An Extension Study of the Safety and Anti-leukemic Effects of Imatinib Mesylate in Adult Patients With Ph + Leukemia
Interventional
Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
To enable patients to continue to have access to study treatment
December 31, 2011
No
Novartis Pharmaceuticals
Study Director
Novartis Pharmaceuticals
United States: Food and Drug Administration
CSTI571A0110E2
NCT00171223
August 2004
April 2013
Name | Location |
---|---|
University of Michigan | Ann Arbor, Michigan 48109-0624 |
Johns Hopkins Oncology Center | Baltimore, Maryland 21287 |
UCLA Medical Center | Los Angeles, California 90095-7059 |
Oregon Health & Sciences University | Portland, Oregon 97201 |
New York Presbyterian Hospital | New York, New York 10021 |
Wayne State University/Kamanos Cancer Center | Detroit, Michigan 48201 |
H. Lee Moffet Cancer Center & Research Institute/Univ of South Florida | Tampa, Florida 33612 |
Northwestern Univ meical School/Robert H. Lurie Comprehensive Cancer Center | Chicago, Illinois 60611 |
Dana Faber Cancer Institute | Boston, Massachusetts 02115 |
C/O V. Ward - Washington Univ. school of Medicine | St. Louis, Missouri 63110 |
MD Anderson Cancer Center, University of Texas | Houston, Texas 77030 |