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Brief Title: A Study of BMS-663513 Administered in Combination With Chemotherapy to Subjects With Advanced Solid Malignancies
Official Title: A Phase I, Multiple Ascending Dose Study of BMS-663513, an Agonistic Anti-CD137 Monoclonal Antibody, Administered in Combination With Chemotherapy to Subjects With Advanced Solid Malignancies
Study ID: NCT00351325
Brief Summary: The purpose of this study is to assess the safety and tolerability of multiple escalating doses of BMS-663513 when given in combination with paclitaxel and carboplatin.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University Of Pennsylvania Medical Center, Philadelphia, Pennsylvania, United States
Magee-Womens Hospital Of Upmc, Pittsburgh, Pennsylvania, United States
University Of Virginia, Charlottesville, Virginia, United States
University Of Washington, Seattle, Washington, United States
Local Institution, Toronto, Ontario, Canada
Name: Bristol-Myers Squibb
Affiliation: Bristol-Myers Squibb
Role: STUDY_DIRECTOR