Verici Dx (VRCI) H1 2024 earnings summary
Event summary combining transcript, slides, and related documents.
H1 2024 earnings summary
9 Oct, 2026Executive summary
Shifted from research and product development toward commercial revenue across licensing, direct sales, and services.
Commercialized Clarava, licensed to Thermo Fisher, and Tutivia, sold directly; ProTeगा remains in development.
Expanded product applicability to other organs and adjacent diseases, using a research asset of physical samples and transcriptome data.
Advanced US market access and collaborations, including the Westmead Institute for Medical Research partnership.
Financial highlights
H1 2024 revenue was $3.339m, from Clarava licensing and urine-data services; FY 2023 revenue was $1.0m.
EBITDA loss was $1.1m; net loss was $1.348m.
Cash at 30 June 2024 was $7.015m, versus $2.6m at 31 December 2023; net cash increased by $4.264m.
Operating cash outflow was $3.177m for H1, down from $4.8m in H1 2023.
Outlook and guidance
Cash runway is expected to extend into 2026, based on assumptions for commercial rollout, Thermo Fisher milestones, licensing, services, and research collaborations.
Medicare Technical Assessment determination for Tutivia is expected by end-2024; retrospective reimbursement may be possible.
Protega 12-month visits are complete; data cleaning is underway, with analysis and initial validation data expected in H1 2025.
Remaining Thermo Fisher milestones are on track, subject to its launch plans; future royalties and milestone payments are anticipated.
Latest events from Verici Dx
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H1 2026 - 32% Q1 revenue growth and $3.7m in 2025 highlight strong US adoption and scale-up potential.VRCI
H2 2025 - Tutivia testing volumes surged 32% sequentially in Q1 2026, driving strong commercial momentum.VRCI
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H2 2025 TU - Medicare coverage, fundraising, and new centers drive commercial growth and revenue momentum.VRCI
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H2 2024