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XVIVO Perfusion (XVIVO) investor relations material
XVIVO Perfusion Q2 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Q2 2025 net sales were SEK 178 million, down 15% year-over-year, with organic growth at -11% and a weak US dollar further impacting results.
Strong growth in US lung sales to clinics (+26%), European liver sales (+32%), and US kidney sales (+47%), while Thoracic and Services segments declined.
Clinical trial results for heart and liver products showed strong efficacy and cost-effectiveness, supporting future commercialization.
Strategic investments in field force, R&D, and inventory are driving growth in targeted segments and supporting future demand.
Regulatory milestones achieved, including FDA approvals for key clinical studies and progress in Europe and Canada.
Financial highlights
Q2 net sales: SEK 178 million (down from SEK 210 million in Q2 2024); H1 net sales flat at SEK 396 million.
Gross margin stable at 74% in Q2 and H1; adjusted EBITDA margin at 13% for Q2, 18% for H1.
Q2 operating income (EBIT): SEK 7 million (down from SEK 33 million); H1 EBIT: SEK 34 million.
SEK 9 million positive operating cash flow in Q2; cash position at SEK 323 million at period end.
Investments totaled SEK 72 million in Q2, mainly for US clinical trials, R&D, and inventory.
Outlook and guidance
Cost restructuring prioritizes investments in field force and customer-facing roles to drive growth.
Heart product launches prepared for Europe, Australia/NZ, and Canada, pending regulatory approvals.
US regulatory and clinical activities for heart and liver ongoing; first US liver trial patient targeted for H2 2025.
Main growth drivers expected to be EVLP in the US and liver/kidney in Europe, with additional growth from heart post-approval.
Long-term outlook remains positive, with demand for transplants far exceeding supply and machine perfusion expected to drive future growth.
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