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Carcinoma, Non-Small-Cell LungPhase 2NCT00071188

ZD6474 Alone or in Combination With Paclitaxel and Carboplatin in Subjects With Previously Untreated Locally Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC)

A Phase 2 study testing ZD6474, Paclitaxel and Carboplatin in people with Carcinoma, Non-Small-Cell Lung, run by Genzyme, a Sanofi Company at 34 sites in 9 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of the run-in phase of this study is to determine the appropriate and tolerable dose of ZD6474 (200mg or 300mg) to be administered in combination with paclitaxel and carboplatin in subjects with previously untreated locally advanced or metastatic NSCLC. This phase of the trial is closed to enrollment. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Carcinoma, Non-Small-Cell Lung
What is being tested?
ZD6474, Paclitaxel and Carboplatin
How many people
Not given
Where
34 sitesin 9 countries
Study dates
Feb 2004to Oct 2007
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Signed informed consent
  • 18 years or older
  • Histologically or cytologically confirmed locally advanced or metastatic NSCLC
  • No prior chemotherapy/biological therapy/radiation therapy
  • One or more measurable lesions
  • Life expectancy more than 12 weeks

Who cannot join

  • Brain metastases or spinal cord compression
  • Currently active skin disease
  • History of significant hemoptysis
  • Abnormal blood chemistry
  • Cardiac abnormalities
  • Recent significant cardiac event
  • Coexisting malignancies

Trial locations and contacts

34 sites in 9 countries.

34 sites in 9 countries

United States12 sites
  • Research Site

    Austin, Texas

  • Research Site

    Boston, Massachusetts

  • Research Site

    Chicago, Illinois

  • Research Site

    Concord, California

  • Research Site

    Houston, Texas

  • Research Site

    Los Angeles, California

  • Research Site

    Lubbock, Texas

  • Research Site

    Nashville, Tennessee

  • Research Site

    Norfolk, Virginia

  • Research Site

    Providence, Rhode Island

  • Research Site

    Seattle, Washington

  • Research Site

    St Louis, Missouri

Other trials in United States

South Africa5 sites
  • Research Site

    Cape Town

  • Research Site

    Johannesburg

  • Research Site

    Panorama

  • Research Site

    Parkland

  • Research Site

    Pretoria

Other trials in South Africa

Germany4 sites
  • Research Site

    Essen

  • Research Site

    Frankfurt

  • Research Site

    Mainz

  • Research Site

    Ulm

Other trials in Germany

Spain4 sites
  • Research Site

    Barcelona

  • Research Site

    Madrid

  • Research Site

    Málaga

  • Research Site

    Pamplona

Other trials in Spain

France3 sites
  • Research Site

    Besançon

  • Research Site

    Lille

  • Research Site

    Strasbourg

Other trials in France

Finland2 sites
  • Research Site

    Helsinki

  • Research Site

    Turku

Other trials in Finland

Italy2 sites
  • Research Site

    Milan

  • Research Site

    Orbassano

Other trials in Italy

India1 site
  • Research Site

    Pune

Other trials in India

Thailand1 site
  • Research Site

    Chiang Mai

Other trials in Thailand

About this study

Official title: A Randomized, Partially Blinded, Phase II Study to Assess the Safety, Tolerability and Efficacy of ZD6474 Alone or in Combination With Paclitaxel and Carboplatin in Subjects With Previously Untreated Locally Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC)

The purpose of the run-in phase of this study is to determine the appropriate and tolerable dose of ZD6474 (200mg or 300mg) to be administered in combination with paclitaxel and carboplatin in subjects with previously untreated locally advanced or metastatic NSCLC. This phase of the trial is closed to enrollment.

The purpose of the randomized phase of this study is to determine the efficacy of ZD6474 alone versus that of ZD6474 in combination with paclitaxel and carboplatin versus that of paclitaxel and carboplatin alone in subjects with previously untreated locally advanced or metastatic NSCLC. This phase of the trial is closed to enrollment.

Being tested
ZD6474, Paclitaxel, Carboplatin
Keywords
Non-Small-Cell Lung Carcinoma
Medical subject headings
Carcinoma, Non-Small-Cell Lung

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Oct 2003 (estimated)
  2. Study startFeb 2004
  3. Primary completionOct 2007
  4. Study completionOct 2007

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
IDs, dates and publications
ClinicalTrials.gov ID
NCT00071188
Sponsor's protocol ID
D4200C00007
Other IDs
D4200C00007(run-in), D4200C0007A (randomization)
Status last verified
Aug 2016
First submitted
14 Oct 2003
Last updated
25 Aug 2016
Results posted
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing ZD6474, Paclitaxel and Carboplatin in people with Carcinoma, Non-Small-Cell Lung, run by Genzyme, a Sanofi Company at 34 sites in 9 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 25 Aug 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 34 sites in United States, South Africa, Germany, Spain, France and 4 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Aug 2016; AzTrials last refreshed its copy on 7 Nov 2026.

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