Lung Cancer Clinical Trial

A Study of Motexafin Gadolinium (MGd) in Combination With Docetaxel and Cisplatin for Treatment of Non-Small Cell Lung Cancer (NSCLC)

Summary

The purpose of the study is to determine the dose limiting toxicities and maximum tolerated dose of motexafin gadolinium when administered with docetaxel and cisplatin in patients with Non-small Cell Lung Cancer.

A cycle consists of 3 weeks. During week 1, patients receive MGd, docetaxel, and cisplatin treatment followed by 2 weeks without treatment.

Eligible patients will receive 1 or 2 doses of MGd, depending on cohort, and a single dose of docetaxel and cisplatin at 75 mg/m² during the first week of each cycle. Additionally, tumor response will be evaluated at the end of even numbered cycles (2, 4, and 6). Patients may stay on the study a maximum of 6 cycles.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

≥ 18 years old
ECOG score of 0, 1, or 2
Histologically confirmed diagnosis of non-small cell lung cancer

Exclusion Criteria:

Laboratory values demonstrating inadequate function of the following:

Bone marrow
Kidneys
Liver

and

Peripheral neuropathy Grade 2 or higher
Greater than 2 prior chemotherapy regimens

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

36

Study ID:

NCT00102505

Recruitment Status:

Completed

Sponsor:

Pharmacyclics LLC.

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There is 1 Location for this study

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The University of Texas MD Anderson Cancer Center
Houston Texas, 77030, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

36

Study ID:

NCT00102505

Recruitment Status:

Completed

Sponsor:


Pharmacyclics LLC.

How clear is this clinincal trial information?

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