Adult Acute Lymphocytic Leukemia Clinical Trial
Official title:
Multicenter Trial for Treatment of Acute Lymphoblastic Leukemia in Adults (05/93)
NCT number | NCT00199069 |
Other study ID # | GMALL09 |
Secondary ID | |
Status | Completed |
Phase | Phase 4 |
First received | |
Last updated | |
Start date | April 1993 |
Est. completion date | May 2001 |
Verified date | March 2023 |
Source | Goethe University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The study evaluates the efficacy and tolerability of a risk- and subtype-adapted chemotherapy over one year, followed by randomized either intensified or conventional maintenance therapy. It includes a distinct protocol for the subgroup 'mature B-ALL',
Status | Completed |
Enrollment | 720 |
Est. completion date | May 2001 |
Est. primary completion date | January 1999 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 15 Years to 65 Years |
Eligibility | Inclusion Criteria: - Acute Lymphocytic Leukemia - Age 15 - 65 years Exclusion Criteria: - Serious secondary diseases which may compromise intensified chemotherapeutical treatment - Serious psychiatric diseases, which may compromise compliance with therapy - HIV-1 or HIV-2 Infection - Pretreatment > 2 weeks or chemotherapy other than Vincristine and Steroids - Patients without central diagnosis who cannot be allocated to a risk group |
Country | Name | City | State |
---|---|---|---|
Germany | University Hospital, Medical Dept. II | Frankfurt |
Lead Sponsor | Collaborator |
---|---|
Goethe University | Deutsche Krebshilfe e.V., Bonn (Germany) |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | remission rate, disease free survival, overall survival | |||
Secondary | death in induction, toxicity, time and dose compliance |
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