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Xbrane Biopharma (XBRANE) investor relations material
Xbrane Biopharma Q1 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Ximluci, a LUCENTIS biosimilar, launched in 24 countries in Europe and the Middle East, maintaining an 8% market share by volume in Europe as of March 2026, with profit sharing through a partnership with STADA.
Ximluci BLA was resubmitted to the FDA in April 2026 after addressing manufacturing site deficiencies, with a decision expected in November 2026.
Xdivane, an OPDIVO biosimilar candidate, is progressing as planned, with clinical trials initiated and FDA submission targeted for H2/Q4 2027 and potential launch in early 2029.
Agreement with Intas revised: Intas will partly finance Xdivane’s CMC activities at an 18% add-on, with costs deducted from future profit sharing or a one-time lump sum payment option.
Independent valuation estimates Xdivane’s 10-year accumulated profit sharing at nearly SEK 10 billion, with a net present value of SEK 4.4 billion for the first four years or €408 million in January 2029 at a 15% discount rate.
Financial highlights
Q1 2026 revenue was SEK 17.3 million, with SEK 17.2 million from Ximluci product sales to STADA and a gross margin of 39%.
Profit sharing from STADA contributed SEK 13 million in Q1 2026, related to Q4 2025.
Operating cash flow for Q1 2026 was SEK -8.5 million; closing cash balance was SEK 66.7 million at quarter-end.
Administration expenses were SEK 7.6–17.6 million; R&D expenses were SEK 9.9 million, including SEK 2.7 million in amortization of intangibles.
EBITDA for Q1 2026 was SEK -7.8 million, with an equity ratio of 82%.
Outlook and guidance
Production cost reduction measures for Ximluci are expected to yield results from 2027 onwards, potentially unlocking further volume growth.
Regulatory decision on Ximluci’s U.S. BLA resubmission is expected within six months, with hopes for approval in H2/November 2026.
Xdivane’s clinical trial and CMC activities are on track, with anticipated U.S. launch in early 2029, pending timely approval.
Management expects existing financial resources to be sufficient for ongoing operations, assuming development proceeds as planned.
- Ximluci grew 63% in sales, held 8% market share, and net profit surged on asset divestment.XBRANE
Q4 202520 Feb 2026 - Ximluci sales surged and a US deal closed, but Biogen's exit makes out-licensing critical.XBRANE
Q2 202423 Jan 2026 - Q3 revenue up, Ximluci volumes rose 23%, urgent licensing deals needed for liquidity.XBRANE
Q3 202418 Jan 2026 - Biosimilars portfolio expands globally with cost efficiency, strong partnerships, and financial improvement.XBRANE
Investing in Life Science 202529 Dec 2025 - Ximluci sales soared, margins improved, and a key Xdivane partnership boosted outlook.XBRANE
Q4 202424 Dec 2025 - Financial turnaround with asset sale, share issue, and Ximluci's 11% growth in Europe.XBRANE
Q2 202523 Nov 2025 - Q1 profit turnaround and Alvotech deal enable focus on Ximluci and Xdivane.XBRANE
Q1 202517 Nov 2025 - Ximluci held 8% in Europe, Xdivane trials began, liquidity up, US launch delayed.XBRANE
Q3 202524 Oct 2025 - Xbrane is set for profitability from 2026, driven by derisked biosimilar assets and reduced costs.XBRANE
Company Presentation16 Jun 2025
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