Clinical Trials
LACOG 0213 - AUGMENT
Title
A phase 3, double-blind randomized study to compare the efficacy and safety of rituximab plus lenalidomide (CC-5013) versus rituximab plus placebo in subjucts with relapsed/refractory indolent lymphoma.
Primary Objective
To evaluate the efficacy (PFS) and safety of rituximab plus lenalidomide combination therapy in subjects with relapsed/refratory indolent lumphoma.
Design
This is a phase 3 multicenter, double-blind, randomized study is designed to evaluate the efficacy and safety of rituximab plus lenalidomide versus rituximab plus placebo.
Sample size: 350
Status: Follow up
LACOG Study Coordinator: Phillip Scheinberg
Sponsor: Celgene
Registry
Clinicaltrials.gov NCT01938001
Contact
lacog@lacog.org.br
Phone: 55 51 3384 5334