Clinical trial · Interventional
Safety and Effectiveness of Blood-Brain Barrier Disruption (BBBD) in Subjects With Suspected Infiltrating Glioma
A Pivotal Study to Evaluate the Safety and Effectiveness of Exablate Model 4000 Using Microbubble Resonators to Temporarily Mediate Blood-Brain Barrier Disruption (BBBD) in Subjects With Suspected Infiltrating Glioma
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Company decision to switch to other trials
Summary
Brief summary (as posted)
The purpose of this study is to evaluate the safety and effectiveness of using the Exablate Type 2 system using microbubble resonators (Exablate Test Arm) to disrupt the Blood-Brain Barrier for the purpose of temporarily transforming, and thereby 'marking', regions of infiltrating gliomas prior to planned surgical resection, for the purpose of improving tumor visualization during the surgery to achieve a greater proportion of subjects who receive a Gross Total Resection (GTR) per plan compared to those not undergoing a BBBD procedure prior to resection (Control Arm).
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Glioma | Glioma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Exablate BBBD | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- ACTIVE_COMPARATOR
- label
- Exablate Test Arm
- description
- Subjects will undergo ExAblate BBBD prior to their standard of care tumor removal
- interventionNames
- Device: Exablate BBBD
- type
- NO_INTERVENTION
- label
- Control Test Arm
- description
- Subjects will undergo their standard of care tumor removal
Primary outcomes (2)
- measure
- Overall safety of the Exablate BBBD procedure itself as measured through the collection of adverse events
- timeFrame
- Approximately 2 months
- description
- Safety of the Exablate BBBD procedure will be evaluated by patient examination and post-procedure MRI exams assessing changes in the treated region. Adverse events will be reported by the Investigator and monitored in both treatment arms.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 21 Years
- Maximum age
- 85 Years
Show eligibility criteria text
Inclusion Criteria: 1. Male or Female between 21-85 years of age who are able and willing to give informed consent 2. Subjects with suspected Grade II, III or IV infiltrating glioma (IG) on pre-operative brain imaging scans who have a non-enhancing component and are planned for surgical resection. 3. Karnofsky Performance Score 70-100 4. Able to communicate sensations during the Exablate BBBD procedure Exclusion Criteria: 1. Tumor originating from the deep midline, thalamus, midbrain, cerebellum or brainstem. 2. Multifocal tumors 3. MRI or clinical findings of: 1. Active or chronic infection(s) or inflammatory processes 2. Acute or chronic hemorrhages, specifically any lobar microbleeds, and no siderosis, amyloid angiopathy, or macro-hemorrhages 3. Intracranial thrombosis, vascular malformation, cerebral aneurysm or vasculitis 4. More than 30% of the skull area traversed by the sonication pathway is covered by scars, scalp disorders (e.g., eczema), or atrophy of the scalp 5. MR non-compatible metallic implants in the skull or the brain or the presence of unknown MR unsafe devices 6. Significant cardiac disease or unstable hemodynamic status 1. Documented myocardial infarction within six months of enrollment 2. Unstable angina on medication 3. Unstable or worsening congestive heart failure 4. Left ventricular ejection fraction below the lower limit of normal 5. History of a hemodynamically unstable cardiac arrhythmia 6. Cardiac pacemaker 7. Patient has right-to-left, bidirectional, or transient right-to-left cardiac shunts 8. Subjects with relative contraindications to perflutren including subjects with a family or personal history of QT prolongation or taking concomitant medications known to cause QTc prolongation, 9. Perflutren sensitivity or allergy ii. QT prolongation observed on screening ECG (QTc \> 450 for men and \>470 for women) 7. Uncontrolled hypertension (systolic \> 180 and diastolic BP \> 120 on medication) 8. Unable to discontinue use of anti-coagulant/antiplatelet therapy as per local standard. 9. History of a liver disease, bleeding disorder, coagulopathy or a history of spontaneous hemorrhage or evidence of increased risk of bleeding 10. Abnormal coagulation profile (Platelets \< 80,000), PT (\>14) or PTT (\>36), and INR \> 1.3. 11. Large lacunar lesions that cannot be navigated around 12. Known cerebral or systemic vasculopathy 13. Significant depression and at potential risk of suicide 14. Known sensitivity/allergy to gadolinium, or other intravascular contrast agents 15. Active seizures despite medication treatment (defined as \>1 seizure per week) which could be worsened by disruption of the blood brain barrier 16. History of anaphylactic shock 17. Active drug or alcohol disorder which have a higher risk for seizures, infection and/or poor executive functioning 18. Positive HIV status, which can lead to increased entry of HIV into the brain parenchyma leading to HIV encephalitis 19. Potential blood-borne infections which can lead to increased entry to brain parenchyma leading to meningitis or brain abscess 20. Any contraindications to MRI scanning, 21. Impaired renal function with estimated glomerular filtration rate \<30 mL/min/1.73m2 22. Severe Respiratory Illness 23. Currently in a clinical trial involving an investigational product or non-approved use of a drug or device 24. Pregnancy or Lactation
References
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