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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date March 2023
Source Goethe University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

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™

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Allopurinol

Rasburicase


Locations

Country Name City State
Germany University Hospital, Medical Dept. II Frankfurt

Sponsors (1)

Lead Sponsor Collaborator
Goethe University

Country where clinical trial is conducted

Germany, 

Outcome

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
See also
  Status Clinical Trial Phase
Completed NCT00199056 - German Multicenter Trial for Treatment of Newly Diagnosed Acute Lymphoblastic Leukemia in Adults (06/99) Phase 4
Completed NCT00198978 - German Multicenter Trial for Treatment of Elderly Patients With Newly Diagnosed Acute Lymphoblastic Leukemia Phase 4
Completed NCT00199095 - Treatment of Elderly Patients (>65 Years) With Acute Lymphoblastic Leukemia Phase 4
Completed NCT00199108 - Treatment of Acute Lymphoblastic Leukemia or Aggressive Lymphoma With Relapse in Central Nervous System With Depocyt Phase 2/Phase 3
Completed NCT00199004 - Trial for Treatment of Adult Patients With Standard Risk Acute Lymphoblastic Leukemia With Chemotherapy and Rituximab Phase 4
Completed NCT00198991 - German Multicenter Trial for Treatment of Newly Diagnosed Acute Lymphoblastic Leukemia in Adults (07/2003) Phase 4
Completed NCT00199069 - German Multicenter Trial for Treatment of Newly Diagnosed Acute Lymphoblastic Leukemia in Adults (05/93) Phase 4