drugset / Trial / NCT02232386

Phase 2 Study to Assess Activity & Safety of Front-line Ibrutinib + Rituximab in Unfit Chronic Lymphocytic Leukemia

NCT02232386 ↗

Phase 2 Completed 156 enrolled GIMEMA Foundation
NaSingle-groupOpen-labelTreatment

Summary

The present study aims at evaluating whether treatment with two different drugs, Ibrutinib and Rituximab is both efficient and safe for newly diagnosed patients with chronic lymphocytic leukemia.

Timeline

Start
2015-03-02
Primary completion
2018-04
Completion
2024-04-16

Drugs

EvaluationDrugModalityDoseRoute
Subject Ibrutinib Small molecule 420 mg Oral
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous