Last updated on November 2018

A Phase 3 clinical study for patients with follicular lymphoma

Brief description of study

This study will compare the safety and effectiveness of PF-05280586 versus rituximab-EU in patients with CD20-positive, low tumor burden follicular lymphoma. The primary hypothesis to be tested in this study is that the effectiveness of PF-05280586, as measured by the Overall Response Rate, is similar to that of rituximab-EU.

Clinical Study Identifier: NCT02213263

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National Hospital Organization Kyushu Medical Center
Fukuoka-shi, Japan

National Hospital Organization Kyushu Cancer Center
Fukuoka-Shi, Japan

Fukuoka Wajiro PET Diagnostic Imaging Clinic
Fukuoka, Japan

Recruitment Status: Closed

Brief Description Eligibility Contact Research Team

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