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Study of Biologic Tumor and Plasma Biomarkers of Response to TTFields in Patients Treated for Newly Diagnosed Glioblastoma

Study acronym: EXOFIELDS
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Primary and study completion dates: May 2028 to Nov 2029v9
  2. Notable Primary and study completion dates: Oct 2027 to May 2028v8
  3. Minor Start date changed from estimate of Aug 2024 to Aug 27, 2024v7
  4. Notable Trial status: Not Yet Recruiting to Recruiting
    • Site details revised
    v6
  5. Notable Start date: Jun 2024 to Aug 2024v5
Show 3 earlier versionsHide 3 earlier versions
  1. Notable Start date: Apr 2024 to Jun 2024v4
  2. Minor Start date: Mar 2024 to Apr 2024v3
  3. Notable Start date: Jan 2024 to Mar 2024v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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This trial is a translational, open-label, monocentric prospective study of 80 patients aiming to study resistance mechanisms as well as biomarkers of resistance or sensitivity to TTFields. The study will be conducted on a population of patients with newly diagnosed glioblastoma treated with radio-chemotherapy followed by TTFields in the context of either routine care or a clinical trial. In this study, the Optune® system (battery operated device which delivers TTFields to the brain) will not be under investigation. For each included patient, blood samples will be collected during baseline visit (before initiation of radio-chemotherapy), then before initiation of TTFields and every 3 months during TTFields treatment. Additional blood samples will be scheduled at recurrence (if applicable). Moreover, tumor samples (formalin paraffin embedded (FFPE) tumor block and fresh samples) will be collected from surgery specimen on primary tumor by the sponsor for analysis. In case of recurrence, and if a second surgery is possible, tumor samples will also be collected. Tumor samples will be collected from biopsies taken in the course of routine practice and from surgical specimens collected during surgical procedure. No additional biopsies will be performed for the study. Patients will be followed-up for time to progression and overall survival for a maximum duration of 24 months from the TTFields initiation. MRI performed by patients during the course of the study will be collected by the sponsor for additional future research purposes.
Trial Details
NCT Number NCT06222138
Lead Sponsor Institut Claudius Regaud
Collaborators: NovoCure Ltd.
Conditions
(from sponsor)
Glioblastoma
Related terms Glioblastoma
Enrollment 80 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov