SNTINasdaqBiological Products, (No Diagnostic Substances)US GAAP · USD

Senti Biosciences Holdings, Inc.

Senti Biosciences Holdings, Inc. is a U.S.-based biotechnology company developing engineered cell and gene therapies built around synthetic biology and gene-circuit design. Its work centers on preclinical and clinical-stage product candidates, with development activities, manufacturing coordination, and collaboration arrangements conducted through its corporate and subsidiary structure.

Revenue0.0m USD
Operating profit (EBIT)-68.8m USD
−12.7 %y/y
EBIT margin-312,631.8%
Net income-61.4m USD
−16.4 %y/y
Free cash flow-43.6m USD
−5.4 %y/y

Fiscal year 2025 · change from previous year

Development 2021–2025

-100-80-60-40-20020m USD2021: 2.8 m USD2021: EBIT -40 m USD20212022: 4.3 m USD2022: EBIT -62 m USD20222023: 2.6 m USD2023: EBIT -93 m USD20232024: 0.00 m USD2024: EBIT -61 m USD20242025: 0.02 m USD2025: EBIT -69 m USD20250.02-69
RevenueOperating profit (EBIT)

Business

Share of revenue
Cell therapy product candidates40 %

Engineered therapeutic candidates designed to target disease through modified cells.

Gene-circuit platforms25 %

Synthetic biology platforms used to design programmable therapeutic behavior.

Collaboration revenue10 %

Fees and milestone-like payments from research or option agreements with partners.

Preclinical and translational research15 %

Discovery and early-stage development work supporting future product candidates.

Manufacturing and process development10 %

Development and scale-up activities needed to produce clinical-grade material.

Customers

Senti’s direct customers are primarily collaboration partners, research counterparties, and future commercial buyers of approved therapies rather than end-market patients today. The company’s current economic model depends on licensing, option agreements, and development partnerships while its product candidates move through clinical testing and manufacturing scale-up.

Biopharmaceutical collaboration partners

Partners license, option, or co-develop Senti's synthetic biology and cell therapy programs.

Research and development counterparties

Organizations that pay for access to programs, data, or development rights during early-stage work.

Clinical trial ecosystem

Hospitals, investigators, and trial operators that support testing of product candidates.

Future commercial healthcare providers

Oncology treatment centers and hospitals that would use approved therapies if launched.

Strategy

Senti’s strategy is to concentrate resources on a small number of lead programs while using partnerships to extend the reach of its platform technology. The company also relies on external manufacturing and collaboration structures to advance clinical development without building a full commercial infrastructure before approval.

Advance SENTI-202 through clinical and manufacturing milestonesShort term

The lead program is central to validating the platform and creating future value.

Partner non-core programs and gene-circuit applicationsMedium term

Partnerships can fund development and broaden the platform without full internal spend.

Maintain flexible operating structureMedium term

A lean structure reduces the need to build commercial and manufacturing infrastructure too early.

Geography

Senti is headquartered in the United States and conducts its core research, development, and corporate activities there. The company also references international collaboration and partnership exposure, including a stated focus on partnership activity in China for one program, which adds regulatory and execution complexity outside the U.S.

Risks

Senti is an early-stage biotechnology company with no approved products, so its value depends on successful clinical development, regulatory outcomes, and access to funding. The business also depends on third-party manufacturing and collaboration arrangements, which can create concentration, execution, and collectibility risk if partners underperform.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Clinical development failure1Financing and dilution risk2Manufacturing partner dependence3Collectibility and counterparty risk4International collaboration risk5
Impact is the risk’s severity and likelihood how probable it is over the next few years, both assessed from the company’s reports. Numbers match the list.
  1. Clinical development failureImpact: CriticalLikelihood: High

    Product candidates may not show sufficient safety or efficacy in trials.

    Exposure: Lead programs such as SENTI-202

  2. Financing and dilution riskImpact: HighLikelihood: High

    The company has no product sales and relies on external capital to fund operations.

    Exposure: Equity and convertible note financing

  3. Manufacturing partner dependenceImpact: HighLikelihood: High

    Clinical supply is reliant on GeneFab and other third parties for scale-up and continuity.

    Exposure: SENTI-202 manufacturing

  4. Collectibility and counterparty riskImpact: MediumLikelihood: High

    Related-party sublease and collaboration income depend on partner payments.

    Exposure: GeneFab sublease and BlueRock agreement

  5. International collaboration riskImpact: MediumLikelihood: Medium

    Cross-border partnerships can face regulatory, political, and operational friction.

    ExposureNon-U.S. partneringIncluding China-related activity
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Accounting

Judgemental items
Collaboration revenue recognition

Revenue from option exercise period extensions is recognized ratably over the period, affecting timing.

Impact: BlueRock-related collaboration revenue

Related-party sublease accounting

Sublease income can be reversed if collectibility is no longer probable under lease accounting rules.

Impact: GeneFab and headquarters sublease income

Fair value measurement of financing-related instruments

Convertible notes, options, and economic share arrangements may require remeasurement.

Impact: Reported other income/expense and balance sheet liabilities

Lease modification accounting

Lease changes can create one-time gains or losses that distort period comparability.

Impact: Operating results and lease-related line items

R&D expense classification

External services and supplies drive most development spend and can shift sharply quarter to quarter.

Impact: Comparability of research and development expense

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026