12th Annual Cantor Fitzgerald Global Healthcare Conference
Logotype for NeuroPace Inc

NeuroPace (NPCE) 12th Annual Cantor Fitzgerald Global Healthcare Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for NeuroPace Inc

12th Annual Cantor Fitzgerald Global Healthcare Conference summary

9 Sep, 2026

Regulatory and clinical progress

  • Pursuing FDA approval for expanded indication into idiopathic generalized epilepsy (IGE), which could open up 20% more of the epilepsy market.

  • Currently engaged in the Submission Issue Request (SIR) process with the FDA after receiving a not approvable letter; meeting expected in early to mid Q4.

  • Breakthrough Device designation allows for collaborative FDA interactions; approval could occur as early as Q2 next year if a major amendment is required.

  • Clinical data shows 77% median seizure reduction at 18 months and 100% at 24 months for IGE patients.

  • Confident in existing data supporting broad IGE population, though limited representation in patients under 12 may require future amendments.

Core business performance and growth drivers

  • Core RNS business grew 21% in the most recent quarter, with strong prescriber and patient pipeline growth.

  • Adult focal epilepsy market remains under-penetrated; only a fraction of eligible patients receive intervention.

  • Investments in sales, marketing, and patient navigators aim to deepen utilization at comprehensive epilepsy centers and expand into community settings.

  • Clinical adoption is broadening as physicians become more comfortable with network stimulation and hybrid approaches.

  • Adoption dynamics for IGE are compelling due to easier procedures and potential for community-based treatment.

Data, AI, and digital initiatives

  • Over 27 million intracranial EEG recordings create a unique, longitudinal data set that serves as a competitive moat.

  • Recently launched ECoG Assistant (AI tool) to help physicians quickly identify relevant brainwave data, reducing analysis time by up to 10 minutes per patient.

  • Remote monitoring and programming capabilities are planned for FDA submission by year-end, aiming to reduce friction for patients outside major centers.

  • Data collaborations with pharmaceutical companies support drug trials and personalized treatment adjustments.

  • Monetization focus remains on device sales, with high ASP and gross margins over 80%; SaaS monetization not prioritized due to under-penetration.

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