Lung Cancer Clinical Trial

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A Study of BMS-663513 in Combination With Chemoradiation in Subjects With Non Small Cell Lung Carcinoma (NSCLC)

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Summary

The purpose of this study is to determine the maximum tolerated dose and assess the safety and tolerability of escalating doses of BMS-663513 when given in combination with either radiotherapy alone or radiotherapy plus paclitaxel and carboplatin.

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Eligibility Criteria

Inclusion Criteria:

NSCLC who are eligible to receive a 6 week course of RT
Part 1 - not candidates for definitive RT
Part 2 - candidates for definitive RT

Exclusion Criteria:

Severe COPD, pulmonary infection or interstitial pneumonitis
Recent cellulitis
Autoimmune disease

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

35

Study ID:

NCT00461110

Recruitment Status:

Terminated

Sponsor:

Bristol-Myers Squibb

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There are 4 Locations for this study

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The Cancer Institute Of New Jersey
New Brunswick New Jersey, 08901, United States
Nyu Clinical Cancer Center
New York New York, 10016, United States
Thomas Jefferson Univ Hospital
Philadelphia Pennsylvania, 19107, United States
University Of Texas Southwestern Medical Center
Dallas Texas, 75390, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Phase:

Phase 1

Estimated Enrollment:

35

Study ID:

NCT00461110

Recruitment Status:

Terminated

Sponsor:


Bristol-Myers Squibb

How clear is this clinincal trial information?

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