| Metric | Value ($ M) | Q2 FY26 | Q3 FY25 |
|---|---|---|---|
| Revenue | 1.43 | 33.6% | 61.1% |
| Total Income | 1.43 | 33.6% | 61.1% |
| Expenditure | 8.75 | 12.4% | 17.1% |
| PBT | 4.71 | ||
| Net Profit | 4.23 | 185.8% | 114.2% |
| OPM | — | ||
| NPM | 100.00% | 0.00pp | |
| EPS | 0.02 | 100.0% | 115.4% |
Lineage Cell Therapeutics Reports Q3 2026 Results and Business Update
13 Nov 2026 · 4h ago
Summary
Lineage Cell Therapeutics reported its third quarter 2026 financial and operating results, highlighted by the acquisition of NeuroAirmid Therapeutics and its HUNT1 program for Huntington's Disease. The company also advanced its proprietary manufacturing technology with a new patent for its AlloSCOPE™ “5D” Technology. Financial results showed total revenues of approximately $1.5 million for the three months ended September 30, 2026, a decrease compared to the prior year, while operating expenses increased to $8.8 million. The company reported a net income of $4.2 million for the quarter, a significant improvement from the net loss in the same period of 2025, largely due to non-cash fair value remeasurement of warrant liabilities. Management expressed focus on building a diversified portfolio and leveraging its manufacturing expertise.
Key Highlights
- 1
Lineage Cell Therapeutics acquired NeuroAirmid Therapeutics, Inc., adding HUNT1, a third clinical-stage asset for Huntington's Disease, to its development pipeline.
- 2
The company announced the issuance of a patent covering its AlloSCOPE™ “5D” Technology, a key component of its cell manufacturing platform.
- 3
The collaboration with William Demant Invest for ReSonance® advanced into its second year, with a Danish Medicines Agency meeting scheduled for Q4 2026.
- 4
Lineage Cell Therapeutics' Corneal Endothelial Disease Program (COR1) has advanced into preclinical testing, with initial data expected in Q1 2027.
- 5
OpRegen® Cell Therapy continues to be evaluated in Genentech’s GAlette Study for the treatment of Dry-AMD with Geographic Atrophy.
- 6
Cash, cash equivalents, and marketable securities as of September 30, 2026, are expected to support planned operations into Q2 2028.
Management Comments
Brian M. Culley
While our collaboration with Roche and Genentech for the development of the OpRegen cell therapy program for dry AMD with geographic atrophy continues to advance, we are focused on using our platform to build a diversified portfolio of additional allogeneic cell transplant programs. Today, we closed the acquisition of NeuroAirmid Therapeutics adding HUNT1, a third clinical-stage asset to our development pipeline. HUNT1 is a pluripotent stem cell derived, clinical-stage neural cell therapy program, with the potential to validate a new cell-based treatment modality for Huntington’s Disease. When we evaluated this opportunity, what stood out was the substantial development work that had been completed, external capital had been invested, and we believed our manufacturing expertise could create significant additional value for this program. This transaction reflects the disciplined approach to capital allocation and strategic fit that we believe our investors have come to expect from Lineage. HUNT1 was created on the same proprietary cell line that Lineage uses and is compatible with its AlloSCOPE “5D” technology, providing us with a head start on our planned contributions. Leveraging our experience with this line and our capabilities in cell manufacturing, process development, and scale-up, we intend to deploy our resources to migrate the HUNT1 process to our AlloSCOPE manufacturing platform and to support the evolution of HUNT1 onto a commercially viable and scalable production system more suitable to supporting late-stage registrational trials in parallel with its ongoing clinical development. In addition, the ongoing REGEN4HD clinical trial of HUNT1 is supported in part by a CIRM grant, reducing our out-of-pocket development costs. In addition to this exciting acquisition, we also strengthened our proprietary manufacturing position through the issuance of a U.S. patent covering our AlloSCOPE 5D technology. 5D is an approach which we believe may provide a differentiated solution to one of the most important challenges facing the allogeneic cell therapy industry: enabling commercially-scalable and consistent manufacturing of pluripotent cell-derived therapies. We recently deployed AlloSCOPE 5D to COR1, our wholly owned corneal endothelial cell therapy program, and expect initial preclinical data in the first quarter of 2027, demonstrating the speed, scalability, and versatility of our development platform. We also continued to employ 5D technology to advance our ILT1 program, which ultimately may become a treatment for Type 1 Diabetes. In parallel with supporting the development of the OpRegen cell therapy program through the production, release, and delivery of multiple GMP batches of clinical trial material, we are prioritizing other programs that we believe can generate meaningful data in early clinical trials, and which supports our plan to optimize capital allocation and accelerate value creation. By combining strategic business development, proprietary manufacturing technologies, and internally generated innovation, we believe we are building a differentiated pipeline and positioning Lineage to create sustainable long-term value for our shareholders.
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