Safety and Effectiveness of Blood-Brain Barrier Disruption (BBBD) in Subjects With Suspected Infiltrating Glioma

NCT ID: NCT04667715

Last Updated: 2025-05-02

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-10-23
• Study Completion Date: 2024-10-23

Brief Summary

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).

Detailed Description

After being informed about the study and potential risks, all patients giving written informed consent will undergo screening to determine eligibility for study entry. Patients who meet the eligibility requirements will be randomized in a 2:1 ratio to Exablate Test Arm and to Control Arm, respectively. The following assessments will occur:

1. Pre-surgical planning and Post-surgical visit MRI exams with and without contrast will be collected for evaluation by the study core lab; Any return to surgery for additional resection will be captured

2. All subjects will be seen at ~Week 2, and ~4-Weeks post resection for physical and neurological exams and to assess for complications or adverse events. These visits should coincide with standard (Neuro-oncology) care following resection.

3. Long-term outcomes will be collected during standard of care Neuro-oncology care follow-up visits for up to 2 years post resection; standard of care MRIs and RANO assessments will be collected.

Conditions

Glioma

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Exablate Test Arm

Subjects will undergo ExAblate BBBD prior to their standard of care tumor removal

Group Type: ACTIVE_COMPARATOR

Exablate BBBD

Intervention Type: DEVICE

Blood brain barrier disruption using ExAblate Type 2 device using microbubble resonators

Control Test Arm

Subjects will undergo their standard of care tumor removal

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

Exablate BBBD

Blood brain barrier disruption using ExAblate Type 2 device using microbubble resonators

Intervention Type: DEVICE

Eligibility Criteria

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

• Minimum Eligible Age: 21 Years
• Maximum Eligible Age: 85 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

InSightec

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Graeme Woodworth, MD

Role: PRINCIPAL_INVESTIGATOR

University of Maryland, Baltimore

Locations

University of Maryland

Baltimore, Maryland, United States

The University of Texas MD Anderson Cancer Center

Houston, Texas, United States

Countries

United States

Other Identifiers

BT011

Identifier Type: -

Identifier Source: org_study_id