NPCE News & Events

Consensus $98.9M. Reiterates FY26 gross margin between 81.5% and 82.5% and increases Adjusted EBITDA to ($8.5M) and ($9.5M) compared to previous guidance between ($9.0M) to ($10.0M).

Reports Q1 revenue $22.1M, consensus $21.7M. "First quarter results reflect continued execution against the strategic priorities we outlined earlier this year," said Joel Becker, Chief Executive Officer of NeuroPace. "We remain focused on driving disciplined growth in our core RNS business, advancing our product roadmap, and progressing toward potential indication expansion, all while strengthening the operational foundation of the Company. We continue to progress NAUTILUS through the regulatory review process and remain encouraged by the totality of the dataset supporting the IGE indication expansion."

NeuroPace announced a major milestone in its clinical evidence program with the publication of 3-year results from the RNS System Post-Approval Study, PAS, in Neurology, alongside the Company's recent presentation of 12- and 18-month data from its ongoing NAUTILUS trial at the 2026 American Academy of Neurology Annual Meeting. The published PAS results reinforce the RNS System's well-established value in drug-resistant focal epilepsy, while the NAUTILUS presentation highlights continued progress in expanding the reach of responsive neurostimulation into idiopathic generalized epilepsy. In addition, NeuroPace recently presented 12- and 18-month data from its ongoing NAUTILUS study evaluating the RNS System as an adjunctive therapy for the treatment of antiseizure medication-resistant idiopathic generalized epilepsy with generalized tonic-clonic seizures. 18-month results showed a 77% median reduction in GTC seizures compared with baseline, with rapid and sustained reductions over time.