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Medivir (MVIR) Q1 2026 earnings summary

Event summary combining transcript, slides, and related documents.

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Q1 2026 earnings summary

5 May, 2026

Executive summary

  • Achieved a transformative quarter with strengthened financial position, including a SEK 45 million share issue, and significant progress in clinical programs for fostrox and MIV-711, with new rare disease opportunities and key studies advancing in Korea.

  • High engagement from hospitals and investigators in Korea for the FLEX-HCC liver cancer study, with four new hospitals added and two sites now open for patient enrollment.

  • Scientific Expert Council established for MIV-711 in Osteogenesis Imperfecta, advancing phase II proof-of-concept study preparations with strong external expert and patient organization engagement.

  • Vetbiolix's VBX-1000 (MIV-701) study in canine periodontitis has enrolled 22 of 51 dogs, with over 40% of subjects recruited and results expected in Q4 2026.

  • Management changes included the appointment of a new CFO and board restructuring.

Financial highlights

  • Net turnover for Q1 2026 was SEK 1.0 million, up from SEK 0.6 million in Q1 2025.

  • Operating loss for Q1 2026 was SEK -9.4 million, nearly SEK 4 million better than Q1 2025.

  • EBITDA loss improved to SEK -8.8 million from SEK -12.6 million year-over-year.

  • Cash flow from operating activities was SEK -13.0 million; cash balance at quarter-end was SEK 149.1 million.

  • Cash position strengthened by SEK 45 million directed share issue.

Outlook and guidance

  • FLEX-HCC Phase 2 study in liver cancer aims to enroll 80 patients over 12 months, with topline results anticipated in H2 2027, targeting a >$2.5bn annual market.

  • MIV-711 phase II proof-of-concept study in osteogenesis imperfecta to target adults with milder disease, aiming for rapid enrollment in Europe and potential rare pediatric disease designation.

  • Vetbiolix study results for MIV-701 in dogs expected in Q4 2026, with significant royalty revenue potential post-launch.

  • Existing cash resources considered sufficient to complete planned clinical studies.

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