Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06222138

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

Led by Institut Claudius Regaud · Updated on 2026-02-13

80

Participants Needed

1

Research Sites

270 weeks

Total Duration

On this page

Sponsors

I

Institut Claudius Regaud

Lead Sponsor

N

NovoCure Ltd.

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older at the time of study entry
  • Newly diagnosed glioblastoma
  • Planned treatment with radio-chemotherapy followed by TTFields that has not yet started
  • Signed written informed consent
  • Able and willing to participate and comply with the study protocol
  • Affiliated with a Social Health Insurance in France
Not Eligible

You will not qualify if you...

  • Any condition preventing required sampling procedures
  • Contraindication to the medical device delivering TTFields
  • Simultaneous participation in another therapeutic interventional clinical trial
  • Pregnant or breastfeeding
  • Known positive test for hepatitis B, hepatitis C, HIV, or AIDS
  • Psychological, familial, geographic, or social issues preventing consent or compliance
  • Legal restrictions such as loss of freedom, legal protection, curatorship, or guardianship

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

IUCT-O

Toulouse, France

Actively Recruiting

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Research Team

E

Elizabeth COHEN-JONATHAN MOYAL

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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