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Clinical Trial Summary

This study is a Phase 3 prospective, randomised, parallel-group, active controlled, double blind, multicentre, international study with 2 coprimary endpoints designed to demonstrate equivalence in pharmacokinetics (Part 1), as well as noninferiority in efficacy (Part 2), of CT-P10 to Rituxan when coadministered with CVP and to assess efficacy and safety in patients with advanced (stage III-IV) FL. Part 1 and Part 2 of the study will run in parallel.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02162771
Study type Interventional
Source Celltrion
Contact
Status Completed
Phase Phase 3
Start date July 14, 2014
Completion date December 29, 2018

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