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Brief Title: Study of XL228 Administered Intravenously to Subjects With Advanced Malignancies
Official Title: A Phase 1 Dose-Escalation Study of the Safety, Pharmacokinetics, and Pharmacodynamics of XL228 Administered Intravenously to Subjects With Advanced Malignancies
Study ID: NCT00526838
Brief Summary: The purpose of this study is to assess the safety and tolerability of the multi-targeted protein kinase inhibitor XL228 (active against IGF1R, Src, FGFR, and BCR-Abl) administered as a once- or twice-weekly 1-hour intravenous infusion in subjects with advanced malignancies.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
UCLA Jonsson Comprehensive Cancer Center, Los Angeles, California, United States
Winship Cancer Institute of Emory University, Atlanta, Georgia, United States
University of Michigan Health System, Ann Arbor, Michigan, United States
Duke University Medical Center, Durham, North Carolina, United States