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Clinical Trial Summary

Primary Objective:

To determine the incidence, titer and type of anti-rasburicase antibodies in the context of hypersensitivity reaction(s) or the loss of uricolytic activity occurring in patients with relapsed leukemia/lymphoma who have been re-treated with rasburicase and have experienced a hypersensitivity reaction or loss of uricolytic activity.


Clinical Trial Description

n/a


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01097369
Study type Observational
Source Sanofi
Contact
Status Terminated
Phase N/A
Start date February 2010
Completion date February 2010

See also
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Terminated NCT03605212 - Febuxostat for Tumor Lysis Syndrome Prevention in Hematological Malignancies of Paediatric Patients and Adults Phase 1/Phase 2
Active, not recruiting NCT04745910 - Pegloticase for the Reduction of Uric Acid in Patients With Tumor Lysis Syndrome Phase 4
Completed NCT00230178 - Rasburicase Versus Allopurinol in Tumor Patients at Risk for Hyperuricemia and Tumor Lysis Syndrome Phase 3