Iressa in Poor Performance Status Patients With Previously Untreated Advanced Non-Small Cell Lung Cancer
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT00193336 |
Recruitment Status :
Completed
First Posted : September 19, 2005
Last Update Posted : May 3, 2011
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Lung Cancer | Drug: ZD1839 | Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Enrollment : | 60 participants |
Allocation: | Non-Randomized |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Phase II Trial of Single Agent ZD1839 (Iressa) in Poor Performance Status Patients With Previously Untreated Advanced Non-Small Cell Lung Cancer |
Study Start Date : | March 2003 |
Actual Primary Completion Date : | March 2004 |
Actual Study Completion Date : | September 2005 |

- Overall response rate
- Overall toxicity
- Quality of life

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
To be included in this study, you must meet the following criteria:
- Biopsy proven non-small cell lung cancer
- Recurrent non-small cell lung cancer after previous surgery or radiation
- Advanced disease (stage IIIb or IV)
- No previous chemotherapy or biological therapy
- Require significant assistance with activities of daily living
- Measurable disease
- Adequate bone marrow, liver and kidney function
- Give written informed consent
Exclusion Criteria:
You cannot participate in this study if any of the following apply to you:
- Brain metastasis
- Meningeal metastasis
- Other uncontrolled malignancies
- Women pregnant or lactating
- No measurable disease outside previous radiation therapy field
Please note: There are additional inclusion/exclusion criteria. The study center will determine if you meet all of the criteria. If you do not qualify for the trial, study personnel will explain the reasons. If you do qualify, study personnel will explain the trial in detail and answer any questions you may have.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00193336
Principal Investigator: | John D. Hainsworth, MD | SCRI Development Innovations, LLC |
Publications of Results:
Responsible Party: | SCRI Oncology Research Consortium, SCRI |
ClinicalTrials.gov Identifier: | NCT00193336 |
Other Study ID Numbers: |
SCRI LUN 71 IRUSIRES0002 |
First Posted: | September 19, 2005 Key Record Dates |
Last Update Posted: | May 3, 2011 |
Last Verified: | May 2011 |
NSCLC Lung Cancer Non Small Cell Lung Cancer |
Lung Neoplasms Carcinoma, Non-Small-Cell Lung Respiratory Tract Neoplasms Thoracic Neoplasms Neoplasms by Site Neoplasms Lung Diseases Respiratory Tract Diseases |
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