Lung Cancer Clinical Trial

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Phase I Combination Ixabepilone + Cisplatin

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Summary

The purpose of this study is to determine the highest dose of ixabepilone that can be given safely with cisplatin without causing severe or life-threatening side effects and for some patients with non-small cell lung cancer, the effects (good or bad) on your cancer will also be studied

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Eligibility Criteria

Escalation Phase Subjects: Primary solid tumor not curable by local measures such as surgery, radiation

Inclusion Criteria:

Men and women age ≥ 18

Exclusion:

More than 2 prior chemotherapy containing regimens for metastatic disease
No prior exposure to cisplatin or ixabepilone

Expansion Phase Subjects: Advanced Non-small cell lung cancer

Inclusion Criteria:

Men and women age ≥ 18

Exclusion:

No prior chemotherapy-containing regimen for metastatic disease
No prior exposure to cisplatin or ixabepilone

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

30

Study ID:

NCT00832117

Recruitment Status:

Completed

Sponsor:

R-Pharm

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There are 7 Locations for this study

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Georgetown University Medical Center
Washington District of Columbia, 20007, United States
The Cancer Institute Of New Jersey
New Brunswick New Jersey, 08901, United States
Penn State Milton S. Hershey Medical Center
Hershey Pennsylvania, 17033, United States
Local Institution
Lucca , 55100, Italy
Local Institution
Meldola (Fc) , 47014, Italy
Local Institution
Rimini , 47900, Italy
Local Institution
Viterbo , 01100, Italy
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How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

30

Study ID:

NCT00832117

Recruitment Status:

Completed

Sponsor:


R-Pharm

How clear is this clinincal trial information?

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