Artrya (AYA) H2 2026 earnings summary
Event summary combining transcript, slides, and related documents.
H2 2026 earnings summary
19 Aug, 2026Executive summary
Transitioned to first full year of commercial operations, securing three U.S. foundation customers and generating initial U.S. commercial revenues.
Achieved FDA clearance for SalixⓇ Coronary Plaque module, expanding clinical and commercial opportunities.
Completed $80 million capital raise to fund U.S. commercialisation and operational scale-up.
Launched SAPPHIRE Study with six major U.S. health systems to build clinical evidence and accelerate adoption.
Strengthened U.S. commercial infrastructure and leadership team to support growth.
Financial highlights
Reported revenue remained flat at $28,000, with SaaS revenue (before non-cash adjustments) increasing to $177,000 from $28,000 year-over-year.
Operating loss increased 53.5% to $25.18 million (2025: $16.41 million), including $5.9 million in non-cash expenses related to partner affiliate options.
Cash balance at year-end was $44.0 million, with an additional $30.1 million in term deposits.
Net assets rose to $78.3 million from $21.3 million year-over-year.
No dividends declared or paid for the year.
Outlook and guidance
Focus for FY2027 is to deepen adoption within existing customers, expand to new health systems, and secure FDA clearance for SalixⓇ Coronary Flow.
Continued investment in product development, clinical evidence, and customer success to drive long-term growth.
SAPPHIRE Study expected to generate data for publication and support broader market adoption.
Latest events from Artrya
- 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 - First U.S. commercial revenues, strong cash, and SAPPHIRE study expansion drive growth.AYA
Q2 2026 TU - FDA clearance and new funding support imminent US and Australian expansion and product rollout.AYA
Q2 2025 TU - US regulatory progress, capital raise, and strategic growth with all resolutions approved.AYA
AGM 2024 - FDA clearance, $15m capital raise, and new contracts drive US and Australian expansion.AYA
Q3 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