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BioPorto (One-pager): "Forward" strategy reset and capital raise support 2027 roadmap

BioPorto
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Following BioPorto’s new “Forward” strategy and recent DKK 43 million capital raise, we have updated our one-pager on the company. The update reflects the revised financial ambitions, including cash flow positivity targeted for H2 2027, and a measured roadmap for commercial adoption of the NGAL test with partners.

The latest update also incorporates the extended FDA timeline for the adult NGAL test (submission expected in H1 2027) and improved funding visibility following the November 2025 private placement, which covers funding for 2026 and around two-thirds of BioPorto’s total capital needs through to profitability.

BioPorto remains a unique diagnostics case, combining a validated, FDA-cleared biomarker platform with a scalable partner model and a clear path toward commercialization in acute kidney injury (AKI) diagnostics.

On Wednesday, 19 November, BioPorto is expected to report its Q3 2025 results, and later the same day at 11:00, management will present the results and answer questions from the audience. Sign up and ask questions: https://www.inderes.dk/videos/bioporto-praesentation-af-q3-2025-resultater

Disclaimer: HC Andersen Capital receives payment from BioPorto for a DigitalIR/Corporate Visibility subscription agreement. / Philip Coombes 08:57 17/11/2025

BioPorto is a Danish in-vitro diagnostics company with headquarters in Copenhagen, Denmark. The company was founded in 2000. BioPorto has one marketed product, the NGAL test, for early diagnosis of acute kidney injury (AKI), which is commercially available in Europe, Canada, Asia, and Israel. It has received breakthrough designation from the FDA for AKI in the pediatric indication, for which it is currently conducting data analysis following the completion of enrollment of patients for its Phase 3 study which will lead to an expected application to FDA. Future plans include further FDA submission for adult indication as well as other markets.

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