CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 22 enrolled
Drug / intervention
Rituximab +2 moredrug
Likely dose
Rituximab 375 mg/m2from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00860457
NCT00860457Phase 2Completed

Lenalidomide Following Rituximab and Fludarabine in Untreated Chronic Lymphocytic Leukemia

Georgetown University·interventional·Posted Mar 12, 2009·Updated Nov 21, 2018

In Brief

A Phase 2 clinical trial evaluating Rituximab, Fludarabine, and 1 other intervention for Chronic Lymphocytic Leukemia. Completed, enrolled 22 participants across 1 site.

Detailed Summary

This study is for patients with chronic lymphocytic leukemia (CLL) who have not yet received any treatment for their disease. Current therapy for this disease includes the use of combination chemotherapy regimens containing Fludarabine and Rituximab, which have been found to be very effective for CLL. In this study, subjects will receive Fludarabine and Rituximab. After 3 cycles or 6 cycles of Fludarabine and Rituximab treatment, they will receive Lenalidomide. We are doing this research because we are attempting to improve the response, or outcome, of Fludarabine and Rituximab in previously untreated CLL patients. Lenalidomide is a drug that alters the immune system and it may also interfere with the development of tiny blood vessels that help support tumor growth. Therefore, in theory, it may reduce or prevent the growth of cancer cells. Lenalidomide is approved by the Food and Drug Administration (FDA) for treatment of specific types of myelodysplastic syndrome (MDS) and in combination with dexamethasone for patients with multiple myeloma (MM). MDS and MM are blood disorders that involve different types of blood cells. It is not approved for chronic lymphocytic leukemia. It is currently being tested in a variety of cancer conditions. In this case it is considered experimental. This research is being done because we are attempting to find a better treatment for chronic lymphocytic leukemia. We do not know the effect of Lenalidomide following the regimen of Fludarabine and Rituximab. The hypothesis of the study is that adding Lenalidomide after the standard treatment regimen of Fludarabine and Rituximab will have better outcomes than treatment with Fludarabine and Rituximab alone.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
CollaboratorsCelgene Corporation

Timeline

Phase 2CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedMar 12, 2009
Enrollment StartFeb 1, 2008
Primary CompletionMar 1, 2011
Study CompletionFeb 1, 2012
TodayJul 2, 2026
Enrollment to primary: 3.1 yearsPosted 17.3 years ago

Interventions

Rituximabdrug

375 mg/m2 IV infusion Day 1 of each 28-day cycle for maximum of 6 cycles

Fludarabinedrug

25 mg/m2 IV Days 1-5 of each 28-day cycle for maximum of 6 cycles

Lenalidomidedrug

5-10 mg PO daily on Days 1-21 of each 28-day cycle for a maximum of 6 cycles