Q1 2025  
Interim Report  
BioPorto Group  
May 8, 2025  
nnnnnnnnnnnnnnnnnnn  
BioPorto A/S  
Tuborg Havnevej 15, ground floor
DK-2900 Hellerup
CVR DK-17500317
 
Consolidated Financial Highlights  
2025 2024 2024  
Jan 1 Mar 31  
Jan 1 Mar 31  
Jan 1 - Dec 31  
DKK million (except where noted)  
Revenue  
(Unaudited)  
(Unaudited)  
7.7  
4.9  
9.5  
7.2  
36.2  
24.5  
Gross profit  
Sales and marketing costs  
Research and development costs  
Administrative costs  
Loss before financial items (EBIT)  
Financial items, net  
Loss before tax  
Net loss  
Comprehensive loss  
Adjusted EBITDA  
8.1  
17.7  
9.9  
(30.8)  
(0.4)  
(31.2)  
(27.5)  
(26.8)  
(28.1)  
6.0  
6.3  
9.6  
(14.7)  
(0.2)  
(14.9)  
(13.6)  
(13.7)  
(15.3)  
30.2  
33.5  
36.2  
(75.5)  
1.7  
(73.7)  
(68.2)  
(69.5)  
(70.6)  
Non-current assets  
Cash and cash equivalents  
Current assets  
Total assets  
Equity  
Non-current liabilities  
Current liabilities  
Total equity and liabilities  
15.8  
32.8  
58.9  
74.7  
41.4  
6.9  
7.4  
45.3  
64.1  
71.4  
41.7  
3.9  
12.1  
59.7  
83.9  
96.0  
67.8  
7.8  
26.4  
74.7  
25.8  
71.4  
20.4  
96.0  
Cash flows from operating activities  
Cash flows from investing activities  
Of which investment in property, plant, and  
equipment  
Cash flows from financing activities  
Net cash flows  
(24.1)  
(1.8)  
(20.7)  
0.3  
(83.6)  
1.2  
(1.4)  
(1.0)  
(26.9)  
-
(0.9)  
(21.3)  
(0.4)  
75.5  
(6.9)  
Revenue growth  
Gross profit percentage  
-19%  
64%  
18%  
76%  
17%  
68%  
Equity ratio (solvency)  
55%  
58%  
71%  
Average number of employees  
Number of shares at the end of the period (1,000)  
Loss per share (EPS), DKK  
Net asset value per share, period-end, DKK  
Share price, period-end, DKK  
48  
27  
38  
429,670  
(0.06)  
0.10  
379,670  
(0.04)  
0.11  
429,670  
(0.17)  
0.16  
1.38  
1.31  
1.55  
Note: Loss per share (EPS) is calculated in accordance with IAS 33 “Earning per share”. Other financial ratios have been calculated in accordance with the  
guidelines from the Danish Society of Financial Analysts and 2024 BioPorto Annual Report.  
Reconciliation of Adjusted EBITDA  
Loss before financial items (EBIT)  
Depreciation and amortization  
Share-based compensation expenses  
Severance costs  
(30.8)  
0.7  
0.4  
(14.7)  
0.6  
(4.8)  
3.6  
(75.5)  
2.4  
(0.9)  
3.4  
1.6  
Adjusted EBITDA  
(28.1)  
(15.3)  
(70.6)  
Interim Report BioPorto, first three months of 2025  
2
 
Non-IFRS Financial Measure  
In the Interim Report, BioPorto discloses a financial measure of the Group’s financial performance that reflects adjustments to the most directly comparable  
measures calculated and presented in accordance with IFRS. This non-IFRS financial measure may not be defined and calculated by other companies in the  
same manner and may thus not be comparable.  
The non-IFRS financial measure presented in the Interim Report is Adjusted earnings before interest, taxes, depreciation, and amortization (Adjusted  
EBITDA).  
Adjusted EBITDA is an alternative measure of performance utilized by management, investors, and investment analysts to evaluate and analyze the  
Company’s results. Adjusted EBITDA excludes non-cash share-based compensation and non-recurring costs (e.g., restructuring charges, merger and  
acquisition integration costs), if any. We believe that earnings exclusive of non-cash and non-recurring costs is a key indication of how a company is  
progressing from period to period and that the non-IFRS financial measure Adjusted EBITDA is useful to investors, lenders, and other creditors because  
such information enables them to better understand earnings exclusive of non-cash and non-recurring costs from period to period. However, we also  
believe that Adjusted EBITDA data has limitations, particularly as non-cash and non-recurring costs could significantly impact our performance. We  
therefore limit our use of Adjusted EBITDA and do not evaluate our results and performance without considering both non-IFRS Adjusted EBITDA on the  
one hand and net income or loss on the other. We caution the readers of this report to follow a similar approach by considering data on Adjusted EBITDA  
only in addition to, and not as a substitute for or superior to, net income or loss in accordance with IFRS.  
Interim Report BioPorto, first three months of 2025  
3
 
Management Review  
The enrollment of patients during the first three months of 2025 has been  
progressing at a faster pace than initially expected, demonstrating strong  
engagement and efficiency in the process. As a result, we are on track to  
achieve our 2025 milestones, including the enrolment of the first patient in  
the validation study scheduled for Q3 2025.  
Total revenue in line with expectations and guidance for  
2025 maintained  
Revenue for the first three months of 2025 was lower than the same period  
last year, which was in line with expectations. Revenue totaled DKK 7.7  
million, a 19% decrease compared to Q1 2024, due to a shift in timing of  
bulk NGAL orders for the rest of the world from Q1 2025 to later in 2025.  
NGAL tests sales in the U.S. continued to increase and were up 20%  
compared to Q1 2024. However, total NGAL sales decreased by 25%  
compared to the same period last year, due to lower NGAL test sales in the  
rest of the world (ROW). For the coming quarters we expect to see  
increasing sales, especially for ROW.  
The cut-off study is the first of two studies which will form a substantial part  
of the adult submission for US clearance of ProNephro AKI (NGAL),  
scheduled to be submitted to FDA by 2026. The enrollment of patients  
follows the successful process path implemented by BioPorto’s regulatory  
team leveraging the experience from the US pediatric clearance process,  
which was successfully concluded with a US marketing clearance in  
December 2023.  
Revenue from sales of antibodies saw a decline of 6% compared to the  
same period last year. Sales of ELISA kits, representing 7% of total revenues,  
decreased 21% compared to the same period last year.  
BioPorto expects the FDA submission could lead to a clearance for clinical  
use in adult patients by 2027, allowing the test to be commercially  
distributed in the US and hence opening up a large part of what is estimated  
to be a USD 3 billion yearly market for the test worldwide.  
The revenue for the first quarter aligns with our expectations, and we  
maintain our full-year 2025 guidance of DKK 45-60 million.  
Ongoing funding considerations  
Strengthening of commercial activities and organization  
On April 15, 2025, BioPorto completed a fully subscribed funding round of  
25,000,000 new shares at market price providing gross proceeds of DKK  
33.5 million. The proceeds are to be applied to finance clinical trials to seek  
FDA clearance for ProNephro AKI(NGAL) for adult use in the United  
States, increase sales and marketing activities as well as general corporate  
purposes until the beginning 2026. Going forward, we will investigate  
alternative financing options to optimize shareholder value  
The primary focus in the first quarter of 2025, has been on the preparation  
of the US commercial launch of ProNephro AKI TM (NGAL) for pediatric and  
young adults, and rest of the world (ROW).  
In the first quarter of 2025, we optimized our leadership structure to  
enhance operational effectiveness. This builds on the commercial platform  
improvements made during 2024, when we strengthened our commercial  
structure in the US by adding sales and medical liaison roles to intensify  
efforts to drive demand. BioPorto participated in and hosted several  
presentations in both the US and Europe during the first quarter of 2025  
and maintained a high attendance at conferences. The activities and the  
strengthening of the commercial setup has led to increased awareness,  
which continues to generate new customers.  
Global Partnerships on Distribution of NGAL Tests  
An important element in BioPorto’s commercialization plan is to secure  
strategic partnerships with the “Big 5” clinical instrument vendors to drive  
instrument expansion that are FDA cleared for ProNephro AKI (NGAL).  
We remain dedicated to progressing the commercial launch of the  
ProNephro AKI (NGAL) in the US on Roche Cobas® c501 analyzer which is  
expected in the second quarter of 2025.  
Expanding the global distribution network with the leading instrument  
manufacturers and driving expansion of instruments cleared for ProNephro  
AKI (NGAL) and the NGAL Test use will enable more laboratories to  
implement the test and increase the serviceable market fast and prepare  
for a forceful roll-out of the test for adults once expectedly cleared in the  
US by 2027.  
Preparation of FDA application for ProNephro AKI (NGAL)  
for adults  
Late 2024, BioPorto enrolled the first patient in its US clinical study for  
ProNephro AKI (NGAL) with the goal of determining a cut-off point for risk  
stratification of moderate to severe of AKI in adult patients.  
Interim Report BioPorto, first three months of 2025  
4
 
Financial Review  
This financial review is based on the Group’s consolidated financial  
information as of and for the three months ended March 31, 2025, with  
comparative results as of and for the three months ended March 31, 2024,  
in brackets.  
of business development and sales force to commercialize ProNephro AKI  
(NGAL) in the US and grow NGAL revenue in the rest of the world (ROW).  
Research and Development Costs  
Research and development costs, consisting of research and development,  
regulatory affairs, quality assurance, clinical, and medical affairs, totaled in  
the first quarter of 2025 DKK 17.7 million (DKK 6.3 million), with the  
increase mainly due to our adult clinical study of DKK 10.1 million.  
Revenue  
Revenue was DKK 7.7 million (DKK 9.5 million) in the first three months of  
2025.  
NGAL test sales totaled DKK 4.6 million (DKK 6.1 million) in the first three  
months of 2025, which comprised 60% of total revenue. NGAL revenue in  
the US/Canada totaled DKK 4.5 million (DKK 3.7 million) in the first three  
months of 2025, which comprised 58% of total revenue. Antibody sales  
totaled DKK 2.5 million (DKK 2.7 million) in the first three months of 2025.  
Administrative Costs  
Administrative costs in the first quarter of 2025 totaled DKK 9.9 million (DKK  
9.6 million). The increase in costs is due to carry-over of additional staff  
being hired in the second half of 2024; offset by the severance costs that  
incurred in the first quarter of 2024.  
Figure 1. Revenue by quarter (DKK million)  
12  
Financials Items, net  
9.7  
8.6  
9.5  
Financial income and expenses reflect interest income/expense and  
currency transaction gains/losses. Financial items, net for the first quarter  
of 2025 were an expense of DKK 0.4 million (DKK 0.2 million)  
9.2  
7.8  
10  
8
8
7.8  
6.6  
7.7  
6
4
Tax Benefit  
2
In the first quarter of 2025, a DKK 3.8 million tax benefit (DKK 1.3 million)  
was recognized. The tax benefit is primarily related to tax credits held by its  
Danish entities associated with the Company’s investment in research and  
development.  
0
Q1  
Q2  
2023  
Q3  
2025  
Q4  
2024  
EBIT/Adjusted EBITDA  
For the first quarter of 2025, Earnings before interest and taxes (EBIT) was  
a loss of DKK 30.8 million (DKK 14.7 million), and adjusted EBITDA was a loss  
of DKK 28.1 million (DKK 15.3 million), reflecting the mix of variances  
described above.  
Figure 2. NGAL test product revenue by quarter (DKK  
million)  
8
6.8  
5.8  
7
6
5
4
3
2
1
0
6.1  
5.4  
Cash and Cash equivalents  
4.8  
4.8  
4.6  
4.6  
As of March 31, 2025, BioPorto’s cash position was DKK 32.8 million (DKK  
45.3 million) and is deposited at major, national Danish, Nordic, and US  
banks. The Company continually evaluates its liquidity requirements,  
capital needs and availability of capital resources based on its operating  
needs and planned initiatives. The Company’s assessment as to the  
adequacy of liquidity relies inter alia on assumptions and significant  
judgements (in addition to those matters discussed cf. Note 2). These  
assumptions are applied in the Companys budgets and forecasts as well as  
customary sensitivities, existing capital resources and assumptions  
concerning the timing, costs and resources required to undertake the  
Company’s strategic priorities and tactical decisions. This includes the US  
clinical commercial launch of ProNephro AKI (NGAL) for pediatric and young  
adults, commercialization activities for NGAL tests under CE Mark and  
Antibodies in Europe, supply chain management, and ongoing R&D, all of  
which under current circumstances remain difficult to predict.  
3.4  
Q1  
Q2  
Q3  
Q4  
2023  
2024  
2025  
Gross Profit  
Gross profit for the first quarter of 2025 was DKK 4.9 million (DKK 7.2  
million), the decrease was driven by lower revenue and lower margin due  
to higher consultancy costs and staff costs compared to prior year period.  
The Company assessed its liquidity and capital resources based on sufficient  
cash in a fallback scenario should no additional financing be added in the  
next four quarters and concluded that these are adequate to fund  
operations considering a twelve-month period from the balance sheet date  
due to the Company’s ability to scale back its strategic initiatives based on  
Sales and Marketing Costs  
Sales and marketing costs totaled DKK 8.1 million (DKK 6.0 million) in the  
first quarter of 2025. The increase in sales and marketing costs was  
primarily driven by the carry-over from end of 2024 of staffing up in areas  
Interim Report BioPorto, first three months of 2025  
5
 
facts and circumstances. BioPorto has in the first three months of 2025  
continuously exercised strong cost control to preserve cash.  
Guidance for 2025 maintained  
For the first quarter of 2025, we are aligned with expectations and BioPorto  
therefore maintains its financial guidance for 2025, as most recently  
described in its Annual Report 2024 of:  
Net working capital  
Net working capital (i.e., current assets minus current liabilities) as of  
March 31, 2025, totaled DKK 32.5 million (DKK 38.3 million).  
Total Revenue target of DKK 45-60 million, and  
Adjusted EBITDA loss in the range DKK 75-85 million.  
In 2025, BioPorto expects revenue to grow 24-66% compared to 2024.  
Growth will be driven by increased sales of NGAL products primarily in  
the US following the FDA clearance, supplemented by growth in the rest of  
the world. NGAL sales in 2025 is expected to be back-end loaded.  
Cash Flow Statement  
Cash used in operating activities during the first three months of 2025  
totaled DKK 24.1 million (DKK 20.7 million), which reflected costs for the  
adult clinical study and the reasons described above.  
The expected adjusted EBITDA loss for 2025 will reflect higher marketing  
costs for ProNephro AKI (NGAL) in the US, and the cost of new clinical trials  
to support FDA clearance for ProNephro AKI (NGAL) for adults.  
Cash used in investing activities was DKK 1.8 million (inflow of DKK 0.3  
million). Cash used in financing activities was DKK 1.0 (DKK 0.9 million).  
The net cash flow during the first three months of 2025 was a use of DKK  
26.9 million (DKK 21.3 million).  
Forward-looking safe harbor statements  
This interim report contains forward-looking statements that involve risks,  
uncertainties, and other factors, many of which are outside of BioPorto’s  
control, that could cause actual results to differ materially from the results  
or expectations discussed in the forward-looking statements. Forward-  
looking statements include statements concerning the Group’s plans,  
objectives, goals, future events, performance and/or other information  
that is not historical information. All such forward-looking statements are  
expressly qualified by these cautionary statements and any other  
cautionary statements which may accompany the forward-looking  
statements. BioPorto does not undertake any obligation to update or revise  
forward-looking statements to reflect subsequent events or circumstances  
after the date made.  
Subsequent event  
Please see Note 13 for further details.  
Significant risks and uncertainties  
BioPorto faces a number of risks and uncertainties, including those  
common for the biotech/medical device industry and could potentially  
impact the Company across the value chain including clinical and  
regulatory, research and development, manufacturing, commercial, and  
financial activities. Furthermore, the uncertainty in the US could impact the  
company adversely by implementation of tariffs or delaying any  
submissions with the FDA.  
For Further Information  
Hanne Søgaard Foss, Head of Investor Relations, BioPorto, +45 4529 0000,  
investor@bioporto.com  
A variety of factors and events, including geopolitical uncertainty, have  
resulted in delays and other challenges in global supply chains. To  
manufacture its products, the Company is dependent on the supply of raw  
materials and key components from suppliers, some of which are single  
source suppliers. Delays in the manufacture, delivery, or quality of these  
components, or delays in the Company’s execution of its commercialization  
strategy, including hiring personnel and continuing to prepare  
manufacturing and quality systems, could affect the Company’s ability to  
deliver products to its customers, which could cause the Company’s results,  
prospects, and financial performance to be negatively impacted.  
www.bioporto.com  
In addition, a full description of risks can be found in BioPorto’s 2024 Annual  
Report in the section captioned “Risk Management”, which factors could  
materially affect the Group’s business, financial condition, and/or future  
results. The risks described in those sections and in this report are not the  
only risks BioPorto faces. Additional risks and uncertainties not currently  
known to management or the Group or that the Group currently deems to  
be immaterial may also have a material adverse effect on the Group’s  
business, future opportunities, financial condition, and/or operating  
results.  
Interim Report BioPorto, first three months of 2025  
6
 
Statement by the Board of Directors and  
Management  
The Board of Directors and Executive Management today reviewed and approved the Interim Report of the BioPorto Group for the period January 1 to  
March 31, 2025.  
The Interim Report, which is unaudited and has not been reviewed by the Company’s auditors, is presented in accordance with IAS 34 “Interim Financial  
Reporting” as adopted by the EU and additional Danish disclosure requirements for interim reports of listed companies.  
In our opinion, the interim report gives a true and fair view of the Group’s financial position as of March 31, 2025, and the results of the Group’s operations  
and cash flows for the period January 1 to March 31, 2025.  
In our opinion the managements review includes a fair review of the development and performance of the business, the results for the period and the  
Group’s financial position in general and describes changes in principal risks and uncertainties that have occurred relative to what was disclosed in the  
consolidated Annual Report for 2024.  
Hellerup, May 8, 2025
Executive Management:  
___________________________  
Peter Mørch Eriksen
CEO
___________________________  
Gry Louise Husby Larsen
CLO
___________________________  
Niels Høy Nielsen
CFO
Board of Directors:  
___________________________  
Jens Due Olsen
___________________________  
Henrik Juuel
__________________________  
Mats Thorén
Chair
Vice Chair
___________________________  
Donna Haire
Interim Report BioPorto, first three months of 2025  
7
 
Interim Financial Statements  
Condensed Consolidated Statements of Loss  
2025 2024 2024  
Jan 1 - Mar 31  
(Unaudited)  
Jan 1 - Mar 31  
(Unaudited)  
Jan 1 - Dec 31  
DKK thousand  
Notes  
3
Revenue  
7,667
2,759
9,461
2,291
36,243
11,713
24,530
30,202
33,533
36,247
(75,452)
2,543
Production costs  
Gross profit  
4,908
7,170
Sales and marketing costs  
Research and development costs  
Administrative costs  
Loss before financial items (EBIT)  
Financial income  
8,106
5,993
17,659
9,933
6,319
9,560
(30,790)
208
(14,702)
286
Financial expenses  
Loss before tax  
645
444
834
(31,227)
3,769
(14,860)
1,307
(73,743)
5,500
Income tax benefit, net  
Net loss  
5
6
(27,458)
(13,553)
(68,243)
DKK  
DKK  
Loss per share (EPS & DEPS)  
(0.06)
(0.04)
(0.17)
Condensed Consolidated Statements of Comprehensive Loss  
2025 2024 2024  
Jan 1 - Mar 31  
(Unaudited)  
Jan 1 - Mar 31  
(Unaudited)  
Jan 1 - Dec 31  
DKK thousand  
Net loss  
(27,458)
(13,553)
(68,243)
Other comprehensive loss:  
Amounts which will be reclassified to the income statement:  
Exchange rate adjustments of investments in subsidiaries  
Other comprehensive loss  
703
(145)
(1,277)
703
(145)
(1,277)
Comprehensive loss  
(26,755)
(13,698)
(69,520)
Interim Report BioPorto, first three months of 2025  
8
 
Condensed Consolidated Balance Sheets  
Assets  
2025 2024 2024  
Mar 31  
Mar 31  
Dec 31  
DKK thousand  
Notes  
(Unaudited)  
(Unaudited)  
Non-current assets  
Property, plant and equipment and intangible assets  
Rights and software  
242
380
276
Property, plant and equipment  
Right-of-use assets  
1,945
6,140
8,327
801
836
2,136
6,579
8,991
Total property, plant and equipment and intangible assets  
2,017
Financial assets  
Lease receivable - Long term  
Deposits  
9
5
1,351
2,229
3,847
7,427
15,754
2,789
1,255
1,307
5,351
7,368
1,707
1,415
-
Non-current tax receivable  
Total financial assets  
Total non-current assets  
3,122
12,113
Current assets  
Inventories  
5,866
7,314
6,362
1,582
3,788
1,161
32,842
58,915
3,271
4,746
5,903
1,004
3,280
586
4,640
8,187
6,392
1,368
2,448
1,200
59,664
83,899
Trade receivables  
7, 9  
5
Current tax receivable  
Other receivables  
7, 9  
7
Prepayments  
Lease receivable - short term  
Cash and cash equivalents  
Total current assets  
9
9
45,284
64,074
Total assets  
74,669
71,442
96,012
Interim Report BioPorto, first three months of 2025  
9
 
Equity and Liabilities  
2025 2024 2024  
Mar 31  
Mar 31  
Dec 31  
DKK thousand  
Equity  
Notes  
(Unaudited)  
(Unaudited)  
Share capital  
8
8
429,670
-
379,670
-
429,670
Treasury shares  
Exchange-rate adjustments  
Retained earnings  
Total equity  
-
(1,052)
(349)
80
(387,881)
41,440
(338,045)
41,705
(360,840)
67,778
Liabilities  
Non-current liabilities  
Lease obligations  
9
6,851
3,942
7,846
Total non-current liabilities  
6,851
3,942
7,846
Current liabilities  
Current portion of lease obligations  
Trade payables  
9
9
3,385
6,049
-
2,588
6,408
79
3,344
5,706
-
Tax payables  
Other accrued liabilities  
Total current liabilities  
10  
16,944
26,378
16,720
25,795
11,338
20,388
Total liabilities  
33,229
74,669
29,737
71,442
28,234
96,012
Total equity and liabilities  
Interim Report BioPorto, first three months of 2025  
10  
 
Condensed Consolidated Statement of Changes in Equity (Unaudited)  
Share  
Capital  
Share  
Premium  
Treasury  
Shares  
Accumulated  
Deficit  
AOCI  
Total  
Amounts in DKK thousand  
Balance at December 31, 2024  
Other comprehensive loss  
Transaction with owners:  
Share-based compensation  
429,670
-
13
(360,840)
(1,052)
67,778
703
-
-
-
-
703
-
-
-
-
-
-
417
-
-
417
Net loss  
(27,458)
(27,458)
41,440
Balance at March 31, 2025  
429,670
-
13
(387,881)
(349)
Share  
Capital  
Share  
Premium  
Treasury  
Shares  
Accumulated  
deficit  
AOCI  
Total  
Amounts in DKK thousand  
Balance at December 31, 2023  
Other comprehensive loss  
Transaction with owners:  
Share-based compensation  
379,670
-
13
(319,735)
225
60,160
(145)
-
-
-
-
(145)
-
-
-
-
-
-
(4,757)
-
-
(4,757)
Net loss  
(13,553)
(13,553)
Balance at March 31, 2024  
379,670
-
13
(338,045)
80
41,705
Interim Report BioPorto, first three months of 2025  
11  
 
Condensed Consolidated Statement of Cash Flows  
2025 2024 2024  
Mar 31  
Mar 31  
Dec 31  
DKK thousand  
Notes  
(Unaudited)  
(Unaudited)  
Loss before financial items  
(30,790)
(14,702)
(75,452)
Adjustments:  
Depreciation and amortization  
Share based compensation expenses  
Other non-cash items  
664
417
95
-
618
(4,757)
3,878
-
2,382
(875)
4
(1,400)
(984)
Remeasurement of lease  
Changes in operating assets and liabilities:  
Inventories  
(1,111)
819
219
(2,406)
(497)
(864)
(5,847)
(1,199)
(5,542)
(89,781)
Trade receivables  
Trade payables  
343
Other operating assets and liabilities, net  
Cash flows from operations  
5,424
(24,139)
(2,816)
(20,463)
Financial income, received  
Financial expenses, paid  
Tax refund, net  
62
(29)
41
(275)
-
1,641
(381)
-
4,938
Cash flows from operating activities  
(24,106)
(20,697)
(83,583)
Purchase of property, plant and equipment  
Purchase of financial assets  
(1,368)
(825)
-
-
-
(350)
(165)
921
Proceeds from financial assets  
Proceeds from sublease  
-
361
299
299
781
Cash flows from investing activities  
(1,832)
1,187
Proceeds from rights issue  
-
-
-
-
81,400
(3,387)
(2,547)
75,466
Cost related to Issue of new shares  
Repayments of lease obligation  
Cash flows from financing activities  
(965)
(965)
(919)
(919)
Net cash flows for the period  
(26,903)
59,664
81
(21,317)
66,402
199
(6,930)
66,402  
192
Cash and cash equivalents at beginning of period  
Effect of exchange rate changes on cash  
Cash and cash equivalents end of period  
32,842
45,284
59,664
Interim Report BioPorto, first three months of 2025  
12  
 
Notes to Interim Condensed  
Consolidated Financial Statements  
(Unaudited)  
1. Basis of reporting  
Basis of preparation  
This Interim Report and the accompanying unaudited interim condensed consolidated financial statements include the accounts of BioPorto A/S and its  
subsidiaries (“BioPorto” or “the Group”). All significant intercompany accounts and transactions have been eliminated in consolidation. The accompanying  
unaudited interim condensed consolidated financial statements have been prepared in accordance with IAS 34 “Interim Financial Reporting” as issued by  
the International Accounting Standards Board (IASB) and adopted by the EU, and the additional Danish regulations for the presentation of quarterly interim  
reports by listed companies. Certain information and footnote disclosures normally included in the consolidated financial statements prepared in  
accordance with IFRS Accounting Standards (“IFRS”) as adopted by the EU have been condensed or omitted pursuant to such rules and regulations. The  
accompanying unaudited interim condensed consolidated financial statements should be read in conjunction with the audited consolidated financial  
statements and notes thereto contained in BioPorto’s Annual Report for the fiscal year ended December 31, 2024.  
The Company’s assessment as to the adequacy of liquidity relies inter alia on assumptions and significant judgements (in addition to those matters  
discussed cf. Note 2) applied in the Companys budgets and forecasts as well as customary sensitivities, existing capital resources and assumptions  
concerning the timing, costs and resources required to undertake the Company’s strategic priorities and tactical decisions. We have allocated resources  
and significant efforts regarding the US clinical commercial launch of ProNephro AKI (NGAL) for pediatric and young adults, commercialization activities  
for NGAL tests under CE Mark and Antibodies in Europe, supply chain management, and ongoing R&D, all of which under current circumstances remain  
difficult to predict.  
The Company assessed its liquidity and capital resources based on a sufficient cash in fallback scenario should no additional financing be added in the next  
four quarters and concluded that these are adequate to fund operations considering a twelve-month period from the balance sheet date due to the  
Company’s ability to scale back its strategic initiatives based on facts and circumstances. The Company continues to monitor its liquidity needs, manage its  
costs, and investigate its financing options.  
In the event that the Company’s strategic priorities and tactical decisions, commercialization activities for NGAL tests in the US, under CE Mark and  
Antibodies, and ongoing R&D are more positive than expected, the Company may choose to accelerate projects and/or increase spending, in which case  
the Company may be required or may choose to raise additional capital prior to the twelve month period after the date of this Interim Report.  
The unaudited interim condensed consolidated financial statements are presented in Danish Kroner (DKK), which is considered the primary currency of  
the Group’s activities and the functional currency of the parent company.  
Accounting policies  
The accounting policies used in the unaudited interim condensed consolidated financial statements are consistent with those used in the consolidated  
financial statements for 2024 and in accordance with the recognition and measurement policies of IFRS. Certain comparative figures have been reclassified  
to conform to the current period’s presentation.  
As of March 31, 2025, the Group has implemented all new or amended IFRS accounting standards and interpretations as adopted by the EU and applicable  
for the 2025 financial year. None of the new or amended standards or interpretations are assessed to have a material impact on the unaudited condensed  
consolidated financial statements. The Group has not implemented any new or modified standards and interpretations that are not yet effective. The new  
or modified standards and interpretations will be implemented when they become mandatory. They are not presently expected to have a material impact  
on the Group’s consolidated financial statements.  
The new IFRS 18 is expected to change the presentation of the Income statement and to differentiate between earnings from operating activities,  
investment activities and financing activities. IFRS 18 will also add additional disclosures but will not change any accounting policies on recognition and  
measurement, hence it will not change reported net results. IFRS 18 will come into effect in 2027 or later.  
2. Critical accounting estimates and judgments  
The calculation of the carrying amounts of certain assets and liabilities requires an estimate of how future events will affect the value of such assets and  
liabilities at the balance sheet date. Estimates material to the financial reporting are made in the calculation of, inter alia, development costs, incentive  
schemes, inventories, accounts receivable, and deferred taxes.  
The estimates made are based on assumptions that Management finds reasonable given the circumstances, but which are inherently uncertain and  
unpredictable. The assumptions may be incomplete or imprecise and unexpected events or circumstances may arise. In addition, the Company is subject  
Interim Report BioPorto, first three months of 2025  
13  
 
to risks and uncertainties that may cause actual results to deviate from the estimates. Such estimates comprise judgments made on the basis of the most  
recent information available at the reporting date. It may be necessary to change previous estimates as a result of changes to the assumptions on which  
the estimates were based or due to supplementary information, additional experience or subsequent events.  
Similarly, the value of assets and liabilities often depends on future events that are somewhat uncertain. In that connection, it is necessary to set out e.g.,  
a course of events that reflects Management’s assessment of the most probable course of events. Special risks to BioPorto are described in the Annual  
Report as of and for the year ended December 31, 2024. The significant judgements made by Management in applying the Group’s accounting policies and  
the key sources of estimation uncertainty were not materially different from those that applied to the consolidated financial statements, C.f. the Annual  
Report as of and for the year ended December 31, 2024.  
3. Business area reporting  
2025 2024 2024  
GEOGRAPHIC DISTRIBUTION  
Jan 1 - Mar 31  
(Unaudited)  
Jan 1 - Mar 31  
(Unaudited)  
Jan 1 - Dec 31  
DKK Thousand  
North America  
Europe  
5,805  
1,431  
431  
4,734  
2,914  
1,813  
-
20,634  
10,237  
5,372  
-
Asia  
Other regions  
Revenue  
-
7,667  
9,461  
36,243  
2025 2024 2024  
PRODUCT GROUPS  
DKK Thousand  
Jan 1 - Mar 31  
(Unaudited)  
Jan 1 - Mar 31  
(Unaudited)  
Jan 1 - Dec 31  
NGAL tests  
4,604  
2,505  
526  
6,108  
2,673  
662  
23,054  
10,783  
2,269  
137  
Antibodies  
ELISA kits  
Royalty and other revenue  
Revenue  
32  
18  
7,667  
9,461  
36,243  
4. Share-based payment  
For the purpose of motivating and retaining Management and key staff and aligning their interests with those of its shareholders, BioPorto A/S uses  
warrants as an incentive scheme. The arrangements, which are exercised by the issuance of new shares (equity-settled share-based payment transaction),  
entitle the recipient to subscribe for new shares in the parent company at a price defined on the date of grant.  
In the first three months of 2025, share-based compensation totaled an expense of DKK 0.4 million compared to an income of DKK 4.8 million for the prior  
year period. The warrant terms are included in the Company’s Articles of Association, which can be found at www.bioporto.com. Upon vesting, each  
warrant entitles the recipient to subscribe for one share in BioPorto A/S.  
Interim Report BioPorto, first three months of 2025  
14  
 
5. Taxes  
The Group has a deferred tax asset. However, Management has found that it is not sufficiently probable that the tax asset can be utilized in the foreseeable  
future. Management has therefore decided not to recognize the deferred tax assets on the balance sheet, cf. Note 2. The deferred tax asset is of indefinite  
duration. As of the most recent year-end, December 31, 2024, the gross value of the deferred tax asset prior to the valuation allowance was DKK 105.4  
million.  
Taxes receivable represent refunds of previous US federal tax liabilities and tax credits held by its Danish entities associated with the Company’s investment  
in research and development.  
6. Loss per share  
2025 2024 2024  
Jan 1 - Mar 31  
(Unaudited)  
Jan 1 - Mar 31  
(Unaudited)  
Jan 1 - Dec 31  
DKK thousand (except where noted)  
Loss for the period  
(27,458)  
(13,553)  
(68,243)  
BioPorto Group's share of loss  
(27,458)  
(13,553)  
(68,243)  
Weighted average number of shares (in thousand)  
429,670  
(13)  
379,670  
(13)  
405,763  
(13)  
Weighted average number of treasury shares (in thousand)  
Weighted average number of shares in circulation basic and diluted (in thousand)  
Loss per share (EPS) basic and diluted, DKK  
429,657  
(0.06)  
379,657  
(0.04)  
405,750  
(0.17)  
Warrants outstanding were excluded from the calculation of loss per share because the effect would have been anti-dilutive.  
7. Receivables  
For receivables that mature within one year after the end of the financial year, the nominal value is considered to correspond to the fair value.  
2025 2024 2024  
Mar 31  
Mar 31  
Dec 31  
DKK thousand  
(Unaudited)  
(Unaudited)  
Trade receivables  
7,432  
4,810  
8,251  
Other receivables  
1,582  
3,788  
(118)  
1,004  
3,280  
(64)  
1,368  
2,448  
(64)  
Prepayments  
Write-down for bad debt  
Receivables at amortized costs  
12,684  
9,030  
12,003  
Interim Report BioPorto, first three months of 2025  
15  
 
A write-down for bad debts is recognized to reduce the carrying amount of trade receivables by the value which is impaired due to risk of loss.  
AS OF MARCH 31, 2025  
Expected  
Trade  
DKK thousand  
credit loss rate  
receivables  
Expected loss  
Total  
3,057  
Not due  
0.1%  
0.1%  
3,061  
4
1 - 30 days overdue  
31 - 60 days overdue  
61 - 90 days overdue  
More than 90 days overdue  
As of March 31, 2025  
3,230  
512  
3
1
3,227  
511  
0.2%  
0.0%  
399  
2
397  
47.0%  
230  
108  
118  
122  
7,432  
7,314  
AS OF MARCH 31, 2024  
DKK thousand  
Expected  
credit loss rate  
Trade  
receivables  
Expected loss  
Total  
Not due  
0.3%  
0.3%  
4,046  
11  
1
4,035  
289  
1 - 30 days overdue  
31 - 60 days overdue  
61 - 90 days overdue  
More than 90 days overdue  
As of March 31, 2024  
290  
135  
0.0%  
-
135  
0.4%  
249  
1
248  
56.7%  
90  
51  
64  
39  
4,810  
4,746  
8. Share capital  
As of March 31, 2025, the share capital consists of 429,670,461 shares of DKK 1.00 each. The share capital has been paid up in full. The shares have not  
been divided into classes and carry no special rights. As of March 31, 2025, and 2024, and December 31, 2024, the Company held 13,000 treasury shares  
representing less than 0.01% of outstanding shares as of each date with nominal value of DKK 13,000. As of March 31, 2025, BioPorto A/S is not authorized  
to acquire treasury shares. BioPorto A/S did not acquire treasury shares during the three months ended March 31, 2025, or the year ended December 31,  
2024.  
Interim Report BioPorto, first three months of 2025  
16  
 
9. Financial risks and financial instruments  
Financial instrument categories  
2025 2024 2024  
Mar 31  
Mar 31  
Dec 31  
DKK thousand  
(Unaudited)  
(Unaudited)  
Trade receivables  
7,314  
4,746  
8,187  
Other receivables  
1,582  
1,161  
1,004  
586  
1,368  
1,200  
Lease receivable - Short term  
Lease receivable - Long term  
Cash and cash equivalents  
Financial assets at amortized costs  
1,351  
2,789  
45,284  
54,409  
1,707  
32,842  
44,250  
59,664  
72,126  
2025 2024 2024  
Mar 31  
Mar 31  
Dec 31  
DKK thousand  
(Unaudited)  
(Unaudited)  
Lease liabilities  
10,236  
-
6,530  
11,190  
Other non-current liabilities  
Trade payables  
-
6,408  
-
5,706  
6,049  
16,285  
Financial liabilities at amortized costs  
12,938  
16,896  
Financial liabilities  
Trade payables generally fall due within one year after the end of the financial year. Their carrying amount is assumed to equal the fair value.  
Currency risk  
The Group’s presentation currency is DKK, but part of its activities is denominated in currencies other than DKK, primarily USD and EUR. Consequently,  
there is a risk of exchange rate fluctuations having an impact on the Group’s reported results.  
The Group is exposed to currency risks through sales, production, R&D contracts, and payroll denominated in currencies other than DKK. The Group is  
subjected to transaction risk related to sales and purchases in foreign currencies, and translation risk when translating foreign entities into the Group’s  
presentation currency.  
Interim Report BioPorto, first three months of 2025  
17  
 
2025 2024 2024  
B/S CURRENCIES PERCENTAGES  
DKK thousand  
Mar 31  
Mar 31  
Dec 31  
(Unaudited)  
(Unaudited)  
Inventory  
DKK  
100%  
100%  
100%  
Trade receivables  
USD  
31%  
69%  
-
44%  
56%  
-
30%  
68%  
2%  
EUR  
Other  
Cash and cash equivalents  
DKK  
USD  
EUR  
89%  
8%  
92%  
5%  
93%  
6%  
3%  
3%  
1%  
Trade payables  
DKK  
31%  
64%  
5%  
-
48%  
43%  
6%  
53%  
29%  
17%  
1%  
USD  
EUR  
Other  
3%  
Based on its transaction volume, the Group has determined not to hedge its USD exposure. As the DKK is pegged to the EUR, hedging of the Company’s  
transactions in EUR is not necessary.  
Interest rate risk  
The Group has interest rate exposure because substantially all of its assets consist of bank deposits. A one percent change in interest rate could result in a  
change in interest income of approximately DKK 0.3 million based on the interest-bearing accounts portion of the DKK 32.8 million cash and cash  
equivalents as of March 31, 2025.  
Credit risk  
The Group’s credit risk is primarily associated with trade receivables. Cash and cash equivalents are deposited with major Nordic and US banks. The financial  
situation and ability of customers to pay trade receivables are regularly evaluated, with payment upon placement of an order required if ability-to-pay is  
evaluated to be low. Expected credit losses are estimated by analyzing trade receivables by customer type and days past due. An estimated loss percentage  
is calculated based on historical credit losses and specific customer circumstances. Trade receivables are written off when there is no reasonable  
expectation of recovery.  
Liquidity risk  
In connection with BioPorto’s ongoing financing of operations, efforts are made to ensure sufficient financial resources are available. BioPorto’s cash and  
cash equivalents totaled DKK 32.8 million and DKK 59.7 million as of March 31, 2025, and December 31, 2024, respectively.  
Free funds are placed in deposits to maintain flexibility.  
Capital structure  
Management regularly assesses whether the Group’s capital structure properly serves the interests of the Group and its shareholders.  
Interim Report BioPorto, first three months of 2025  
18  
 
10. Other accrued liabilities  
2025 2024 2024  
Mar 31  
Mar 31  
Dec 31  
DKK thousand  
(Unaudited)  
(Unaudited)  
Accrued incentive compensation  
Accrued board fee  
3,773  
1,378  
3,290  
-
1,937  
1,253  
4,621  
2,926  
489  
2,602  
1,396  
4,416  
-
-
1,599  
1,014  
892  
Accrued vacation  
Accrued professional and consulting fees  
Accrued clinical trial costs  
Accrued supplier costs  
2,384  
2,863  
1,681  
16,720  
2,926  
-
Accrued severance costs  
Accrued expenses - Other  
Other accrued liabilities  
1,945  
16,944  
1,617  
11,338  
11. Commitments and contingencies  
All of the Company’s existing and proposed diagnostic products are regulated by the FDA and similar regulatory bodies in other countries and/or regions.  
Most aspects of development, production, and marketing, including product testing, authorizations to market, labeling, promotion, manufacturing, and  
record keeping, are subject to regulatory review.  
After marketing approval has been granted, the Company must continue to comply with governmental regulations. Failure to comply with applicable  
requirements can lead to sanctions, including withdrawal of products from the market, recalls, refusal to authorize government contracts, product seizures,  
civil money penalties, injunctions, and criminal prosecution.  
From time to time the Company may become involved in legal proceedings or may be subject to claims arising in the ordinary course of its business.  
Although the results of litigation and claims cannot be predicted with certainty, the Company currently believes that the final outcome of these ordinary  
course matters will not have a material adverse effect on its business, operating results, financial condition or cash flows. Regardless of the outcome,  
litigation can have an adverse impact on the Company because of defense and settlement costs, diversion of management resources, and other factors.  
12. Related parties  
Related parties with significant interests  
Other related parties of BioPorto with significant interests include the Board of Directors, the Executive Management, and their close family members.  
Related parties also include companies in which these persons have control or significant interests.  
Transactions with related parties  
Other than ordinary management and Board of Director remuneration, the company did not have any transactions with related parties in the first three  
months of 2025.  
13. Subsequent events  
On April 15, 2025, the Company announced that a private placement of 25,000,000 new shares has been completed. The gross proceeds for the new shares  
is DKK 33.5 million.  
Interim Report BioPorto, first three months of 2025  
19  
 
BioPorto is an in vitro diagnostics company focused on saving lives and improving  
the quality of life with actionable biomarkers tools designed to help clinicians  
make changes in patient management. The Company uses its expertise in  
antibodies and assay development, as well as its platform for assay  
development, to create a pipeline of novel and compelling products that focus  
on conditions where there is significant unmet medical need, and where the  
Company’s tests can help improve clinical and economic outcomes for patients,  
providers, and the healthcare ecosystem.  
The Company’s flagship products are based on the NGAL biomarker and  
designed to aid in the risk assessment and diagnosis of Acute Kidney Injury, a  
common clinical syndrome that can have severe consequences, including  
significant morbidity and mortality, if not identified and treated early. With the  
aid of NGAL levels, physicians can identify patients potentially at risk of AKI more  
rapidly than is possible with current standard of care measurements, enabling  
earlier intervention and more tailored patient management strategies. The  
Company markets NGAL tests under applicable registrations including CE mark  
in several countries worldwide.  
BioPorto has facilities in Copenhagen, Denmark and Boston, MA, USA. The shares  
of
BioPorto A/S
are listed on the Nasdaq Copenhagen stock exchange. For more  
information visit www.bioporto.com.  
www.bioporto.com  
BioPorto A/S  
BioPorto, Inc.  
Tuborg Havnevej 15, ground floor  
DK-2900 Hellerup  
Denmark  
117 Kendrick Street, Suite 300  
Needham, MA 02494  
USA  
CVR DK-17500317  
Interim Report BioPorto, first three months of 2025  
20