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LCTXNYSE

Lineage Cell Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Phase 1·Carlsbad, CA, United States·CEO: Mr. Brian M. Culley M.A., M.B.A.
OncologyNeurologyOphthalmology

LCTX evidence brief

What we can confirm

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The company data is ready for cross-source review; unsupported conclusions remain unknown.

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Prepared research question

What matters most for LCTX—catalysts, financial risk and supporting evidence?

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BioSniper AI · LCTX

Lineage Cell Therapeutics is a clinical-stage biotechnology company developing allogeneic cell therapies for degenerative diseases, spinal cord injury, and other conditions, with a focus on its pluripotent cell manufacturing platform and a key collaboration with Roche/Genentech.

Key risk: Dependence on Roche collaboration

6.4/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$280.7M

Cash Runway

21.2 mo

Lead Asset

opc1 (Phase 1)

Next Catalyst

Financial data as of Jun 30, 2026.

Tracking 4 pipeline candidates · 1 clinical trial for Lineage Cell Therapeutics, Inc..

AI OverviewAI overview is shown in English only.

Lineage Cell Therapeutics is a clinical-stage biotechnology company developing allogeneic cell therapies for degenerative diseases, spinal cord injury, and other conditions, with a focus on its pluripotent cell manufacturing platform and a key collaboration with Roche/Genentech.

  • Lineage has successfully completed a cGMP production run from its two-tiered cell banking system for two product candidates, demonstrating scalable pluripotent cell manufacturing [sec_mda · as of 2026-03-05].
  • The company reported cash & equivalents of $37.9M, total revenue of $0.9M, net income of $1.5M, and no debt as of 2026-06-30 [sec].
  • Lineage is dependent on a third-party collaboration with Roche and Genentech to develop and commercialize RG6501 (OpRegen) [sec_mda · as of 2026-03-05].
  • As of June 30, 2026, $55.4 million remained available for sale under the company's at-the-market offering program [sec_mda · as of 2026-08-06].
  • A Phase 1 trial for delivery of oligodendrocyte progenitor cells for spinal cord injury began in June 2025 (NCT06841770) [catalyst].

What works

  • Lineage has demonstrated the ability to scale pluripotent cells with the purity, potency, and regulatory quality required for clinical use, which it believes is a competitive differentiator [sec_mda · as of 2026-03-05].
  • The company has a collaboration with Roche and Genentech, which provides potential for developmental, regulatory, and commercialization milestone and royalty payments [sec_mda · as of 2026-03-05].
  • Lineage has access to additional capital through up to $30.2 million in potential warrant exercises from the November 2024 RDO and an at-the-market offering program with $55.4 million remaining as of June 30, 2026 [sec_mda · as of 2026-08-06].

What to weigh

  • Lineage is dependent on its third-party collaboration with Roche and Genentech to develop and commercialize RG6501 (OpRegen), which introduces risks related to lack of control over those parties [sec_mda · as of 2026-03-05].
  • The company may need to raise additional capital to fund operations, and if unable to do so, may be required to delay, postpone, or cancel clinical trials [sec_mda · as of 2026-08-06].
  • The market price of Lineage's common shares has been and may continue to be volatile, and the company faces risks related to maintaining NYSE American listing standards [sec_mda · as of 2026-03-05].
  • A significant shareholder, affiliated with a board member, owns a large percentage of common shares and can exert substantial influence over corporate actions, including change of control transactions [sec_mda · as of 2026-03-05].

From the filings

Quoted directly from source documents.

  • Lineage has demonstrated scalable pluripotent cell manufacturing for clinical use.

    we have successfully completed a current cGMP production run from our two-tiered cell banking system for two of our product candidates. In at least one instance, they have been utilized in a U.S. Food and Drug Administration (FDA) cleared clinical trial in 2025. This demonstrates our ability to scale pluripotent cells with the purity, potency, and regulatory quality required for clinical use

    SEC MD&A · March 5, 2026

  • Lineage is dependent on a collaboration with Roche and Genentech for RG6501 (OpRegen).

    We are dependent on our third-party collaboration with F. Hoffmann-La Roche Ltd and Genentech, Inc to develop and commercialize RG6501 (OpRegen)

    SEC MD&A · March 5, 2026

  • Lineage has access to additional capital through warrant exercises and an at-the-market offering.

    We may receive up to an additional $30.2 million in gross proceeds upon the full cash exercise of the warrants we issued to the investors in the November 2024 RDO. However, no assurances can be given as to the extent to which additional warrants will be exercised. As of June 30, 2026, $55.4 million remained available for sale under our at-the-market offering program.

    SEC MD&A · August 6, 2026

  • Lineage's largest shareholder can exert substantial influence over the company.

    Our largest shareholder, who is affiliated with a member of our board of directors, owns a significant percentage of our common shares and will be able to exert substantial influence over the election of directors and matters subject to shareholder approval, including potential change of control transactions.

    SEC MD&A · March 5, 2026

Catalyst timeline

  • 2024-11-14 · Earnings Report - SEC 8-K filingQuarterly financial update and operational highlights.
  • 2025-03-10 · Earnings Report - SEC 8-K filingQuarterly financial update and operational highlights.
  • 2025-05-13 · Earnings Report - SEC 8-K filingQuarterly financial update and operational highlights.
  • 2025-06-30 · Phase 1 Start: Delivery of Oligodendrocyte Progenitor Cells for Spinal Cord InjuryInitiation of a Phase 1 trial evaluating a novel delivery device for cell therapy in spinal cord injury (NCT06841770).
  • 2025-08-12 · Earnings Report - SEC 8-K filingQuarterly financial update and operational highlights.
  • 2025-11-06 · Earnings Report - SEC 8-K filingQuarterly financial update and operational highlights.
Risks & what to watch (4)

Key risks

  • Dependence on Roche collaborationLineage relies on Roche/Genentech to develop and commercialize RG6501, with limited control over timelines and outcomes [sec_mda · as of 2026-03-05].
  • Need for additional capitalIf unable to raise capital, Lineage may delay or cancel clinical trials; warrant exercises and ATM offering provide potential but no guarantees [sec_mda · as of 2026-08-06].
  • Stock volatility and listing riskCommon shares have been volatile, and failure to maintain NYSE American listing could impair liquidity and capital raising [sec_mda · as of 2026-03-05].
  • Concentrated shareholder influenceA large shareholder affiliated with a board member can significantly influence director elections and major transactions [sec_mda · as of 2026-03-05].

What to watch

  • Progress of the Phase 1 trial for oligodendrocyte progenitor cells in spinal cord injury, which began recruiting in June 2025 (NCT06841770) [catalyst].
  • Any updates on the Roche/Genentech collaboration for RG6501 (OpRegen), including milestone or royalty payments [sec_mda · as of 2026-03-05].
  • Future capital raises, including potential warrant exercises (up to $30.2M) and use of the at-the-market offering program ($55.4M remaining as of June 30, 2026) [sec_mda · as of 2026-08-06].
  • Quarterly earnings reports and SEC filings for financial updates and clinical progress [catalyst].

Sources: Catalysts · SEC MD&A · Generated August 24, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash Runway5.9

21.2 months

Financial Health8.4

D/E 0.76 · 5% dilution

Pipeline Maturity4.0

Lead: Phase 1

Pipeline Breadth7.2

4 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal6.5

1 buy · 0 sells (180d)

Runway

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

131

Total value held

$189.0M

HolderSharesValue
broadwood capital inc49,560,992$78.3M
vanguard capital management llc16,637,370$26.3M
defender capital, llc.6,729,599$10.6M
millennium management llc5,561,374$8.8M
raffles associates lp5,362,788$8.5M
fifth third bancorp4,600,000$7.3M
blackrock, inc.3,864,757$6.1M
armistice capital, llc3,182,799$5.0M
marshall wace, llp3,065,033$4.8M
geode capital management, llc2,523,114$4.0M

Showing top 10 of 131 institutional holders of Lineage Cell Therapeutics, Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 20, 2026
% of float
17.1%
Days to cover
21.4
Shares short
25,474,080
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

LCTX short interest

Governance

Frequently asked questions

What is the AI investment thesis for Lineage Cell Therapeutics, Inc.?

Lineage Cell Therapeutics is a clinical-stage biotechnology company developing allogeneic cell therapies for degenerative diseases, spinal cord injury, and other conditions, with a focus on its pluripotent cell manufacturing platform and a key collaboration with Roche/Genentech.

What is Lineage Cell Therapeutics, Inc.'s lead drug candidate?

Lineage Cell Therapeutics, Inc.'s most advanced tracked candidate is opc1 (Phase 1) for Spinal Cord Injury Cervical.

Who is the CEO of Lineage Cell Therapeutics, Inc.?

Mr. Brian M. Culley M.A., M.B.A. is the chief executive officer of Lineage Cell Therapeutics, Inc. (LCTX).

Where is Lineage Cell Therapeutics, Inc. headquartered?

Lineage Cell Therapeutics, Inc. (LCTX) is headquartered in Carlsbad, CA, United States.

What therapeutic areas does Lineage Cell Therapeutics, Inc. focus on?

Lineage Cell Therapeutics, Inc. develops therapies across Oncology, Neurology, Ophthalmology.

925 companies232,681 SEC filings21,417 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.