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Clinical Trial Summary

The purpose of this study is to explore the safety profile and establish a recommended dose (RD) for phase II of the antibody-cytokine fusion protein L19TNF plus standard TMZ chemoradiotherapy in patients with newly diagnosed glioblastoma. The study will be conducted in three consecutive parts: a dose finding part to determine the RD of L19TNF in combination with chemoradiotherapy, followed by a signal seeking part that investigates first signs of activity and then an activity evaluation part that studies the efficacy of L19TNF in combination with chemoradiotherapy against chemoradiotherapy alone.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04443010
Study type Interventional
Source Philogen S.p.A.
Contact Teresa Hemmerle, PhD
Phone +390577017816
Email regulatory@philogen.com
Status Recruiting
Phase Phase 1/Phase 2
Start date January 20, 2021
Completion date December 2026

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