Logotype for Sedana Medical

Sedana Medical (SEDANA) Q2 2026 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Sedana Medical

Q2 2026 earnings summary

20 Jul, 2026

Executive summary

  • Submitted New Drug Application (NDA) to the FDA in June 2026, advancing US market entry and marking a major milestone.

  • Group net sales were SEK 49.1 million in Q2 2026, flat year-over-year at constant exchange rates, with strong growth in all direct markets except Germany, which saw a 22% decline due to lower ICU patient volumes.

  • Profitability improved with group EBITDA at -SEK 1.9 million in Q2 2026 (margin -4%), ex-US EBITDA margin at 2%, and gross margin rising to 73%.

  • Cash position at quarter-end was SEK 52 million, with a new SEK 50 million credit facility secured for additional flexibility during the FDA review.

  • Early Access Program in the US expanded, with several hospitals treating patients and more onboarding.

Financial highlights

  • Q2 2026 net sales: SEK 49.1 million, down 1% year-over-year but flat at constant exchange rates; core business sales up 1% excluding contract manufacturing.

  • Gross profit increased to SEK 35.8 million, with gross margin improving to 73% from 70% last year.

  • Group EBITDA improved to -SEK 1.9 million from -SEK 4.1 million; ex-US EBITDA was positive at SEK 1 million.

  • Cash and cash equivalents at quarter-end were SEK 52 million, down from SEK 81 million at the start of the quarter, mainly due to US program investments.

  • Operating expenses were SEK 46 million in Q2 2026.

Outlook and guidance

  • On track to deliver full-year guidance: approaching EBITDA break-even at Group level and mid- to high-single-digit EBITDA margin ex-US.

  • Expecting cash burn and CapEx to decrease significantly following the NDA submission, with only potential increases if FDA review requires additional work.

  • US regulatory decision expected in August or September for file acceptance, with potential approval in 6–10 months depending on Priority Review.

  • Preparations underway for direct US launch, with significant market expansion potential upon FDA approval.

Partial view of Summaries dataset, powered by Quartr API
AI can get things wrong. Verify important information.
All investor relations material. One API.
Learn more