Actively Recruiting
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
Eligibility Criteria
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
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
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
IUCT-O
Toulouse, France
Actively Recruiting
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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