Study of S-3304 in Patients With Locally Advanced Non-Small Cell Lung Cancer



Status:Completed
Conditions:Lung Cancer, Lung Cancer, Cancer, Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - 85
Updated:5/4/2018
Start Date:February 2003
End Date:October 26, 2006

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A Phase I/II Study of the Safety, Pharmacokinetic Interaction and Efficacy of S-3304 in Combination With Standard Therapy in Patients With Locally Advanced Non-small Cell Lung Cancer.

A study to measure the safety and effectiveness of S-3304 when given in combination with
conventional chemo-radiation therapy in patients with locally advanced non-small cell lung
cancer.

A two part study to evaluate the safety and efficacy of S-3304 in combination with standard
therapy in patients with locally advanced non-small cell lung cancer. The first part of the
study is a Phase I design to evaluate the maximum tolerated dose of S-3304 when given in
combination with radiation and paclitaxel/carboplatin chemotherapy that is appropriate for
further evaluation. The second part of the study is a randomized Phase II design to evaluate
the efficacy of recommended S-3304 dose in combination with chemo-radiation.

INCLUSION CRITERIA

- newly diagnosed non-small cell lung cancer of stage IIIA non-resectable or of stage
IIIB without pleural effusion

- ECOG performance status 0-1

- adequate organ function

- clinically indicated and able to receive conventional chemoradiation therapy

EXCLUSION CRITERIA

- patients with prior history of cancer, other than basal cell carcinoma after
appropriate treatment, or prior systemic chemotherapy treatment

- patients with other serious intercurrent illness including HIV/AIDS, or
contraindicated for paclitaxel/carboplatin or thoracic irradiation treatment
We found this trial at
5
sites
9500 Euclid Avenue
Cleveland, Ohio 44106
216.444.2200
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Kansas City, Kansas 66160
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La Jolla, California 92037
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Washington, District of Columbia 20007
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