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| Sponsored by: |
OSI Pharmaceuticals |
|---|---|
| Information provided by: | OSI Pharmaceuticals |
| ClinicalTrials.gov Identifier: | NCT00073489 |
Purpose
The objectives of this study are to evaluate the safety and efficacy of OSI-461 in CLL patients.
| Condition | Intervention | Phase |
|---|---|---|
|
Chronic Lymphocytic Leukemia |
Drug: OSI-461 |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study |
| Official Title: | A Pilot Trial of OSI-461 in Patients With Chronic Lymphocytic Leukemia |
| Estimated Enrollment: | 23 |
| Study Start Date: | May 2001 |
| Estimated Study Completion Date: | December 2003 |
The primary objective of this study is to determine the activity of OSI-461 given twice daily orally in previously untreated CLL patients. The secondary objective is to evaluate the safety profile of OSI-461 in this patient population.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| United States, Arizona | |
| Arizona Hematology & Oncology Associates | |
| Phoenix, Arizona, United States, 85012 | |
| United States, Colorado | |
| Rocky Mountain Cancer Centers | |
| Aurora, Colorado, United States, 80012 | |
| United States, Florida | |
| Florida Oncology Associates | |
| Jacksonville, Florida, United States, 32207 | |
| Ocala Oncology Center | |
| Ocala, Florida, United States, 34474 | |
| United States, Iowa | |
| Iowa Oncology Associates | |
| Cedar Rapids, Iowa, United States, 52403 | |
| United States, Missouri | |
| Oncology/Hematology Associates of Kansas City | |
| Kansas City, Missouri, United States, 64111 | |
| United States, North Carolina | |
| Piedmont Hem Onc Assoc, P.A. | |
| Winston Salem, North Carolina, United States, 27103 | |
| United States, Ohio | |
| Dayton Oncology/Hematology Consultants | |
| Dayton, Ohio, United States, 45439 | |
| United States, Oregon | |
| Willamette Valley Cancer Center | |
| Eugene, Oregon, United States, 97401 | |
| United States, South Carolina | |
| Cancer Centers of the Carolinas | |
| Greenville, South Carolina, United States, 29615 | |
| United States, Texas | |
| Tyler Cancer Center | |
| Tyler, Texas, United States, 75702 | |
| Southwest Regional Cancer Center | |
| Austin, Texas, United States, 78705 | |
| Hematology Oncology Associates of South Texas | |
| San Antonio, Texas, United States, 78229 | |
| United States, Virginia | |
| Oncology & Hematology Associates of Southwest Virginia | |
| Roanoke, Virginia, United States, 24101 | |
| United States, Washington | |
| Cancer Care Northwest | |
| Spokane, Washington, United States, 99202 | |
More Information
| Study ID Numbers: | OSI-461-005 |
| Study First Received: | November 21, 2003 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00073489 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
chronic leukemia leukemia CLL |
|
Lymphatic Diseases Leukemia Chronic Lymphocytic Leukemia Leukemia, Lymphoid Immunoproliferative Disorders |
Leukemia, Lymphocytic, Chronic, B-Cell Leukemia, B-cell, Chronic Lymphoproliferative Disorders Leukemia, B-Cell |
|
Lymphatic Diseases Leukemia Neoplasms Leukemia, Lymphoid Immunoproliferative Disorders |
Neoplasms by Histologic Type Immune System Diseases Leukemia, Lymphocytic, Chronic, B-Cell Lymphoproliferative Disorders Leukemia, B-Cell |