Trial Information
Multicenter Trial for Treatment of Acute Lymphocytic Leukemia in Adults (Pilot Study 06/99)
Inclusion Criteria:
- Acute lymphoblastic leukemia (pro-B, common, pre-B, early T, T)
- Age 15-65 yrs (*55-65 years if biologically younger according to general condition)
Exclusion Criteria:
- Severe comorbidity
- Cytostatic pre-treatment
- Pregnancy
- Missing written informed consent
Type of Study:
Interventional
Study Design:
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Outcome Measure:
Remission rate,Remission duration,Disease free survival,Overall survival
Principal Investigator
Dieter Hoelzer, MD,PhD
Investigator Role:
Study Chair
Investigator Affiliation:
University Hospital Frankfurt, Medical Dept. II
Authority:
Germany: Federal Institute for Drugs and Medical Devices
Study ID:
GMALL10
NCT ID:
NCT00199056
Start Date:
October 1999
Completion Date:
Related Keywords:
- Adult Acute Lymphocytic Leukemia
- ALL
- Treatment
- De Novo
- Adult
- Leukemia
- Leukemia, Lymphoid
- Precursor Cell Lymphoblastic Leukemia-Lymphoma