chemotherapy and an Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor (EGFR TKI). ZD6474 is a new anti-cancer drug in development that works in a different way to standard chemotherapy drugs. It targets the growth of new blood vessels to a tumour and thereby might slow the rate at which the tumour may grow. Early studies indicate that ZD6474 has a positive effect on the time that a tumour may take to progress to a further stage. Approximately 930 patients will take part in this study. It will be conducted in hospitals and clinics in North and South America, Europe and Asia.

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Key things to know

Main goalTreatment

This describes the study’s primary purpose.

What is being studiedZD6474 (vandetanib) and Best Supportive Care

The study team can explain what participation involves.

Who it may be forNon-small cell lung cancer (NSCLC) · EGFR

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Sep 30, 2016 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Phase 3

Interventional

Where is it offered?102 U.S. locations

Locations may change over time.

Who runs it?Genzyme, a Sanofi Company

Study sponsor

01
Study overview

What this study is about

Purpose
Treatment
Study type
Interventional
Phase
Phase 3
Sponsor
Genzyme, a Sanofi Company
Interventions being studied
Drug: ZD6474 (vandetanib); Other: Best Supportive Care
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria

Patients with Non-small cell lung cancer for which the standard cancer treatments of surgery, chemotherapy, radiation or other anticancer drugs are no longer appropriate treatments for you.

Reasons someone may not be able to joinExclusion criteria
  • Patients who have had standard cancer treatments of surgery, chemotherapy or other systemic anti-cancer therapy within 4 weeks before start of study therapy.
  • Three or more prior chemotherapy regimens.
  • Significant cardiovascular events.

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Research SiteTucson, Arizona
  • Research SiteGermantown, Tennessee
  • Research SiteBahía Blanca
  • Research SiteCiudad de Buenos Aires
  • Research SiteLa Plata
  • Research SiteRosario
  • Research SiteSan Miguel de Tucumán
  • Research SiteSanta Fe
  • Research SiteFitzroy
  • Research SitePerth
  • Research SiteSt Leonards
  • Research SiteTugan

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Sep 30, 2016. Always confirm current availability with the study team.

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