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NCT03779230CompletedPhase 1/2

A study to evaluate the safety and efficacy of the tumor-targeting human antibody-cytokine fusion protein L19TNF plus lomustine in patients with glioblastoma at first progression

Source: EU CTIS (euclinicaltrials.eu) · Last updated 22 Dec 2025

Status (registry)
Completed
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
113 (actual)
First submitted
10 Oct 2022
Start date
31 Jul 2023
Lead sponsor
Philogen S.p.A.
Diseases
Glioblastoma
NCT number
NCT03779230
EU CT number
2022-501822-39-00

What you commit to

  • Study type: Interventional · Phase 1/2
  • Participants enrolled: 113
  • 12 sites in 3 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Sites (12)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Universitaetsklinikum Bonn AöR
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BonnGermanyCompleted
University Hospital Cologne AöR
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CologneGermanyCompleted
Klinikum rechts der Isar der TU Muenchen AöR
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MunichGermanyCompleted
Universitaetsklinikum Tuebingen
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TuebingenGermanyCompleted
Hospital Pierre Wertheimer
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BronFranceCompleted
Hopital Saint Louis
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ParisFranceCompleted
Hopital Universitaire Pitie Salpetriere
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Paris Cedex 13FranceCompleted
Instituto Di Ricovero E Cura A Catattere Scientifico
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BolognaItalyCompleted
The Foundation Of The Carlo Besta Neurological Institute IRCCS
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MilanItalyCompleted
Veneto Institute of Oncology
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PadovaItalyCompleted
Azienda Ospedaliera Universitaria Senese
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SienaItalyCompleted
Azienda Ospedaliero Universitaria Citta Della Salute E Della Scienza Di Torino
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TurinItalyCompleted

This page is information, not medical advice. Discuss any trial with your doctor.