Investor Update
Logotype for Cyclopharm Limited

Cyclopharm (CYC) Investor Update summary

Event summary combining transcript, slides, and related documents.

Logotype for Cyclopharm Limited

Investor Update summary

26 Dec, 2025

Strategic growth and market expansion

  • Secured major US contracts, including a five-year VA agreement and the largest private healthcare network, validating product capabilities and driving momentum for 2025.

  • Technegas is now sold in 66 countries, with direct marketing in 17, leveraging a global sales and service footprint and over 5 million patient procedures performed.

  • US FDA approval and CMS reimbursement in 2024 enabled a commercial launch, with significant revenue growth and expansion initiatives beyond pulmonary embolism.

  • Targeting 2,000 of 8,000 US nuclear medicine departments, aiming for 250-300 installations by late 2026.

  • US market strategy focuses on generator placements with recurring consumable revenue, estimating $70,000 per site annually.

Financial performance and outlook

  • Achieved record sales revenue of $27.6 million, up 5% year-on-year, with Technegas revenue at $15.2 million and third-party distribution at $12.4 million.

  • US Technegas revenue reached $827,000 by December, with strong momentum and a 131% increase in H2 over H1.

  • Net loss after tax was $13.2 million, reflecting increased US investment and higher costs.

  • Closed 2024 with AUD 20.6 million in cash, supporting ongoing growth strategies.

  • Successful $20 million capital raising and $4 million share purchase plan in 2024 demonstrate strong shareholder support.

Product and technology leadership

  • Technegas is recognized as the agent of choice in nuclear medicine guidelines across 66 countries and endorsed by European and Canadian guidelines.

  • Over 5 million patient studies conducted; product delivers true functional ventilation imaging with low radiation and superior diagnostic accuracy.

  • FDA-approved for broad respiratory indications, enabling expansion beyond pulmonary embolism without further approvals.

  • Unique drug-device-service combination creates regulatory barriers and recurring revenue via per-patient consumables.

  • AI and analytical software integration are enhancing imaging capabilities and clinical value.

Partial view of Summaries dataset, powered by Quartr API
AI can get things wrong. Verify important information.
All investor relations material. One API.
Learn more