drugset / Trial / NCT01542918

Lenalidomide Plus Rituximab for Recurrent/Refractory CNS and Intraocular Lymphoma

NCT01542918 ↗

NaSingle-groupOpen-labelTreatment

Summary

This is a Phase I study, which means that the goal is to see if the study treatment is safe. The purpose of this study is to test the safety of Lenalidomide at different dose levels, and to test the safety of Lenalidomide alone or in combination with Rituximab (also known as Rituxan®).

Timeline

Start
2012-12-17
Primary completion
2016-04-07
Completion
2016-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 10 mg Oral
Subject Lenalidomide Other / unclassified 15 mg Oral
Subject Lenalidomide Other / unclassified 20 mg Oral
Subject Rituximab Monoclonal antibody 25 mg Intravenous
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous

Indications