Lung Cancer Clinical Trial

A Study To Find The Best Dose Of SU011248 When Given With Pemetrexed, Pemetrexed And Cisplatin Or Pemetrexed And Carboplatin In Patients With Advanced Solid Tumors

Summary

This study will assess the maximum tolerated dose, overall safety and antitumor activity of SU011248 in combination with pemetrexed, pemetrexed and cisplatin or pemetrexed and carboplatin in patients with advanced solid tumors.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Patients with a diagnosis of a solid cancer which is not responsive to standard therapy or for which no standard therapy exists.
Patient has a good performance status (ECOG 0 or 1).

Exclusion Criteria:

Prior treatment with either pemetrexed or SU011248.
Coughing up blood within 4 weeks before starting study treatment (small amounts okay).
Hypertension that cannot be controlled by medications.

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

96

Study ID:

NCT00528619

Recruitment Status:

Completed

Sponsor:

Pfizer

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There are 3 Locations for this study

See Locations Near You

Pfizer Investigational Site
Aurora Colorado, 80045, United States
Pfizer Investigational Site
Ottawa Ontario, K1H 8, Canada
Pfizer Investigational Site
Montreal Quebec, H2L 4, Canada

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

96

Study ID:

NCT00528619

Recruitment Status:

Completed

Sponsor:


Pfizer

How clear is this clinincal trial information?

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