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Study Of SU011248 In Combination With Docetaxel In Patients With Advanced Cancer

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Summary

This study is determining the maximum tolerated dose and safety of SU011248 (sunitinib malate, SUTENT) in combination with docetaxel (Taxotere). Several dosing regimens will be tested in patients with advanced solid tumors, including non small cell lung cancer.

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Eligibility Criteria

Inclusion Criteria:

Advanced solid tumor malignancy ECOG 0 or 1

Exclusion Criteria:

Prior treatment with with high-dose chemotherapy requiring stem cell rescue Prior irradiation to ≥25% of the bone marrow (e.g. whole pelvis=25%) Patients with centrally located lung lesions unless recently treated with radiotherapy

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

49

Study ID:

NCT00712504

Recruitment Status:

Completed

Sponsor:

Pfizer

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There are 4 Locations for this study

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Pfizer Investigational Site
Birmingham Alabama, 35233, United States
Pfizer Investigational Site
Birmingham Alabama, 35233, United States
Pfizer Investigational Site
Birmingham Alabama, 35294, United States
Pfizer Investigational Site
Nashville Tennessee, 37232, United States
Pfizer Investigational Site
Madison Wisconsin, 53792, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

49

Study ID:

NCT00712504

Recruitment Status:

Completed

Sponsor:


Pfizer

How clear is this clinincal trial information?

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