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CLL Tumor assessment FCR vs FC BO17072 NCT00090051 - Tumor assessment of Chronic Lymphocytic Leukemia NCT00090051 BO17072

- 10/28/15 - 1 form, 10 itemgroups, 45 items, 1 language
Itemgroups: Tumor assessment at screening, Indicator lesions, Non-indicator lesions, Liver and spleen examination, Tumor assessment after Cycle 3 and 6, Indicator lesions , Non-indicator lesions , Liver and spleen examination after Cycle 3 and 6, Response assessment after Cycle 3, Response assessment after Cycle 6
An open-label, multicenter, randomized, comparative, phase III study to evaluate the efficacy and safety of rituximab plus fludarabine and cyclophosphamide (FCR) versus fludarabine and cyclophosphamide alone (FC) in previously treated patients with CD20 positive B-cell chronic lymphocytic leukemia (CLL). FCR Versus FC Alone in the Treatment of Chronic Lymphocytic Leukemia (CLL) in Relapsed Patients NCT00090051 Roche BO17072

CLL Follow-Up Month 9 BO17072 NCT00090051 - Follow-Up Month 9 Chronic Lymphocytic Leukemia NCT00090051 BO17072

- 10/28/15 - 1 form, 8 itemgroups, 29 items, 1 language
Itemgroups: Bone marrow examination, Result of Bone marrow examination, Is bone marrow involved with CLL?, Tumor assessment, Indicator lesions, Non-indicator lesions, Liver and spleen examination, Response assessment
An open-label, multicenter, randomized, comparative, phase III study to evaluate the efficacy and safety of rituximab plus fludarabine and cyclophosphamide (FCR) versus fludarabine and cyclophosphamide alone (FC) in previously treated patients with CD20 positive B-cell chronic lymphocytic leukemia (CLL). NCT00090051 BO17072

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