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Clinical Trial Summary

An open-label study to determine the efficacy and safety of Rasburicase used for the prevention and treatment of tumor lysis syndrome


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00651911
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 4
Start date July 2003
Completion date July 2004

See also
  Status Clinical Trial Phase
Completed NCT01724528 - Febuxostat for Tumor Lysis Syndrome Prevention in Hematologic Malignancies Phase 3
Completed NCT00186940 - Rasburicase Treatment for Chemotherapy or Malignancy-Induced Hyperuricemia in Asthma/Allergy Patients N/A
Completed NCT00230217 - Study of Rasburicase as Treatment or Prevention of Hyperuricemia Associated With Tumor Lysis Syndrome in Patients With Relapsed or Refractory Lymphoma, Leukemia, or Solid Tumor Malignancy Phase 4
Completed NCT00360438 - Pharmacokinetic Evaluation of Rasburicase in Patients With Leukemia and/or Lymphoma at High Risk of TLS Phase 1/Phase 2
Completed NCT00628628 - Rasburicase in Patients at Risk for Tumor Lysis Syndrome Phase 2
Terminated NCT03605212 - Febuxostat for Tumor Lysis Syndrome Prevention in Hematological Malignancies of Paediatric Patients and Adults Phase 1/Phase 2
Terminated NCT01097369 - Elitek (Rasburicase) Immuno-Monitoring Study N/A
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