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Clinical Trial Summary

The purpose of this clinical trial is to prove the efficacy of the following new regimen treatment:

- Administration of anti-CD20 (Rituximab) combined with chemotherapy.

- Combined treatment with high doses of methotrexate and high doses of cytarabine with conventional cytostatics (block C)

- Prophylactic administration of G-CSF after all chemotherapy cycles

- local irradiation after 6 cycle if CNS was affected or if there are residual tumour


Clinical Trial Description

Clinical Trial with a pharmaceutical speciality in new conditions to use. ;


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 NCT00388193
Study type Interventional
Source PETHEMA Foundation
Contact
Status Completed
Phase Phase 2
Start date August 2006
Completion date December 2013

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