Logotype for Immunocore Holdings plc

Immunocore (IMCR) Q2 2025 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Immunocore Holdings plc

Q2 2025 earnings summary

25 Feb, 2026

Executive summary

  • KIMMTRAK net sales reached $192 million in H1 2025, up 32% year-over-year, with approvals in 39 countries and launches in 28, maintaining standard of care status in HLA-A*02:01-positive metastatic uveal melanoma and 68% market penetration.

  • Robust pipeline progress with three Phase III registrational trials in oncology (TEBE-AM, ATOM, PRISM-MEL-301), expansion into autoimmunity and infectious diseases, and a type 1 diabetes program set to start clinical trials in 2026.

  • Cash and marketable securities totaled $883 million as of June 30, 2025, supporting continued R&D and commercial activities.

  • Net loss for H1 2025 narrowed to $5.3 million from $36 million in the prior year, reflecting revenue growth outpacing operating expenses.

  • SG&A and R&D expenses increased, with R&D up 35% year-over-year in Q2 2025, reflecting pipeline advancement.

Financial highlights

  • Q2 2025 net sales were $98 million, up 30% year-over-year, with H1 2025 net sales at $191.8 million, up 32% year-over-year.

  • US Q2 2025 revenue was $64.1 million (up 15% year-over-year); Europe was $33 million (up 115% year-over-year), driven by launches and price agreements.

  • Net loss for Q2 2025 was $10.3 million, with basic and diluted net loss per share at $(0.20); H1 2025 net loss per share was $(0.11).

  • SG&A expenses averaged $42 million per quarter and are expected to remain flat for the rest of 2025.

  • Cash and marketable securities increased to $883 million from $820.4 million at year-end 2024.

Outlook and guidance

  • KIMMTRAK is expected to continue growing at a moderate rate as the product matures, with further expansion in new geographies and indications.

  • R&D expenses will increase as investments in three Phase III trials and early-stage programs continue.

  • TEBE-AM Phase III trial enrollment expected to complete within 12 months, with data readout possible in H2 2026.

  • Dose selection for PRISM-MEL-301 Phase III trial anticipated in H2 2025; ATOM trial site activation ongoing.

  • Approximately $65 million in sales-related rebate accruals expected to be paid in H2 2025.

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