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Xilio Therapeutics (XLO) Q1 2025 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Xilio Therapeutics Inc

Q1 2025 earnings summary

14 Jan, 2026

Executive summary

  • Entered a major collaboration, license, and option agreement with AbbVie for up to four tumor-activated immunotherapy programs, including a $42M upfront payment and $10M equity investment, with up to $2.1B in potential milestones and royalties.

  • Reported $2.9M in collaboration and license revenue for Q1 2025, driven by new AbbVie and Gilead agreements; no product sales revenue.

  • Net loss for Q1 2025 was $13.3M, an improvement from $17.2M net loss in Q1 2024, reflecting lower R&D expenses and new collaboration revenue.

  • Cash and cash equivalents were $89.1M as of March 31, 2025, expected to fund operations into Q1 2026, but not for 12 months from report issuance, raising substantial doubt about going concern.

  • Presented initial Phase 2 data for vilastobart in combination with atezolizumab, showing a 27% objective response rate in late-line MSS CRC patients without liver metastases and a favorable safety profile.

Financial highlights

  • Q1 2025 revenue: $2.9M (vs. $0 in Q1 2024), all from collaboration and license agreements.

  • Net loss: $13.3M in Q1 2025 (vs. $17.2M in Q1 2024); net loss per share improved to $(0.18) from $(0.62) year-over-year.

  • R&D expenses decreased to $8.3M (from $10.4M), mainly due to portfolio reprioritization and lower headcount.

  • G&A expenses increased to $8.5M (from $6.1M), driven by higher personnel and professional fees.

  • Cash provided by operating activities was $29.0M in Q1 2025, reflecting upfront payments from AbbVie.

Outlook and guidance

  • Cash runway expected into Q1 2026, but not sufficient for 12 months from financial statement issuance; additional capital needed to continue operations.

  • Management is pursuing additional equity, debt, or partnership funding; failure to secure capital may require cost reductions or program delays.

  • Plans to report updated Phase 2 data for vilastobart at ASCO 2025 and nominate development candidates for multiple T cell engager programs in 2025 and 2026.

  • No product sales expected for several years; future revenue to depend on milestone payments and royalties from AbbVie and Gilead collaborations.

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