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Clinical Evaluation of Nelarabine (506U78)in Japanese Patients With Leukemia or Lymphoma
This study has been completed.
Study NCT00406757   Information provided by GlaxoSmithKline

First Received on November 30, 2006.   Last Updated on May 31, 2012   History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Lymphoblastic Lymphoma
Acute Lymphoblastic Leukemia
Additional conditions recognized in this trial
Leukemia
Leukemia, Lymphoid
Lymphoma
Lymphoma, Non-Hodgkin
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
More general conditions related to this trial
Immune System Diseases
Immunoproliferative Disorders
Lymphatic Diseases
Lymphoproliferative Disorders
Neoplasms
Neoplasms by Histologic Type
Interventions listed in this trial
Nelarabine injection 400mg/m2
Nelarabine injection 650mg/m2
Nelarabine injection 1000mg/m2
Nelarabine injection 1500mg/m2
Sponsors listed in this trial
GlaxoSmithKline


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