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Clinical Trial Summary

To evaluate the efficacy and the safety of a front-line treatment combining CHOP regimen and rituximab in patients aged 60 to 80 years with previously untreated AIL.


Clinical Trial Description

This is a multicentric, open-label, non-randomized clinical study, evaluating the efficacy and the safety of a front-line treatment combining CHOP regimen and rituximab in patients aged 60 to 80 years with previously untreated AIL.

It is anticipated that 25 subjects will be enrolled over 2 years (from 2005 / 2007).Analysis performed every 5 patients (based on triangular test).

The duration of the treatment period is approximately 25 weeks and patients are followed until Death.

The total Duration of the study is expected to be 2.5 years. ;


Study Design


Related Conditions & MeSH terms

  • Lymphoma
  • Untreated T-cell Angioimmunoblastic Lymphoma

NCT number NCT00169156
Study type Interventional
Source Lymphoma Study Association
Contact
Status Completed
Phase Phase 2
Start date December 2005
Completion date November 2012