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AbCellera Biologics Inc.: Q4 FY2025 earnings call

What management said about Q4 FY2025, from the documents filed with the SEC on 24 February 2026: press release. The quarter’s numbers.

Key takeaways

  • Revenue rose on litigation settlement: Fourth quarter revenue was mainly an upfront patent litigation settlement payment. Full-year revenue was $75.1 million, up from $28.8 million in 2024. Source
  • Full-year net loss was smaller: Full-year net loss was $146.4 million, or $(0.49) per share, against $162.9 million, or $(0.55) per share, in 2024. Source
  • ABCL635 entered Phase 2: ABCL635 entered the Phase 2 portion of its Phase 1/2 trial at the end of 2025. The third quarter release had described it as progressing through Phase 1. Source
  • Two candidates moved toward IND: Two development candidates, ABCL688 and ABCL386, moved into IND/CTA-enabling activities during 2025. Source
  • Clinical manufacturing facility opened: Platform investments were completed during 2025, and the clinical manufacturing facility is now open. Source
  • Liquidity near $700 million: Year-end liquidity was about $700 million, combining total cash, cash equivalents and marketable securities with available non-dilutive government funding. Source

“In 2025, AbCellera successfully delivered on all its corporate priorities, transitioned to a clinical-stage biotech company, and ended the year with approximately $700 million in available liquidity to execute on our strategy”

Carl Hansen, Ph.D., founder and CEO of AbCellera

What changed from last quarter

  • New: ABCL635 entered the Phase 2 portion of its Phase 1/2 clinical trial at the end of 2025. The third quarter release described it as progressing through Phase 1. Source
  • New: The company completed its multi-year platform investments and opened its clinical manufacturing facility. The third quarter release said activities had started at the facility. Source
  • New: Fourth quarter revenue included an upfront settlement payment from the company's patent litigation. Source
  • New: Two development candidates, ABCL688 and ABCL386, moved into IND/CTA-enabling activities. Neither was named in the third quarter release. Source

Results and growth drivers

  • Revenue rose on litigation settlement: Fourth quarter revenue was mainly an upfront patent litigation settlement payment. Full-year revenue was $75.1 million, up from $28.8 million in 2024. Source
  • Full-year net loss was smaller: Full-year net loss was $146.4 million, or $(0.49) per share, against $162.9 million, or $(0.55) per share, in 2024. Source
  • Fourth quarter loss reported: The net loss for the fourth quarter was $8.9 million, or $(0.03) per share, on a basic and diluted basis. Source

Costs and operating expenses

  • Fourth quarter operating spend reported: Fourth quarter operating expenses were $73.4 million, including co-development and internal program investments, equal to 25% of full-year operating expenses. Source
  • Internal programs drove R&D mix: A larger share of R&D spending went to internal programs, including $21.0 million of specific investments in internal programs during 2025. Source
  • Sales and admin spend slightly lower: Sales, general and administrative expenses were slightly lower in 2025 than in 2024. Source
  • Amortization and impairment charge fell: Depreciation, amortization and impairment were $22,171 thousand in 2025, compared with $90,850 thousand in 2024. Total operating expenses were $292,231 thousand. Source

“We entered 2026 with a fully built platform, a growing pipeline with multiple potential first-in-class programs and important near-term clinical readouts, and sufficient liquidity to fund well beyond the next three years of pipeline investments.”

Carl Hansen, Ph.D., founder and CEO of AbCellera

Clinical pipeline and partner programs

  • ABCL635 entered Phase 2: ABCL635 entered the Phase 2 portion of its Phase 1/2 trial at the end of 2025. The third quarter release had described it as progressing through Phase 1. Source
  • ABCL575 still in Phase 1: ABCL575 remained in Phase 1 at year end. Source
  • Two candidates moved toward IND: Two development candidates, ABCL688 and ABCL386, moved into IND/CTA-enabling activities during 2025. Source
  • Partner molecule entered clinic in Q4: A partner advanced one molecule into the clinic during the fourth quarter. Source

Facilities and platform

  • Clinical manufacturing facility opened: Platform investments were completed during 2025, and the clinical manufacturing facility is now open. Source

Liquidity and capital

  • Liquidity near $700 million: Year-end liquidity was about $700 million, combining total cash, cash equivalents and marketable securities with available non-dilutive government funding. Source
  • Operating cash outflow widened: Net cash used in operating activities was $(131,295) thousand in 2025, against $(108,556) thousand in 2024. Source
  • Equipment purchases declined: Purchases of property and equipment were $(42,772) thousand in 2025, against $(78,396) thousand in 2024. Source

People and leadership

  • Chief Medical Officer appointed: Sarah Noonberg, M.D., Ph.D., was appointed Chief Medical Officer, expanding the leadership team. The third quarter release had already reported this appointment. Source

Strategy and company direction

  • Shift to clinical-stage company: Management said the company transitioned to a clinical-stage biotech company during 2025. Source

Figures management reported

FigureReported
Molecules in the clinic (cumulative) Source19
Partner-initiated program starts with downstreams (cumulative) Source104
Research and development expenses Source$186.8 million

Earlier plans management reported on

  • Met: Management said the company successfully delivered on all of its 2025 corporate priorities. Source
  • Not stated: The third quarter release said the company would keep advancing its two lead programs through Phase 1. The year-end release reports ABCL635 in Phase 2.

Other quarters

Summarised with AI from the documents the company filed with the SEC. Every point is checked against the filing before it is shown: management’s own words word for word, figures against the line or table row they come from. A point that fails the check is left out. Source opens the filing at that line.