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Study identifier: NCT05871021 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Protective VEGF Inhibition for Isotoxic Dose Escalation in Glioblastoma

Condition: Glioblastoma  ·  Sponsor: University Hospital Tuebingen

PhasePhase 2
Planned participants146
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

Glioblastoma is the most aggressive brain tumor and often recurs locally despite intensive treatment. Standard chemoradiotherapy with 60 Gy may not be sufficient to control the tumor, and dose escalation seems to be warranted, but causes more toxicity. To address this, the multicentric PRIDE trial employs two cycles of bevacizumab to achieve dose escalation isotoxically. The goal is improved survival without significantly increasing side effects. The study uses a simultaneous integrated boost with a total dose of 75 Gy in 2.5 Gy per fraction.

This description comes directly from the study's public registry record.

Talk to the study team

Barbara Gehler, Dr. med.  ·  +49 7071 29 83420  ·  pride_tuebingen@med.uni-tuebingen.de

Always discuss trial participation with your own doctor first.

Locations (9)

Department of Radiation Oncology, University Hospital AugsburgAugsburg, GermanyRecruiting
Department of Radiation Oncology, University Hospital KölnCologne, GermanyRecruiting
Department of Radiation Oncology, University Hospital FrankfurtFrankfurt, GermanyRecruiting
Department of Radiation Oncology, University Hospital FreiburgFreiburg im Breisgau, GermanyRecruiting
Department of Radiation Oncology, University Hospital LeipzigLeipzig, GermanyRecruiting
Department of Radiation Oncology, Medical Faculty MannheimMannheim, GermanyRecruiting
Department of Radiation Oncology, University Hospital, LMU MunichMunich, GermanyRecruiting
Department of Neurology, University Hospital RegensburgRegensburg, GermanyRecruiting
Department of Radiation OncologyTübingen, GermanyRecruiting

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Source record: clinicaltrials.gov/study/NCT05871021