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NCT Number: NCT05565443

MR-guided Focused Ultrasound Plus GCase

The goal of this study is to establish safety and feasibility of intracerebral delivery of GCase via MRgFUS. This technique may offer potential benefits given the exposure of the putamen to GCase in animal models has been shown to be efficacious in improving Parkinson's disease pathology and phenotype.

Recruiting

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Key information

Age range

35 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Sunybrook Research Institute

Toronto, Ontario, Canada

Location status: Recruiting

Location contact

Inthuja Suthananthan

CONTACT

[email protected]

647-687-8062

Nir Lipsman, M.D., Neurosurgery

PRINCIPAL_INVESTIGATOR

About this study

This is a two-arm, open-label, intervention only phase I/II clinical study. One arm of the study will enroll seven (7) GBA PD patients and the other arm seven (7) idiopathic PD patients. During the intervention phase, the first four subjects of each arm will receive three transcranial bilateral putamenal GCase at 30 IU/kg IV every two weeks, followed by 60 IU/kg in the next three subjects. Following three treatments in this study, the subjects will be followed for twelve months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Men or women between age 35 and 80 years, inclusive.
  • Able and willing to give informed consent.
  • Diagnosis of PD satisfying MDS Clinical Diagnostic Criteria for PD
  • At least 2 years from initial diagnosis
  • Hoehn and Yahr Stage 1-3 on PD medication
  • Dopaminergic deficit by a positive DAT SPECT scan
  • On stable regimen of PD medications for at least 90 days prior to the study
  • American Society of Anesthesiologists (ASA) score 1-3
  • Harbor at least one GBA mutation if enrolled in the GBA PD arm or two wild-type GBA alleles if enrolled in the idiopathic PD arm

Exclusion criteria

  • Positive pregnancy test (for pre-menopausal women).
  • Contraindication to DEFINITY ultrasound contrast agent or perflutren (e.g. hypersensitivity, known left or bidirectional cardiac shunt)
  • Contraindication to MRI or gadolinium-DTPA (e.g. incompatible device, hypersensitivity)
  • Insulin-dependent diabetes mellitus that is not well-controlled or that in the Investigator's opinion precludes participation in the study.
  • Severely impaired renal function with estimated glomerular filtration rate <30 mL/min/1.73m2 and/or on dialysis.
  • Currently participating in another clinical therapeutic trial
  • Patient receiving bevacizumab (Avastin) therapy
  • Subjects with evidence of cranial or systemic infection.
  • Cerebral or systemic vasculopathy.
  • Documented cerebral infarction within the past 12 months or TIA in the past 1 month.
  • Contraindication to GCase enzyme therapy, specifically previous hypersensitivity reaction to GCase enzyme therapy
  • Parkinsonism plus symptoms, secondary parkinsonism
  • Previous neurosurgical procedure for PD

Treatment and study plan

Blood Brain Barrier Disruption - Functional

Device

Delivery of GCase across the BBB to form a disease modifying strategy for patients with Parkinson's Disease

Primary outcomes

  1. Adverse Events

    Time frame: 12 Months

    Measure of the adverse events through the intervention phase and follow-up. All adverse events and/or Serious Adverse Events will be documented and reported according to CTCAE criteria.

Secondary outcomes

  1. Feasibility of MRgFUS BBB opening for GCase brain delivery

    Time frame: 12 Months

    Using MRI images to measure:

    • The qualitative measure of the MRI T1-weighted with gadolinium of contract extravasation in the sonicate putamen.
    • The qualitative measure of the dynamic contrast enhanced (DCE) MRI

Study contacts

Contact information is provided by the study sponsor or research team.

Alyssa Voelker-Christy

CONTACT

[email protected]

+1-817-948-5219

Sponsors and collaborators

Lead sponsor

InSightec

Industry

Registry information

Official study title

A Phase I/II Study for Bilateral Putamenal Delivery of Recombinant Glucocerebrosidase in Patients With Parkinson's Disease Using MR-guided Focused Ultrasound Induced Opening of the Blood-brain Barrier

Important dates

Study start
2022
Primary completion
2027
Study completion
2028
First posted
Oct 4, 2022
Registry last updated
Jan 23, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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