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Sponsored by: |
Novartis |
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Information provided by: | Novartis |
ClinicalTrials.gov Identifier: | NCT00171223 |
This extension study will allow for further follow-up of the disease under treatment with imatinib mesylate and allow patients to continue to receive imatinib mesylate.
Condition | Intervention | Phase |
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Philadelphia Positive Chronic Myeloid Leukemia in Accelerated Phase, Acute Lymphoblastic Leukemia, Acute Myeloid Leukemia |
Drug: imatinib mesylate |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Non-Randomized, Open Label, Active Control, Single Group Assignment, Safety/Efficacy Study |
Official Title: | An Extension Study of the Safety and Anti-Leukemic Effects of Imatinib Mesylate in Adult Patients With Ph + Leukemia |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Inclusion Criteria
Exclusion Criteria
Other protocol-defined inclusion/exclusion criteria may apply.
Study ID Numbers: | CSTI571A0110E2 |
Study First Received: | September 12, 2005 |
Last Updated: | September 6, 2007 |
ClinicalTrials.gov Identifier: | NCT00171223 |
Health Authority: | United States: Food and Drug Administration |
Chronic Myelogenous Leukemia CML Philadelphia Chromosome Accelerated phase Acute Myelogenous Leukemia |
AML Acute Lymphoblastic Leukemia ALL Imatinib mesylate |
Philadelphia Chromosome Leukemia, Lymphoid Precursor Cell Lymphoblastic Leukemia-Lymphoma Immunoproliferative Disorders Chronic myelogenous leukemia Hematologic Diseases Acute myelogenous leukemia Myeloproliferative Disorders Leukemia, Myeloid |
Leukemia, Myeloid, Acute Imatinib Leukemia Lymphatic Diseases Leukemia, Myelogenous, Chronic, BCR-ABL Positive Lymphoproliferative Disorders Bone Marrow Diseases Acute myelocytic leukemia Lymphoma |
Neoplasms Neoplasms by Histologic Type Molecular Mechanisms of Pharmacological Action Immune System Diseases Antineoplastic Agents |
Therapeutic Uses Enzyme Inhibitors Protein Kinase Inhibitors Pharmacologic Actions |