공시 • May 08
Spermosens AB (publ) announced that it expects to receive SEK 4.85 million in funding Spermosens AB (publ) has announced a private placement to issue units at the price of 15% discount to VWAP for the gross proceeds of SEK 4,850,000 on May, 2026. The transaction involves the existing share holder investor participation and CEO Tore Duvold via Duvold Holding ApS for SEK 0.1 million Chairman Ulrik Spork for SEK 0.1 million Mount Nebo Investments LLC for SEK 2.0 million Seven additional shareholders for SEK 2.65 million combined. Each unit will consist of one share and one warrant issued free of charge. The warrants will have a term of three years and entitle the holder to subscribe for one new share at a subscription Exercise price of SEK 0.025 per share. The warrants may be exercised during one week prior to each half-year during the term. The transaction is approved by board of directors and subject to approval of shareholders at the AGM on June 18, 2026 for authorization to issue securities. 공시 • May 01
Spermosens AB Reports Clinical Validation Study of Juno-Checked Generation 3 System on Track Spermosens AB reported that the clinical validation study of the JUNO-Checked Generation 3 system at the Reproductive Medicine Center (RMC) in Malmö has started and is progressing according to plan. Seven patients have been successfully tested to date. The study started in April 2026, in line with the previously communicated timeline. The Company completed development of the Generation 3 system and planned to initiate patient recruitment at the RMC in Malmö. The study is now underway, and the first weeks confirm that patient recruitment and clinical routines are progressing as expected, with the JUNO-Checked Generation 3 system performing as intended. The study includes couples undergoing standard IVF treatment due to unexplained infertility, where semen samples show normal parameters based on currently available sperm analysis methods. Unlike standard semen analysis, JUNO-Checked measures whether sperm cells can bind to the egg, which is essential for fertilization. The aim of the study is to confirm that the Generation 3 system can identify the cause of fertilization failure in cases where standard testing shows no abnormalities. Completion of the study is expected by the end of 2026. Spermosens aims to bring JUNO-Checked to the global market through licensing or partnership agreements with established companies. Successful completion of the clinical validation study is a key step toward commercialization. 공시 • Apr 10
Spermosens AB Completes Development of JUNO-Checked Generation 3 and Initiates Clinical Validation Study Spermosens AB announced that development of the JUNO-Checked Generation 3 system is now complete. This innovative sensor system meets the performance standards necessary for a commercially viable product. The Company is preparing to initiate patient recruitment for a clinical validation study at the Reproductive Medicine Center (RMC) in Malmö. The development of JUNO-Checked Generation 3 has focused on the specific needs of clinics and laboratories. This system features significant key technical improvements, such as significantly shorter analysis times and a more robust sensor design to support high-volume clinical workflows. These enhancements are intended to reduce technical and operational risks for future partners and support integration into existing laboratory environment. The system is designed for compatibility with established laboratory platforms, enabling seamless adoption in clinical practice. The clinical validation study will be conducted at Reproductive Medicine Center (RMC) in Malmö and is designed to validate the performance of the new system in a clinical environment. Patient recruitment is expected to begin shortly. The study focuses on couples undergoing standard IVF due to unexplained infertility, where semen samples are classified as normal in routine testing. The aim is to demonstrate that JUNO-Checked provides additional diagnostic value by identifying sperm-related dysfunctions not detected by conventional methods. Completion of the study is expected by the end of the year. Successful validation is a key step toward registration and commercialization. In line with the Company strategy, Spermosens aims to bring JUNO-Checked to the market through license or co-development agreements. This approach is designed to reduce capital needs and improve the likelihood of a successful market introduction through established companies. JUNO-Checked addresses a global fertility market where improved functional testing is essential to support clinical decisions and improve treatment outcomes for millions of couples. 공시 • Apr 08
Spermosens AB (publ) to Report Q1, 2026 Results on May 07, 2026 Spermosens AB (publ) announced that they will report Q1, 2026 results on May 07, 2026 공시 • Jan 13
Spermosens AB (publ) to Report Fiscal Year 2025 Results on Feb 11, 2026 Spermosens AB (publ) announced that they will report fiscal year 2025 results on Feb 11, 2026 공시 • Dec 10
Spermosens AB Provides Update on Recent Progress and the Next Steps in Its Partner-Driven Commercialization Strategy for Juno-Checked Spermosens AB presents an update on recent progress and the next steps in its partner-driven commercialization strategy for JUNO-Checked. The Company completed a successful clinical study in June 2025, confirming the diagnostic value of JUNO-Checked and continues to build a strong foundation for a partner-led market introduction. Development of Generation 3, the intended commercial version, is progressing and dialogues with potential partners in Europe, the United States, Japan and Australia are advancing. Central to the Company's go-to-market strategy is the establishment of licensing and partnership structures that support regulatory activities, market adaptation and commercial rollout. This update contains forward-looking information about anticipated milestones, timelines and commercialization pathways. Such information reflects current expectations and is subject to risks and uncertainties, as outlined under "Forward-looking information" below. Product development and intellectual property: Spermosens has advanced several key areas: The completed clinical study in 2025 has demonstrated that JUNO-Checked provides relevant diagnostic information by assessing a critical biological step in fertilization not captured by conventional sperm analysis. Patent protection has been strengthened through approvals in multiple key markets. Development of the next-generation JUNO-Checked ("Generation 3") is progressing according to plan. H1 2026: Completion of Generation 3, H2 2026: Start clinical validation of Generation 3, H22026: Signing of partner and/or license agreements, H1 2027: Test and validation activities with partners, H2 2027: Regulatory filings and market preparation activities with partners, H1 2028: Commercial rollout through partners. Partner strategy and collaboration models: Spermosens commercialization strategy focuses on partnering with organizations already established in fertility care, diagnostics and patient-centric reproductive health services. Target partner categories include: Fertility technology companies developing tools to enhance diagnostics and workflows efficiency; Developers of automated laboratory systems used in IVF clinics and andrology laboratories; Fertility clinic groups and sperm banks with advanced in-house laboratory capabilities and interest in new diagnostic tools; Reproductive health platforms integrating diagnostics into patient-centric fertility services. These reflect the types of partners currently engaged in dialogue with Spermosens, including fertility-technology innovators, clinical networks and companies offering patient-centric fertility services. partnership structures: The Company's partnering approach is based on upfront and/or co-financing contributions, milestone payments and royalties on net sales. JUNO-Checked, as a functional sperm-egg binding assay, complements standard sperm analyses and addresses a growing need for more advanced and predictive male-fertility diagnostics. While the entire sperm-analysis market is not directly address for JUNO- checked, the introduction of new diagnostic possibilities may broaden clinical workflows over time. It is not possible to determine at this stage what proportion of the market JUNO-Checked may ultimately address, as this will depend on clinical adoption, regulatory pathways and partner-driven commercialization efforts. JUNO-Checking therefore introduces a novel functional approach to the assessment of male fertility. As such testing becomes available, new clinical use cases may emerge, including unexplained fertility, failed IVF cycles and advanced male-factor assessments, potentially increasing demand for more advanced and predictive diagnostics. Over time, this may extend the long-term opportunity for JUNO-Checking beyond current market definitions, as clinical practice evolves in response to improved diagnostic capabilities. 