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Spots Global Cancer Trial Database for Study of XL228 in Subjects With Chronic Myeloid Leukemia or Philadelphia-Chromosome-Positive Acute Lymphocytic Leukemia

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Trial Identification

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

Interventions

XL228

Study Description

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:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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