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AbCellera Biologics (ABCL) Q2 2024 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for AbCellera Biologics Inc

Q2 2024 earnings summary

2 Feb, 2026

Executive summary

  • Capital allocation prioritized internal pipeline advancement, platform and facility investments, and select strategic partnerships, including expanded collaborations with Eli Lilly, Regeneron, and Gilead.

  • Internal pipeline programs ABCL-635 and ABCL-575 are progressing toward clinical trial applications in Q2 2025.

  • Four T-cell engager molecules are advancing into preclinical efficacy models, targeting oncology and autoimmunity.

  • Achieved partner milestones: Abdera's ABD-147 received IND clearance and FDA Fast Track; Invetx to be acquired by Dechra Pharmaceuticals for up to $520 million, with equity and royalty stakes held.

  • Two internal programs advanced into IND-enabling studies this quarter.

Financial highlights

  • Q2 2024 revenue was $7.3 million, down from $10.1 million in Q2 2023, mainly due to lower research fees and $1.5 million in milestone payments.

  • Net loss for Q2 2024 was $36.9 million ($0.13 per share), compared to $30.5 million ($0.11 per share) in Q2 2023.

  • Operating expenses rose to $100.8 million in Q2 2024, up from $61.4 million in Q2 2023, driven by a $32 million impairment charge related to the TetraGenetics acquisition.

  • R&D expenses increased to $40.9 million; G&A expenses rose to $20.2 million.

  • Cash, cash equivalents, and marketable securities totaled $697.6 million as of June 30, 2024, with over $900 million in total available liquidity including government funding.

Outlook and guidance

  • ABCL-635 and ABCL-575 expected to submit clinical trial applications in Q2 2025.

  • Research fee revenue expected to trend lower as focus shifts to internal and co-development programs.

  • Continued significant investment in R&D, internal pipeline, and infrastructure, with no need for additional external funding anticipated for at least the next 36 months.

  • Investments in CMC and GMP manufacturing capabilities to continue at current rate through 2024, substantially complete by early 2025.

  • Revenue expected to remain variable and dependent on partner milestones and out-licensing success.

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