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Enzyme Replacement Therapy
Exablate BBBD with Cerezyme for Parkinson's Disease
N/A
Waitlist Available
Research Sponsored by InSightec
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 3 months
Awards & highlights
Study Summary
This trial is testing a new way to deliver a drug to Parkinson's patients using focused ultrasound to open the blood-brain barrier.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, an average of 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 3 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Contrast enhancement on MR imaging
Secondary outcome measures
Safety --Adverse events
Other outcome measures
Exploratory effectiveness of Cerezyme delivery via MRgFUS BBB Opening
Exploratory effectiveness of Cerezyme treatment via MRgFUS BBB Opening
Trial Design
1Treatment groups
Experimental Treatment
Group I: Open label single armExperimental Treatment1 Intervention
Using Exablate Model 4000 Type-2 to temporarily disrupt the blood brain barrier to deliver Cerezyme in patients with Parkinson's Disease.
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Who is running the clinical trial?
InSightecLead Sponsor
88 Previous Clinical Trials
3,700 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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