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.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
48
Unnamed facility
Los Angeles, California, United States
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Lexington, Kentucky, United States
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Baltimore, Maryland, United States
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Worcester, Massachusetts, United States
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Minneapolis, Minnesota, United States
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St Louis, Missouri, United States
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New York, New York, United States
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Charlotte, North Carolina, United States
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Cleveland, Ohio, United States
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Philadelphia, Pennsylvania, United States
...and 3 more locations
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