ClearPoint Neuro Inc. has announced encouraging results from a Phase I-II clinical study evaluating the ClearPoint Prism Neuro Laser Therapy System for the treatment of primary and recurrent glioblastoma and grade 4 astrocytoma. The study, conducted at Skåne University Hospital in Lund, Sweden, included fourteen patients and assessed the safety, feasibility, and efficacy of the device. Findings indicated improved survival compared to matched open surgery controls and demonstrated a safe, feasible, and reproducible workflow with a median ablation time of 6.5 minutes. No device-related events or complications were reported. The results from this study will be presented at the 75th Annual Congress of Neurological Surgeons $(CNS)$ in Los Angeles, scheduled for October 13-15, 2025.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. ClearPoint Neuro Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 1084118) on October 07, 2025, and is solely responsible for the information contained therein.
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