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Pulse Biosciences Achieves Enrollment Target in NANOPULSE-AF IDE Pivotal Clinical Study Evaluating nPulse™ Cardiac Catheter System for Atrial Fibrillation Treatment

Key Takeaway: Pulse Biosciences has successfully reached its enrollment target of 164 patients for the NANOPULSE-AF pivotal clinical study. This study evaluates the nPulse Cardiac Catheter System for treating atrial fibrillation. The positive response from the electrophysiology community highlights the potential of the novel nano-PFA technology.

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POSITIVE FACTORS

  • Enrollment target of 164 patients achieved successfully.
  • Significant investigator interest in the nPulse Cardiac Catheter System.
  • Study conducted across 15 clinical sites, indicating broad engagement.

Full Press Release Details

HAYWARD, Calif.--(BUSINESS WIRE)--Pulse Biosciences, Inc. (Nasdaq: PLSE), a company leveraging its novel and proprietary Nanosecond Pulsed Field Ablation™ (nano-PFA or nsPFA™) technology, today announced that its NANOPULSE-AF Study has reached its enrollment target of 164 evaluable patients across 15 clinical sites. "The compelling first-in-human dataset from the nPulse Cardiac Catheter System created significant investigator interest within the EP community across the United States," said Vive

Frequently Asked Questions

What is the NANOPULSE-AF study?

The NANOPULSE-AF study evaluates the nPulse Cardiac Catheter System for atrial fibrillation treatment.

How many patients were enrolled in the study?

The study successfully enrolled 164 evaluable patients.

How many clinical sites participated in the study?

The study involved 15 clinical sites across the United States.

What technology does Pulse Biosciences use?

Pulse Biosciences leverages its proprietary Nanosecond Pulsed Field Ablation technology.

Last updated: Oct 7, 2026