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Fluorescence Detection of Adult Primary Central Nervous System Tumors With Tozuleristide and the Canvas System
Sponsor: John Yu
Summary
The purpose of this study is to examine the use of a single dose of tozuleristide (24 or 36 mg) and the Canvas imaging system during surgical resection of primary central nervous system (CNS) tumors: Primary gadolinium enhancing (high grade) CNS tumors, primary non-gadolinium enhancing CNS tumors, and primary vestibular schwannoma. The primary objectives of the study is to see how well tozuleristide and the Canvas imaging system during surgical resection will show fluorescence among primary enhancing/high grade CNS tumors; and among the tumors that demonstrate tozuleristide fluorescence, to estimate the true positive rate and true negative rate of fluorescence in tissue biopsies, as well as sensitivity and specificity of tozuleristide fluorescence for distinguishing tumor from non-tumoral tissue. The secondary objectives of the study include evaluating the safety of tozuleristide and the Canvas imaging system, and to determine if the presence of remaining fluorescence at the time of surgery corresponds to remaining tumor evident on post-operative MRI images, or if the absence of fluorescence corresponds to evidence of no gross residual tumor on post-operative magnetic resonance imaging (MRI).
Official title: A Phase 2 Study of Fluorescence Detection of Adult Primary Central Nervous System Tumors in Subjects Receiving Tozuleristide and Imaged With the Canvas System
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
50
Start Date
2021-09-30
Completion Date
2025-03-06
Last Updated
2026-07-10
Healthy Volunteers
No
Conditions
Interventions
tozuleristide
tozuleristide 24 or 36 mg administered intravenously 1-24 hours prior to surgery
Canvas imaging system
imaging device attached to surgical microscope
Surgical resection of tumor
Standard of care surgical resection of tumor
Locations (1)
Cedars-Sinai Medical Center
Los Angeles, California, United States