drugset / Trial / NCT01902862

An Efficacy and Tolerability Study of Bortezomib in Combination With Rituximab Standard Therapy in Participants With Relapsed or Refractory Follicular Lymphoma

NCT01902862 ↗

Phase 2 Terminated 7 enrolled Janssen-Cilag GmbH
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy (effectiveness) and tolerability (how well a participant can stand a particular medicine or treatment; ability to be used) of bortezomib in combination with rituximab standard therapy (medicine or medical care given to a participant for a disease or condition) in participants with relapsed or refractory (not responding to treatment) follicular lymphoma (a cancer of the lymph nodes \[or tissues\] in follicle).

Timeline

Start
2006-02
Primary completion
2007-08
Completion
2007-08

Outcome

Outcome not reported

Stopped (Enrollment): “Recruitment too slow”

Drugs

EvaluationDrugModalityDoseRoute
Subject Bortezomib Small molecule 1.6 mg/m2 Intravenous
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous

Indications