drugset / Trial / NCT01625741

Phase II Study of High-Dose Rituximab in High-Risk Chronic Lymphocytic Leukemia Patients in Suboptimal Response After Induction Immunochemotherapy

NCT01625741 ↗

NaSingle-groupOpen-labelTreatment

Summary

This study explores the potential to improve the quality of response obtained after induction treatment in Chronic Lymphocytic Leukemia (CLL), by giving a short and intense consolidation schema using high-dose rituximab. Patients in suboptimal response (Minimal Residual Disease persistence) after induction will be selected, as well as those who have a Minimal Residual Disease (MRD) relapse after having achieved MRD negativity.

Timeline

Start
2012-07
Primary completion
2015-05
Completion
2015-05

Outcome

Outcome not reported

Stopped: “Stopped by Principal Investigator decision”

Drugs

EvaluationDrugModalityDoseRoute
Subject Rituximab Monoclonal antibody 2000 mg Intravenous