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Verici Dx (VRCI) investor relations material
Verici Dx H1 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.H1 2025 earnings summary7 Oct, 2025
Executive summary
Achieved Medicare coverage for Tutivia in April, enabling full commercial launch, revenue recognition, and rapid payment cycles.
Raised over £6.35m in July, extending cash runway into at least H2 2026 and supporting commercial scale-up.
Transitioned to commercial stage with two validated products: Tutivia and PTRA (Clarava), with licensing agreement in place for PTRA with Thermo Fisher.
Expanded commercial team, now up to four salespeople and additional clinical support, driving growth and onboarding 30 transplant centers (16% of US volume).
Maintained revenue targets for the year, with strong momentum and significant acceleration in testing volumes expected in Q4, Q1, and H2 2025.
Financial highlights
Revenue for the period was $1.9m: $1.16m from Tutivia testing and $0.75m from Thermo Fisher licensing.
EBITDA loss for the period was $2.8m.
Cash at end of June was $0.5m, increasing to $5.3m at end of September after fundraising.
Net cash outflow from operating activities was $3.5m.
Loss per share was $0.01 for H1 2025.
Outlook and guidance
Revenue target for 2025 remains at $3.2m for Tutivia, with significant volume acceleration expected in H2 2025 and beyond.
Growth expected from new center onboarding and expanded sales team, with Q4 and Q1 highlighted as key periods.
Focus remains on U.S. market; global expansion considered longer-term.
Funds in place to support growth and market expectations for full-year performance.
How will Tutivia penetrate non-Medicare market?
Quantify expected PTRA royalty/milestone revenue.
What is the commercialization plan for Protega?
Impact of commercial payer rates on avg. price
When will new centers significantly impact revenue?
Quantify CMS initiative's impact on testing demand
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Frequently asked questions
Verici Dx Plc is an immuno-diagnostics development company that specializes in the kidney transplantation market. The company's focus is on creating prognostic and diagnostic tests for kidney transplant patients, aiming to improve patient outcomes through personalized medical management. Verici Dx commercializes RNA signature-based tests that leverage artificial intelligence and transcriptomic analysis to provide insights into the immune response and other biological pathway signals crucial for the prognosis of risk of injury, rejection, and graft failure in transplant patients. These tests form a comprehensive kidney transplant platform designed for personalized patient and organ response risk assessment. Verici Dx's lead products include Tutivia, a post-transplant test aimed at detecting acute rejection, including sub-clinical rejection, and Clarava, a pre-transplant prognosis test for the risk of early acute rejection. The company is headquartered in Penarth, Wales and its shares are listed on the London Stock Exchange.
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