Pulse Biosciences Inc. has announced a research collaboration with The University of Texas MD Anderson Cancer Center to explore the use of its proprietary nPulse™ Vybrance™ Percutaneous Electrode System for the treatment of thyroid cancers. The collaboration will focus on a clinical study led by Dr. Victoria Banuchi to assess the safety and effectiveness of the company's nanosecond Pulsed Field Ablation™ (nsPFA™) technology in treating papillary thyroid microcarcinoma. The FDA has approved the Investigational Device Exemption for this first-in-human feasibility trial, which is expected to begin in early 2026 and enroll 30 subjects across two sites. Ongoing preclinical studies are also being conducted to evaluate the technology's impact on anaplastic thyroid carcinoma.
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. Pulse Biosciences Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20251209940573) on December 09, 2025, and is solely responsible for the information contained therein.
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