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CellaVision (CEVI) investor relations material
CellaVision Q3 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Net sales declined by 1.7%–2% to SEK 176 million, with organic sales up 2.6% year-over-year despite a -4.3% FX headwind and mixed regional performance.
EBITDA rose to SEK 50 million, margin improved to 28%, and gross margin increased to 69%, reflecting operational efficiency.
Strategic progress included completion of a clinical trial and CE mark submission for the bone marrow application, with approval expected in early 2026.
Major software upgrade completed and validated, with rollout planned for the current quarter.
Cash flow from operating activities was SEK 29.6–30 million, impacted by working capital changes.
Financial highlights
Gross margin increased to 69%, up 1 percentage point year-over-year, aided by price increases and favorable product mix.
EBITDA for Q3: SEK 50 million (up from SEK 49 million); EBITDA margin: 28%.
Operating expenses totaled SEK 82 million, with reductions in sales/admin and increased R&D investment.
R&D investment was 24% of sales, with SEK 14 million capitalized, lower than usual due to vacation and software completion.
Cash and cash equivalents at quarter-end: SEK 159 million.
Outlook and guidance
CE mark for bone marrow application expected early 2026, with commercial launch activities planned for Q1 2026.
Software upgrade is expected to drive growth by enhancing product differentiation, with no additional fee for customers.
Continued R&D investment is planned, with possible changes in capitalization as projects mature or complete.
Management remains confident in long-term growth and value creation across all regions despite quarterly fluctuations.
U.S. reagent market entry expected mid-2026, with methanol-free stain as a key enabler.
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