Lung Cancer Clinical Trial

Study Evaluating MAC-321 in Non-small Cell Lung Cancer Refractory to Platinum-based Therapy

Summary

This non-randomized, open-label clinical trial is designed to determine safety and clinical activity of a new chemotherapeutic agent, MAC-321, when given intravenously to patients with non-small cell lung cancer. Clinical activity will be evaluated by determining the percentage of patients with an objective tumor response after treatment with MAC-321. Patients must have been previously treated with a platinum-containing chemotherapy regimen.

A total of 96 patients will be enrolled in this trial. Eligible patients will receive MAC-321 intravenously every 3 weeks for up to a total of 6 courses of treatment. All patients will receive MAC-321 at the same dose. MAC-321 is an experimental drug, and is not offered outside of this research trial.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Recurrence of non-small cell lung cancer after at least 1 prior chemotherapy regimen containing a platinum agent
Recovery from all acute side effects of prior therapies (with the exception of hair loss)
Adequate bone marrow, liver, and kidney function

Exclusion Criteria:

More than 2 prior chemotherapy regimens for treatment of advanced or metastatic non-small cell lung cancer. (Treatment given in conjunction with surgery will not be included in the maximum of 2 prior regimens)
Radiation therapy, chemotherapy or any other anticancer therapy within 28 days of beginning study
Symptomatic brain metastases

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

48

Study ID:

NCT00063219

Recruitment Status:

Completed

Sponsor:

Wyeth is now a wholly owned subsidiary of Pfizer

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There are 13 Locations for this study

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Los Angeles California, 90033, United States

Lexington Kentucky, 40536, United States

Baltimore Maryland, 21231, United States

Worcester Massachusetts, 01655, United States

Minneapolis Minnesota, 55455, United States

St. Louis Missouri, 63110, United States

New York New York, 10032, United States

Charlotte North Carolina, 28203, United States

Cleveland Ohio, 44195, United States

Philadelphia Pennsylvania, 19140, United States

Pittsburgh Pennsylvania, 15213, United States

Charleston South Carolina, 29425, United States

Nashville Tennessee, 37232, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 2

Estimated Enrollment:

48

Study ID:

NCT00063219

Recruitment Status:

Completed

Sponsor:


Wyeth is now a wholly owned subsidiary of Pfizer

How clear is this clinincal trial information?

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