Adult Acute Lymphocytic Leukemia Clinical Trial
Official title:
Randomised Phase III Trial of Effectivity and Safety of Rasburicase Compared With Allopurinol for Treatment of Hyperuricemia in Patients With Acute Lymphoblastic Leukemia or High-Grade NHL With High Risk of Tumorlysis Syndrome (> 15 Yrs)
NCT number | NCT00199043 |
Other study ID # | GMALL08 |
Secondary ID | |
Status | Completed |
Phase | Phase 3 |
First received | |
Last updated | |
Start date | May 2003 |
Est. completion date | May 2008 |
Verified date | March 2023 |
Source | Goethe University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
In this study the efficacy and tolerability of two approaches to treat and prevent hyperuricemia is tested in patients with acute lymphoblastic leukemia or high-grade lymphoma with high risk of tumor lysis syndrome. Both arms are compared by randomisation. In one arm patients receive during pre-phase chemotherapy conventional prophylaxis with allopurinol whereas in the other arm Rasburicase is used.
Status | Completed |
Enrollment | 80 |
Est. completion date | May 2008 |
Est. primary completion date | May 2008 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 15 Years and older |
Eligibility | Inclusion Criteria: - patients of the GMALL B-ALL/NHL-Study 2002 - patients of the GMALL-Study 07/2003 - patients of the GMALL-Study Elderly 1/2003 which fulfill the following criteria: - bulky disease (> 7.5 cm) - high LDH (> 2 x UNL) - uric acid >8 mg/dl/ >475µmol/L at diagnosis - leukocytes > 30 000/µl Exclusion Criteria: - exclusion Criteria of the GMALL B-ALL/NHL Study 2002 or the GMALL-Study 07/2003 or GMALL-Elderly 1/2003 and: - asthma or severe, live-threatening atopic allergy in history - hypersensitivity against Uric acid - Glucose-6-Phosphate-Dehydrogenase deficiency - pretreatment with Rasburicase or Urikozyme™ |
Country | Name | City | State |
---|---|---|---|
Germany | University Hospital, Medical Dept. II | Frankfurt |
Lead Sponsor | Collaborator |
---|---|
Goethe University |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | renal function, uric acid, electrolytes, adverse events and mortality in pre-phase and the two following cycles of chemotherapy, time and dose compliance of chemotherapy | after cycle 1 | 3 weeks | |
Secondary | response rate, incidence of tumor lysis syndrome | after cycle 1 | 3 weeks |
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