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CLCSOTC

Cell Source, Inc.

Biopharma developer (SEC filing verified)·Phase 1·New York, NY, United States·CEO: Mr. Itamar Shimrat
Oncology

CLCS evidence brief

What we can confirm

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What it means

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

What to watch

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Prepared research question

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

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BioSniper AI · CLCS

Cell Source, Inc. (CLCS) is a biotechnology company developing cell therapy treatments based on immune tolerance management, currently facing significant financial uncertainty with no revenue and a going concern warning.

Key risk: Going concern uncertainty

2.0/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$39.3M

Cash Runway

0.0 mo

Lead Asset

Veto Cell (Phase 1)

Next Catalyst

Financial data as of Mar 31, 2025.

Tracking 1 pipeline candidate for Cell Source, Inc..

AI OverviewAI overview is shown in English only.

Cell Source, Inc. (CLCS) is a biotechnology company developing cell therapy treatments based on immune tolerance management, currently facing significant financial uncertainty with no revenue and a going concern warning.

  • Cell Source is a biotechnology company focused on developing cell therapy treatments based on the management of immune tolerance [sec_mda · as of 2018-11-14].
  • As of March 31, 2025, the company reported cash of $0.0M, net income of -$1.5M, and shareholders' equity of -$15.6M [sec].
  • The company has not generated any revenues and has a working capital deficiency; as of June 30, 2024, the working capital deficiency was approximately $17.3 million [sec_mda · as of 2024-08-19].
  • Management's plans include continued efforts to raise additional capital through debt and equity financings, but there is no assurance these funds will be sufficient [sec_mda · as of 2026-05-14].
  • The company's Veto Cell clinical trial has shown no toxicity, with patients showing successful stem cell engraftment in the absence of severe GvHD [sec_mda · as of 2024-08-19].

What works

  • The Veto Cell clinical trial has demonstrated no toxicity and successful stem cell engraftment without severe GvHD, indicating potential for a differentiated cell therapy [sec_mda · as of 2024-08-19].
  • The company has a technology platform extensively tested by in vitro studies and confirmed in animal trials, providing a scientific foundation [sec_mda · as of 2018-11-14].

What to weigh

  • The company has no revenue, a negative shareholders' equity of -$15.6M as of March 31, 2025, and a working capital deficiency of $17.3M as of June 30, 2024, indicating severe financial distress [sec] [sec_mda · as of 2024-08-19].
  • There is substantial doubt about the company's ability to continue as a going concern for at least one year, and operations are funded on a month-to-month basis [sec_mda · as of 2024-07-29].
  • Notes payable with principal amounts totaling $5,643,000 and $1,956,000 were past due as of 2024 and through the date of filing, highlighting liquidity pressure [sec_mda · as of 2024-07-29].
  • Management acknowledges that if additional financing is not obtained, the company may have to curtail development and could be forced to discontinue operations [sec_mda · as of 2026-05-14].

From the filings

Quoted directly from source documents.

  • There is substantial doubt about the company's ability to continue as a going concern.

    These conditions raise substantial doubt about our ability to continue as a going concern for at least one year from the date these financial statements are issued.

    SEC MD&A · July 29, 2024

  • The Veto Cell trial has shown no toxicity and successful engraftment.

    This trial has thus far shown that there has been no toxicity associated with the Veto Cells, with patients consistently showing successful stem cell engraftment, in the absence of severe GvHD.

    SEC MD&A · August 19, 2024

  • Management plans to raise additional capital but there is no assurance of success.

    Management's plans include continued efforts to raise additional capital through debt and equity financings. There is no assurance that these funds will be sufficient to enable us to fully complete our development activities or attain profitable operations.

    SEC MD&A · May 14, 2026

Risks & what to watch (3)

Key risks

  • Going concern uncertaintySubstantial doubt about ability to continue as a going concern; operations funded month-to-month [sec_mda · as of 2024-07-29].
  • Liquidity and capital needsNo revenue, negative equity, and past due notes; reliant on uncertain future financings [sec] [sec_mda · as of 2024-07-29].
  • Clinical and regulatory riskVeto Cell trial is ongoing; no approved products; failure could halt development [sec_mda · as of 2024-08-19].

What to watch

  • Ability to secure additional debt or equity financing to continue operations [sec_mda · as of 2026-05-14].
  • Progress and results of the Veto Cell clinical trial, including future cohort data [sec_mda · as of 2024-08-19].
  • Resolution of past due notes payable and any conversion or extension agreements [sec_mda · as of 2024-07-29].

Sources: SEC MD&A · Generated August 28, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash Runway0.0

0.0 months

Financial Health0.5

OCF -$600K · Net income -$1M

Pipeline Maturity4.0

Lead: Phase 1

Pipeline Breadth3.3

1 candidate

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Financials

Frequently asked questions

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

Cell Source, Inc. (CLCS) is a biotechnology company developing cell therapy treatments based on immune tolerance management, currently facing significant financial uncertainty with no revenue and a going concern warning.

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

Cell Source, Inc.'s most advanced tracked candidate is Veto Cell (Phase 1) for Allogeneic hematopoietic stem cell transplantation (HSCT).

Who is the CEO of Cell Source, Inc.?

Mr. Itamar Shimrat is the chief executive officer of Cell Source, Inc. (CLCS).

Where is Cell Source, Inc. headquartered?

Cell Source, Inc. (CLCS) is headquartered in New York, NY, United States.

What therapeutic areas does Cell Source, Inc. focus on?

Cell Source, Inc. develops therapies across Oncology.

925 companies232,681 SEC filings21,419 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.