Logotype for Lineage Cell Therapeutics Inc

Lineage Cell Therapeutics (LCTX) Q2 2026 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Lineage Cell Therapeutics Inc

Q2 2026 earnings summary

6 Aug, 2026

Executive summary

  • Advanced cell therapy pipeline leveraging the AlloSCOPE platform, with OpRegen as the lead asset in Phase 2a for geographic atrophy under Roche/Genentech partnership, and rapid progress in COR1, ILT1, and ReSonance/ANP1 programs.

  • OpRegen program continues with positive 3-year Phase 1/2a data, ongoing surgical optimization, expanded clinical trial sites (17), and EMA IRIS registration.

  • COR1 (corneal endothelial cell therapy) advanced to in-vivo animal testing, targeting Fuchs Endothelial Corneal Dystrophy and Bullous Keratopathy, with initial preclinical data expected in 2026.

  • OPC1 program shifted focus to chronic spinal cord injury patients, with ongoing DOSED study and positive safety profile.

  • ReSonance/ANP1 (auditory neuronal cell therapy) advancing in preclinical development with Demant partnership funding and successful GMP run.

Financial highlights

  • Cash, cash equivalents, and marketable securities totaled $50.8 million as of June 30, 2026, expected to fund operations into Q3 2028.

  • Q2 2026 revenue was $1.1 million, down from $2.8 million year-over-year, mainly due to lower collaboration and royalty revenues.

  • Operating expenses decreased to $10 million from $22.5 million year-over-year, reflecting the absence of a prior year $14.8 million impairment charge.

  • Net income for Q2 2026 was $1.5 million, or $0.01 per basic share, compared to a net loss of $30.5 million in Q2 2025, driven by non-cash gain from warrant liability remeasurement.

  • R&D expenses increased to $4.8 million and G&A expenses to $5.2 million in Q2 2026.

Outlook and guidance

  • Cash runway projected to support operations into Q3 2028.

  • Anticipates further updates on diabetes (ILT1) and COR1 programs before year-end, with initial COR1 preclinical data expected in 2026.

  • Ongoing enrollment in DOSED study for OPC1, with focus on chronic SCI patients and potential protocol adjustments.

  • Continued expectation for OpRegen to advance into a multi-center controlled trial.

  • Management anticipates continued operating losses and the need for additional capital to support future growth.

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