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    CROSSJECT presents its financial results and key highlights for the first half of 2025

    Press release

    CROSSJECT presents its financial results and key highlights for the first half of 2025

    • Cash position: €6.3 million, compared to €7.0 million as of December 31 2024, demonstrating the Company's excellent control of its resources.
    • Stable R&D investments and a €3.1 million increase in R&D reimbursements from BARDA1 for the first half of 2024, to €6.5 million, in line with the focus on regulatory development and batch manufacturing related to the registration of ZEPIZURE.
    • The company continued to make progress toward BARDA's submission of its Emergency Use Authorization (EUA) application for ZEPIZURE.

    Dijon, France, September 24, 2025 10:00 p.m. CET -- CROSSJECT (ISIN: FR0011716265; Euronext: ALCJ), a specialty pharmaceutical company developing products for emergency situations based on its proprietary ZENEO needle-free auto-injector technology, today announced its financial results for the first half of the year ended June 30, 2025, and provided an update on its business highlights for the first half of 2025.

    During this period, CROSSJECT continued its regulatory activities in conjunction with the U.S. Biomedical Advanced Research and Development Authority (BARDA) with the aim of obtaining regulatory approvals for ZEPIZURE in the United States as soon as possible.

    In this context, in June, and as announced in May 2025, CROSSJECT and its CDMO partner EUROFINS produced the validation batches, the data from which form part of the EUA dossier, and organized the manufacture of batches so that they would be available at the time of the EUA evaluation.

    Beyond the reference period ending June 30, 2025, CROSSJECT is continuing its activities related to the registration of ZEPIZURE, in particular:

    • The company and BARDA used the summer period to draft and review the detailed,
    • In September, BARDA conducted mock audits to prepare the company for potential FDA inspections.

    In addition, in September, the Company obtained an €11.3 million extension of R&D funding under its contract with the U.S. government.

    Other significant events also occurred after the close of the financial year:

    • The company obtained a new credit line of €750,000 from a new banking partner,
    • The company obtained renewal of its ISO 13485 certification for all of its sites (Dijon and Gray),
    • The company also saw its Good Manufacturing Practices (GMP) certificate extended.

    In the current macroeconomic context, the company and its advisors believe that it is not currently exposed to any impact from increases in European customs duties on shipments to the United States destined for BARDA.

    We would also like to point out that, in preparation for the increase in production volumes when its product portfolio is commercialized, the company finalized the development and introduction of its ZENEO Nest module, the latest innovation from the ZENEO Factory, during the first half of the year. ZENEO Nest facilitates and accelerates aseptic filling operations on high-speed automated lines available at many CDMOs.

    Finally, as part of its direct marketing strategy in the United States, the Company continued to strengthen the potential of ZEPIZURE in collaboration with opinion leaders in epilepsy and emergency medicine.

    "Throughout 2025, CROSSJECT continued to make decisive progress toward filing the EUA application for ZEPIZURE. We express our gratitude to BARDA for its diligence and consistency in reviewing the data and its attention to our manufacturing tool. Pragmatic and committed to secure the registration of ZEPIZURE as quickly as possible, BARDA also granted us a major increase (of more than $11 million) in its contribution", said Patrick ALEXANDRE, Chairman of the Executive Board of CROSSJECT.

    See also Appendices 1 (income statement), 2 (balance sheet assets) and 3 (balance sheet liabilities).

    1 Contract No. 75A50122C00031 with the Department of Health and Human Services; Administration for Strategic Preparedness and Response; Biomedical Advanced Research and Development Authority.

    About CROSSJECT

    CROSSJECT SA (Euronext: ALCJ; www.crossject.com) is an emerging specialty pharmaceuticals company developing medicines for emergency situations harnessing its award-winning needle-free auto-injector ZENEO platform. CROSSJECT is in advanced regulatory development for ZEPIZURE, an epileptic rescue therapy, for which it has a $60 million contract* with BARDA. The Company’s versatile ZENEO platform is designed to enable patients or untrained caregivers to easily and instantly deliver a broad range of emergency drugs via intramuscular injection on bare skin or even through clothing. The Company’s other products in development include mainly solutions for allergic shocks and adrenal insufficiencies, as well as therapies and other emergency indications.

    • This project has been supported in whole or in part with federal funds from the US Department of Health and Human Services; Administration for Strategic Preparedness and Response; BARDA, under contract number 75A50122C00031.

    For more information, please contact :

       
     

    Investor relations
    investors@crossject.com
     

    Press contact
    melanie.voisard@buzzetcompagnie.com

    Appendix 1

    Income statement H1 2025 vs H1 2024

    (in 000’s euros) 30/06/2025 30/06/2024
    Revenues 8 038 5 766
    BARDA R&D reimbursements 6 584 3 064
    Capitalized production (1) 1 483 1 565
    Stored production -96 354
    Other incomes 67 784
         
    Operating expenses -13 177 -12 485
    Purchases of raw materials and other supplies -586 -695
    Other purchases and external expenses -5 356 -5 005
    Personnel expenses -4 049 -3 950
    Taxes and duties -147 -100
    Depreciation, amortization -2 630 -2 517
    Other expenses -409 -218
    Operating loss -5 139 -6 719
    Net financial expenses -1 143 -994
    Exception incomes / expenses -140 -330
    Research tax credit 1 555 1 641
    Net loss -4 869 -6 402

    Accounts approved by the Executive Board on 24 September 2025 and presented to the Supervisory Board on the same day.

    For the first half of 2025, CROSSJECT's operating loss amounted to €5.1 million, an improvement of €1.5 million compared to the loss of €6.7 million for the same period in 2024. This positive change reflects:

    • A sharp increase in reimbursements from BARDA, amounting to €6.5 million in the first half of 2025, compared with €3.1 million in 2024. These reimbursements reflect a concentration and acceleration of BARDA's R&D activities, including the manufacture of multiple batches during the period related to the ZEPIZURE application. The coverage ratio of our operating expenses is higher than previously.
    • Good control of total operating expenses, which rose to €13.2 million compared with €12.5 million in the first half of 2024.

    The company's net loss amounted to €4.9 million in the first half of 2025, compared with €6.4 million in the first half of 2024.

    As part of its multiple activities, and as evidenced by the extension recently obtained from BARDA and its new bank financing, the company continues to continuously evaluate its dilutive and non-dilutive financing options.

    Appendix 2

    Assets, 30 June 2025 vs 31 December 2024

    (in 000’s euros) 30/06/2025 31/12/2024

    FIXED ASSETS

    R&D 8 908 9 591
    Patents and trademarks 0 0
    Other intangible assets 1 6
    Property, plant and equipment 2 129 2 126
    Asset under construction 3 600 2 924
    Financial assets 986 1 041
    TOTAL FIXED ASSETS 15 674 15 687

    CURRENT ASSETS

    Raw materials, other supplies 2 015 1 970
    Work in progress 1 188 1 448
    Other receivables 4 980 4 295
    Cash and cash equivalents 6 338 7 036
    Prepaid / deferred expenses 1 179 1 131
    TOTAL CURRENT ASSETS 15 700 15 180
    TOTAL ASSETS 31 375 31 567

    Appendix 3

    Liabilities and Shareholders’ Equity - 30 June 2025 vs 31 December 2024

    (en 000’s euros) 30/06/2025 31/12/2024

    SHAREHOLDERS’ EQUITY

    Capital 5 077 4 554
    Share premium 6 133 7 192
    Regulated reserve 0 0
    Retained earnings
    • 8 391
    • 2 596
    Loss for the period
    • 4 868
    • 12 795
    Investment subsidies 952 972
    TOTAL SHAREHOLDERS’ EQUITY
    • 1 097
    • 2 673
    Conditional advances 4 750 5 391
    Provision for contingencies and charges 1 047 910

    LIABILITIES

    Convertible bond 6 597 5 478
    Financial debt 11 077 12 874
    Other liabilities 2 608 2 717
    Trade payables 4 248 4 554
    Tax and social security liabilities 1 577 1 770
    Deferred income 588 616
    TOTAL LIABILITIES 26 675 27 939
    TOTAL LIABILITIES AND SHAREHOLDERS” EQUITY 31 375 31 567

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    CROSSJECT presents its financial results and key highlights for the first half of 2025 Press release CROSSJECT presents its financial results and key highlights for the first half of 2025 Cash position: €6.3 million, compared to €7.0 million as of December 31 2024, demonstrating the Company's excellent control of its resources. …