Logotype for Lineage Cell Therapeutics Inc

Lineage Cell Therapeutics (LCTX) Q2 2024 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Lineage Cell Therapeutics Inc

Q2 2024 earnings summary

2 Feb, 2026

Executive summary

  • The company is a clinical-stage biotech focused on allogeneic cell therapies, with a proprietary platform and strategic collaborations, notably with Roche/Genentech for OpRegen in ocular disorders.

  • OpRegen, the lead partnered program, is in Phase II for geographic atrophy secondary to AMD, with new ex-U.S. clinical sites and positive 24-month visual acuity data; the Roche agreement includes up to $620 million in milestones and double-digit royalties.

  • Expanded partnership with Roche/Genentech includes a new service agreement, extended patient follow-up, and manufacturing support, fully funded by Genentech.

  • Pipeline includes OPC1 for spinal cord injury (preparing for a new clinical study pending FDA feedback) and ANP1 for hearing loss, plus a gene editing collaboration with Eterna.

  • Operations and manufacturing are concentrated in Israel, with business continuity plans in place due to risks from the Israel-Hamas war.

Financial highlights

  • Cash, cash equivalents, and marketable securities totaled $38.5 million as of June 30, 2024, supporting operations into Q4 2025.

  • Q2 2024 revenues were $1.4 million, down 56% year-over-year, mainly due to lower collaboration/licensing revenue.

  • Operating expenses for Q2 2024 were $7.3 million, down 12% year-over-year, with R&D expenses at $2.9 million and G&A at $4.3–4.4 million.

  • Net loss for Q2 2024 was $5.8 million ($0.03/share), compared to $5.2 million ($0.03/share) in Q2 2023.

  • Cash used in operating activities for H1 2024 was $11.0 million, improved from $17.5 million in the prior year; net cash from financing was $14.1 million.

Outlook and guidance

  • Cash runway extends into Q4 2025, not including potential milestone payments from Roche.

  • Management expects current resources to fund operations for at least twelve months from the financial statement date.

  • Awaiting FDA clearance to initiate OPC1 dose study and apply for a CIRM grant, which could offset up to half of trial costs.

  • Updates expected soon on OpRegen data, OPC1 clinical progress, and ANP1 preclinical results.

  • The company anticipates continued operating losses and will require significant additional capital for future development and regulatory activities.

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