Artrya (AYA) AGM 2026 summary
Event summary combining transcript, slides, and related documents.
AGM 2026 summary
13 Nov, 2026Opening remarks and agenda
AGM held in person in West Perth with a live Zoom broadcast; voting was limited to in-person ballots and proxies, with questions accepted from the floor and in advance.
Formal business covered seven resolutions; the proposed constitutional change was withdrawn and is planned to return at a future general meeting.
Financial performance review
Cash of $67.2m and nil debt as at 30 September 2026; FY26 R&D rebate of $4.8m due.
First U.S. revenue came from Salix Coronary Anatomy subscriptions and per-scan Salix Coronary Plaque fees; five commercial health systems had signed agreements, spanning 41 hospitals.
HonorHealth’s agreement includes an AUD 0.5m platform subscription plus per-scan fees for plaque and, after clearance, flow; plaque scan volumes rose across the quarters to September 2026.
The U.S. CCTA scan market was cited at US$4.4bn annually; CMS announced 2027 rates of US$395 for CCTA, US$950 for plaque assessment and US$850 for flow assessment.
Board and executive committee updates
Jeff Le Benger and Helen Kurincic joined the board and stood for election at the AGM; Clayton Hatch commenced as CFO in September, bringing U.S. healthcare commercialization experience.
A Chief People Officer and U.S. operations general manager were appointed; recruitment continued for experienced U.S. healthcare staff and a CTO.
Latest events from Artrya
- Huntsville deal and rising plaque use advance U.S. rollout; Flow filing delayed.AYA
Q1 2027 - Huntsville validates the SAPPHIRE sales pathway, with plaque and flow offering upside beyond AUD 500,000.AYA
Status update - Operating loss widened to $25.18m as U.S. commercialisation accelerated, supported by $80m capital raise.AYA
H2 2026 - Revenue rose to $5.46M, but net loss increased to $16.41M amid U.S. commercial expansion.AYA
H2 2025 - Net loss widened to $14.0m as US commercialisation advanced and cash reserves declined.AYA
H2 2024 - First U.S. revenues, FDA clearance, and A$80m capital raise mark a pivotal commercial shift.AYA
H1 2026 - FDA clearance and new funding support imminent US and Australian expansion and product rollout.AYA
Q2 2025 TU - FDA clearance enables rapid U.S. commercialization and AI-based coronary assessment.AYA
FDA Announcement - FDA clears real-time AI plaque module, enabling $950 reimbursement and rapid U.S. rollout.AYA
FDA Announcement