Last updated on December 2019

A Study Comparing Obinutuzumab and BGB-3111 Versus Obinutuzumab Alone in Treating R/R Follicular Lymphoma


Brief description of study

The purpose of the study is to evaluate the efficacy, safety and tolerability and of BGB-3111plus obinutuzumab versus obinutuzumab alone in subjects with relapsed/refractory non-Hodgkin follicular lymphoma.

Detailed Study Description

This is an open-label, randomized active control study of BGB-3111 plus obinutuzumab versus obinutuzumab alone in subjects with relapsed or refractory follicular lymphoma. Randomization is 2:1 and subjects will be stratified by the number of prior lines of therapy (2 - 3 vs > 3) and rituximab-refractory status. The study will evaluate the efficacy, as measured by overall response rate by independent review, safety and tolerability. Pharmacokinetic profile of BGB-3111 and obinutuzumab combination therapy will also be evaluated.

Clinical Study Identifier: NCT03332017

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Essey-lès-Nancy, France
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Goyang-si, Korea, Republic of
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Seoul, Korea, Republic of
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Seoul, Korea, Republic of
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Otahuhu, New Zealand
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Institut Catal d'Oncologia

L'Hospitalet De Llobregat, Spain
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London, United Kingdom
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Medway NHS Foundation Trust

Gillingham, United Kingdom
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Clinic Louis Pasteur

Essey-lès-Nancy, France
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Clinic Louis Pasteur

Essey-lès-Nancy, France
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