Xbrane Biopharma Ab · OMXSTO:XBRANE

Xbrane Biopharma Ab — Q2 2025 Earnings Presentation

19 slides from Xbrane Biopharma Ab's earnings presentation, Aug 26, 2025

  1. Slide 1: Xbrane Biopharma Q2 2025 presentation

    ,RANE BIOPHARMA Q2 2025 present ation a - a mA |

  2. Slide 2: Ximluci launched in 24 countries

    “Ximluci® launched in 24 countries, volume growth +11% in Europe Q2 2025 vs Q1 2025” Wud Martin Amark, CEO August 26" , 2025 MBRANE SCIENCE FOR HIGH QUALITY BIOSIMILARS January - June 2025 Interim Report 26/8/2025

  3. Slide 3: Disclaimer

    Disclaimer You must read the following before continuing, The following applies to this document and the information provided in this presentation by Xbrane Biopharma AB (publ) (the "Company’) or any person on behalf of the Company and any ‘other material distributed or statements made in connection

  4. Slide 4: Presenters

    Presenters P Martin Amark Jane Benyamin CEO CFO MBRANE SCIENCE FOR HIGH QUALITY BIOSIMILARS January - June 2025 Interim Report 26/8/2025

  5. Slide 5: Ximluci launched across 24 countries

    Ximluci® – Launched across 24 countries Ximluci® launched by STADA in 24 countries Co-Development & Commercialization Partnership with STADA Partnership with STADA signed in 2018. STADA are granted the commercial rights to Ximluci® globally  Global generics and biosimilar specialist with including

  6. Slide 6: Ximluci currently at 8% volume market share in Europe

    Ximluci® – Currently at 8% volume market share in Europe Profit split to Xbrane and growth in vials sold by STADA Commentary  Volume growth Q2 2025 vs. Q1 2025 in Europe 11%, across all markets -8% due to quarterly variability in launch shipments to MENA countries  Total profit generation by Xbran

  7. Slide 7: Lucamzi upcoming US FDA BsUFA date October 21st

    Lucamzi – upcoming US FDA BsUFA date October 21st Xbrane & STADA partner with Valorum US Commercialization Partnership Xbrane and STADA license US commercial rights to Valorum Biologics. Valorum will be responsible for sales,  Biosimilar commercialization marketing and commercial efforts in the US

  8. Slide 8: Lucamzi US poses a significant opportunity

    Lucamzi – US poses a significant opportunity US retinal anti VEGF: USD 10 billion market Commentary ~8 million units  Lucentis biosimilars covered under Medicare Part B with 20% 100% patient co-payment  Reimbursement based on ASP* + 6-8% of originator ASP 80%  Dynamic which favors new biosimilar

  9. Slide 9: Xdivane CTA approval in first country triggering €2m milestone

    Xdivane – CTA approval in first country triggering €2m milestone (in Q3) 2024 2025 2026 2027 2028 2029 2030 Commercialization Milestone payment to Milestone payment to Xbrane Xbrane LoE US LoE Europe Production of clinical material Pivotal clinical trial MAA / BLA  Successful scale-up to  Single p

  10. Slide 10: Xdivane +1 billion SEK annual profit sharing potential

    Xdivane – +1 billion SEK annual profit sharing potential for Xbrane US biosimilar volume market share vs. reference product Commentary  Oncology biosimilars have been well received with average penetration of 75% at year 3 post launch in US  Sold via hospital channel in US under Medicare Part B re

  11. Slide 11: Jan-June Interim Report 2025 Financials

    GAR IMM7F Jan-June Interim Report 2025 Financials Ha Sd 3 a HT), | i Z MUBRANE SCIENCE FOR HIGH QUALITY BIOSIMILARS

  12. Slide 12: Net Revenues (Quarter by Quarter)

    Net Revenues (Quarter by Quarter) Net revenue Commentary on 5) SEK m Q2'24 Q3'24 0424 125225 Gross margin 100,0 140% % > Revenue Q2 2025 ~ 39.9 MSEK, Gross Margin 100% 126% MSEK Revenue Q2 2024 ~ 52.0 MSEK 120% 80,0 100% ; gq > Milestone attributable to the license agreement with Intas Pharmaceutica

  13. Slide 13: Company Expenses (G&A and R&D) by Quarter

    Company Expenses (G&A and R&D inc. capitilized R&D) by Quarter SEK m Q2 '24 Q3 124 Q4'24 Q1'25 Q2'25 0,0 98 10. “10 -10,0 18,3 -20,0 > Administration expenses amounted to 18.3 MSEK for Q2 en whereof 9 MSEK corresponding to non-recurring items ~ connected to the transaction with Alvotech -40,0 -50,0

  14. Slide 14: Cash flow Q2-25

    Cash flow Q2-25  275 -5   -153 -90  25 -47 6 

  15. Slide 15: Cash and Cash Equivalents / Operating Cash Flow

    Cash and Cash Equivalents Operating Cash Flow

  16. Slide 16: Q2 2025, Key Take-Aways

    Q2 2025, Key Take-Aways Ximluci® launched in 24 countries, volume growth in Europe +11% Q2 2025 vs Q1 2025 Xdivane progressing according to plan, triggering €2m milestone payment (in Q3) Strategic sale to Alvotech has resulted in significant reduction of debt and reduced cost structure Directed shar

  17. Slide 17: Key Priorities for 2025 and 2026

    Key Priorities for 2025 and 2026 Upcoming Ximluci US FDA BsUFA date October 21st and ongoing preparations for US launch Support STADA in continued penetration of Europe/MENA market for retinal anti-VEGFs including resumed commercial manufacturing during H2 2025 Initiatives to reduce Ximluci producti

  18. Slide 18: Business Concept

    BUSINESS CONCEPT Xbrane develops biosimilars of difficult-to- manufacture and often very expensive original drugs VISION To become a world-leading scientifically-based biosimilar developer of cost-effective drugs for which there is a significant medical need OBJECTIVE To contribute to everybody havi

  19. Slide 19: Jan - June 25 Interim Report

    MUBRANE SCIENCE FOR HIGH QUALITY BIOSIMILA January - June 2025 Interim Report

Xbrane Biopharma — Q2 2025 Earnings Presentation on 6ix