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MediWound (MDWD) Q1 2025 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for MediWound Ltd

Q1 2025 earnings summary

17 Mar, 2026

Executive summary

  • Entered 2025 with strong execution across clinical, commercial, and operational priorities, maintaining momentum from 2024.

  • First quarter 2025 revenue was $4.0 million, with full-year revenue guidance maintained at $24 million.

  • Advanced SCRX/EscharEx value-based restudy for venous leg ulcers, with global trial enrollment progressing as planned and interim analysis expected mid-2026.

  • Expanded strategic collaborations, including Kerecis, bringing nearly all major wound care companies into clinical research programs.

  • NexoBrid adoption grew globally, with record U.S. sales and high demand in Japan and Europe, outpacing manufacturing capacity; manufacturing expansion is on track for full operational capacity by year-end 2025.

Financial highlights

  • Q1 2025 total revenue was $4 million, down from $5 million in Q1 2024, mainly due to lower BARDA-funded development services.

  • Gross profit was $0.7 million (19% margin), up from $0.6 million (12% margin) year-over-year.

  • R&D expenses rose to $2.9 million from $1.5 million, reflecting investment in SCRX trials.

  • Operating loss was $5.2 million, compared to $3.7 million in Q1 2024.

  • Net loss was $0.7 million ($0.07/share) versus $9.7 million ($1.05/share) last year, driven by non-cash financial income from warrant revaluation.

  • Adjusted EBITDA loss was $4 million, up from $2.9 million year-over-year.

  • Cash and equivalents were $38.7 million as of March 31, 2025, down from $43.6 million at year-end 2024.

Outlook and guidance

  • Revenue guidance for 2025 remains at $24 million, with $30–$33 million projected for 2026.

  • No anticipated material impact from BARDA or DoD funding delays; all programs are back on track.

  • SCRX/EscharEx value-based trial recruitment is on schedule, with interim data expected mid-2026; head-to-head Phase II study to start in H2 2025.

  • New manufacturing facility expected to be operational by end of 2025, with regulatory approvals and commercial availability anticipated in 2026.

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