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Clinical Trial

Feasibility Assessment of a Medical Device for Tumour Cell Retention and Radiotherapy Sensitization in Patients With Suspected High-grade Glioma.

NCT: NCT07725640 · NOT_YET_RECRUITING

NCT IDNCT07725640
StatusNOT_YET_RECRUITING
Start Date2026-10-30
Completion2028-10-30
SponsorBatea Oncology (INDUSTRY)
First posted
Last updated

Brief Summary

This is a prospective, multicenter, single-arm, pilot clinical investigation, aimed at evaluating the safety and preliminary efficacy of the GlioHook implant in patients with high-grade glioma undergoing surgical resection followed by standard of care (SoC) treatment. GlioHook is a sterile medical device designed to be implanted after tumour resection surgery in suspected high grade glioma patients, covering the entire surface of the tumour resection margins, decreasing infiltration and focalizing the disease, while improving the effects of radiotherapy. Once implanted, GlioHook exerts a dual mechanism that combines tumour cell focalization and radiosensitization.

Frequently Asked Questions

What is Feasibility Assessment of a Medical Device for Tumour Cell Retention and Radiotherapy Sensitization in Patients With Suspected High-grade Glioma.?

Feasibility Assessment of a Medical Device for Tumour Cell Retention and Radiotherapy Sensitization in Patients With Suspected High-grade Glioma. is a clinical trial registered under NCT07725640. Current status: NOT_YET_RECRUITING.

What is the status of NCT07725640?

The current status of NCT07725640 (Feasibility Assessment of a Medical Device for Tumour Cell Retention and Radiotherapy Sensitization in Patients With Suspected High-grade Glioma.) is: NOT_YET_RECRUITING.

When did Feasibility Assessment of a Medical Device for Tumour Cell Retention and Radiotherapy Sensitization in Patients With Suspected High-grade Glioma. start?

Feasibility Assessment of a Medical Device for Tumour Cell Retention and Radiotherapy Sensitization in Patients With Suspected High-grade Glioma. started on 2026-10-30.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.