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Brief Title: Study of XL228 in Subjects With Chronic Myeloid Leukemia or Philadelphia-Chromosome-Positive Acute Lymphocytic Leukemia
Official Title: A Phase 1 Dose-Escalation Study of the Safety, Pharmacokinetics, and Pharmacodynamics of XL228 Administered Intravenously to Subjects With Chronic Myeloid Leukemia (CML) or Philadelphia-Chromosome-Positive Acute Lymphocytic Leukemia (Ph+ ALL)
Study ID: NCT00464113
Brief Summary: The purpose of this study is to determine the safest dose of the BCR-ABL inhibitor XL228, how often it should be taken, and how well people with leukemia tolerate XL228.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
UCLA School of Medicine, Los Angeles, California, United States
University of California San Francisco, San Francisco, California, United States
Georgetown University Medical Center, Lombardi Comprehensive Cancer Center, Washington, District of Columbia, United States
H. Lee Moffitt Cancer Center & Research Institute, Tampa, Florida, United States
University of Michigan Health System, Ann Arbor, Michigan, United States
MD Anderson Cancer Center, Houston, Texas, United States