drugset / Trial / NCT01625741
Phase II Study of High-Dose Rituximab in High-Risk Chronic Lymphocytic Leukemia Patients in Suboptimal Response After Induction Immunochemotherapy
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Rituximab | Monoclonal antibody | 2000 mg | Intravenous |