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BioPorto

1.07 DKK-0.93 %10.7. klo 17.59
Less than 1K followers

BIOPOR

NASDAQ Copenhagen

Biotechnology & Pharmaceuticals

Health Care

Overview
Financials & Estimates
Ownership
Dividend
Investor consensus
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-0.93 %
-10.88 %
+9.79 %
-0.84 %
+4.41 %
-23.93 %
-14.80 %
-64.45 %
-55.30 %

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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Market cap
527.29M DKK
Turnover
76.35K DKK
Revenue
EBIT %
P/E
Dividend yield-%
Coverage
Disclaimer
Michael Friis
Michael Friis

Head of Equities

Revenue and EBIT-%
EPS and dividend
Financial calendar
20.8.
2026

Interim report Q2'26

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Latest analysis report

Released: 22.05.2026

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Press release08.07.2026 klo 09.55

DNB Carnegie Access: BioPorto: Awaiting a decision on KDIGO – H1 preview

BioPorto
Regulatory press release16.06.2026 klo 00.02

Grant of Warrants

BioPorto
Press release09.06.2026 klo 19.30

DNB Carnegie Access: BioPorto: ProNephro validation study set to commence

BioPorto

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Regulatory press release09.06.2026 klo 13.28

BioPorto initiates U.S. Adult Validation Study following U.S. Food and Drug Administration (FDA) feedback

BioPorto
BioPorto (Investment Case): Q1 2026, advancement on the three pillars central to the long-term potential
Research22.05.2026 klo 15.30 by
Michael Friis, Victor Skriver

BioPorto (Investment Case): Q1 2026, advancement on the three pillars central to the long-term potential

In connection with the publication of BioPorto's Q1 2026 interim results, we have updated our investment case. Our investment case covers the key investment reasons, risks, and valuation perspectives.

BioPorto
Press release21.05.2026 klo 16.01

DNB Carnegie Access: BioPorto: KDIGO guidelines likely the next trigger – Q1 review

BioPorto
BioPorto – Præsentation af Q1 2026 resultater
Webcast21.05.2026 klo 12.00

BioPorto – Præsentation af Q1 2026 resultater

BioPorto offentliggør sin delårsrapport for Q1 2026 den 21. maj 2026. Samme dag kl. 11.00 vil CEO Carsten Buhl og CFO Klaus Juhl Wulff i et online event tage os igennem kvartalets resultater og den kommercielle udvikling, og du har mulighed for at stille spørgsmål.

BioPorto
Regulatory press release21.05.2026 klo 09.55

BioPorto announces Interim Result for the First Quarter of 2026

BioPorto
Regulatory press release24.04.2026 klo 17.22

Resolutions of the Annual General Meeting

BioPorto
Regulatory press release14.04.2026 klo 21.00

Grant of Warrants

BioPorto
Regulatory press release13.04.2026 klo 11.49

Major Shareholder Announcement

BioPorto
Press release09.04.2026 klo 18.50

DNB Carnegie Access: BioPorto: Time to walk the talk: stepping up with ProNephro - initiating coverage

BioPorto
Regulatory press release08.04.2026 klo 16.16

BioPorto Successfully Completes Divestment of its Antibody Business to Janel Life Sciences, LLC

BioPorto
BioPorto (Investment Case): Executing on the Forward strategy with adult pre-submission filed in Q1 2026
Research01.04.2026 klo 17.37 by
Michael Friis

BioPorto (Investment Case): Executing on the Forward strategy with adult pre-submission filed in Q1 2026

In connection with the publication of BioPorto's annual report for 2025 and recent announcements, we have updated our investment case. 2025 was a year of strategic repositioning for BioPorto. Revenue grew 11% to DKK 40.3m, driven by 25% growth in US NGAL RUO sales to DKK 18.4m and the first ProNephro AKI distributor revenues of DKK 4.3m via Roche. The gross margin improved to 75% from 68%, while adj. EBITDA loss widened to DKK -76.5m (from -70.6m) as R&D costs increased to DKK 50.5m, driven by the adult clinical study. BioPorto ended 2025 with 44 active US hospitals and DKK 54.9m in cash following two private placements totalling approximately DKK 77m.

BioPorto
Regulatory press release31.03.2026 klo 18.43

BioPorto Advances U.S. Adult Urine NGAL Program with FDA Pre-Submission Request After Positive EPACRA AKI Cut Off Analysis

BioPorto
Regulatory press release26.03.2026 klo 10.00

Notice convening the Annual General Meeting in BioPorto A/S

BioPorto
Regulatory press release26.03.2026 klo 08.43

BioPorto announces the Annual Report for 2025

BioPorto
Regulatory press release18.03.2026 klo 19.54

BioPorto Successfully Completes Preliminary Analysis of U.S. Adult NGAL Cutoff Study; Pre-Submission expected by End of Q1 2026

BioPorto
Regulatory press release09.02.2026 klo 09.11

BioPorto A/S Appoints Chief Financial Officer

BioPorto
BioPorto: Strong end to 2025, guidance points to continued momentum in 2026
Analyst Comment06.02.2026 klo 08.00 by
Michael Friis

BioPorto: Strong end to 2025, guidance points to continued momentum in 2026

BioPorto yesterday, after market close, delivered preliminary 2025 figures, set new 2026 guidance, confirmed the mid-term targets set out in the new "Forward" strategy, and updated on business development and expected regulatory timelines.

BioPorto