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Senti Bio Reports Fourth Quarter and Full Year 2025 Financial Results and Provides a Corporate Update

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Senti Biosciences (Nasdaq: SNTI) reported fourth-quarter and full-year 2025 results and a corporate update on March 27, 2026. Key highlights: RMAT designation for SENTI-202 in relapsed/refractory AML, updated positive preliminary Phase 1 data for SENTI-202, and continued Gene Circuit platform progress.

Financials: $16.4M cash at Dec 31, 2025; Q4 R&D $7.8M; FY2025 R&D $37.6M; Q4 G&A $5.8M; FY2025 G&A $26.2M; Q4 net loss $14.5M ($0.53/share); FY net loss $61.4M ($2.73/share) including a $5.1M impairment and $5.7M stock‑based comp.

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Positive

  • Received RMAT designation for SENTI-202 from FDA
  • Reported positive preliminary Phase 1 SENTI-202 clinical data (encouraging responses and safety)
  • Maintained platform progress across Gene Circuit–engineered cell therapy programs

Negative

  • Low liquidity: $16.4M cash at December 31, 2025
  • Full‑year net loss of $61.4M (includes $5.1M impairment)

Market Reaction – SNTI

+2.46% $0.81 2.1x vol
15m delay 14 alerts
+2.46% Since News
$0.81 Last Price
$0.79 $0.86 Day Range
+$499K Valuation Impact
$20.77M Market Cap
2.1x Rel. Volume

Following this news, SNTI has gained 2.46%, reflecting a moderate positive market reaction. Our momentum scanner has triggered 14 alerts so far, indicating notable trading interest and price volatility. The stock is currently trading at $0.81. This price movement has added approximately $499K to the company's valuation. Trading volume is elevated at 2.1x the average, suggesting notable buying interest.

Data tracked by StockTitan Argus (15 min delayed). Upgrade to Silver for real-time data.

Key Figures

Cash & equivalents: $16.4 million R&D expenses: $37.6 million G&A expenses: $26.2 million +5 more
8 metrics
Cash & equivalents $16.4 million As of December 31, 2025
R&D expenses $37.6 million Full year 2025
G&A expenses $26.2 million Full year 2025
Net loss (Q4 2025) $14.5 million Three months ended December 31, 2025
EPS (Q4 2025) $0.53 loss per share Basic and diluted, quarter ended December 31, 2025
Net loss (FY 2025) $61.4 million Year ended December 31, 2025
EPS (FY 2025) $2.73 loss per share Full year 2025
Asset impairment $5.1 million Non-recurring impairment of long-lived assets in 2025 net loss

Market Reality Check

Price: $0.8814 Vol: Volume 48,663 is below 20...
low vol
$0.8814 Last Close
Volume Volume 48,663 is below 20-day average 108,075 (relative volume 0.45x). low
Technical Price 0.8814 trades below 200-day MA 1.55 and 82.72% under 52-week high 5.10.

Peers on Argus

SNTI was modestly up (0.03%) while only one peer in momentum (RANI) moved -1.85%...
1 Down

SNTI was modestly up (0.03%) while only one peer in momentum (RANI) moved -1.85% without news, indicating stock-specific trading rather than a coordinated biotech move.

Previous Earnings Reports

4 past events · Latest: Mar 20 (Positive)
Same Type Pattern 4 events
Date Event Sentiment Move Catalyst
Mar 20 Annual results 2024 Positive +4.8% Reported 2024 results, strong SENTI-202 data, PIPE financing and higher cash.
Nov 14 Q3 2024 earnings Positive -7.7% Q3 2024 results with lower expenses but modest cash and ongoing trial spend.
Aug 13 Q2 2024 earnings Positive +10.2% Q2 2024 results plus CIRM grant and SENTI-301A pilot trial plans.
May 09 Q1 2024 earnings Positive -0.3% Q1 2024 results with SENTI-202/301A progress and ongoing operating losses.
Pattern Detected

Earnings releases have generally been viewed positively but with mixed price follow-through: two positive and two negative next-day moves, despite broadly constructive operational updates.

Recent Company History

Across the last four earnings-related updates from May 2024 through March 2025, Senti Bio repeatedly paired financial reporting with SENTI-202 clinical progress and balance sheet actions. Prior reports highlighted PIPE financing, CIRM grants, and cash levels between $10.5M and $48.3M, alongside sizeable net losses. Price reactions ranged from a -7.73% decline to a 10.15% gain, showing no consistent trend. Today’s 2025 results continue this pattern of significant R&D spend and pipeline updates against a constrained cash position.

Historical Comparison

+1.7% avg move · Past earnings and annual result releases for SNTI moved the stock an average of 1.74%. Today’s earni...
earnings
+1.7%
Average Historical Move earnings

Past earnings and annual result releases for SNTI moved the stock an average of 1.74%. Today’s earnings-linked move of 0.03% sits at the low end of that historical range.

Earnings updates have tracked SENTI-202’s evolution from early Phase 1 data to deeper remissions, while also detailing cash fluctuations, PIPE financing, CIRM grants, and expense controls.

Market Pulse Summary

This announcement combines 2025 financial results with updates on SENTI-202’s Phase 1 data and RMAT ...
Analysis

This announcement combines 2025 financial results with updates on SENTI-202’s Phase 1 data and RMAT status, set against year‑end cash of $16.4M and a full‑year net loss of $61.4M. Historical earnings releases have mixed price impacts but consistently emphasize pipeline progress and balance‑sheet constraints. Investors may focus on the pace of clinical development for SENTI‑202, expense trends in R&D and G&A, and any future financing actions or lease restructurings disclosed in recent SEC filings when assessing ongoing risk.

Key Terms

phase 1, relapsed/refractory acute myeloid leukemia, regenerative medicine advanced therapy (rmat) designation, u.s. food and drug administration
4 terms
phase 1 medical
"Reported updated positive preliminary clinical data from the ongoing Phase 1 trial of SENTI-202"
Phase 1 is the first stage of testing a new drug or medical treatment in people, focused primarily on safety, how the body handles the product, and finding a tolerated dose. Think of it as a short, tightly controlled experiment with a small group to check for dangerous side effects before wider testing; for investors it is an early milestone that reduces some uncertainty but still carries high risk and potential for both big value changes and setbacks.
relapsed/refractory acute myeloid leukemia medical
"Phase 1 trial of SENTI-202 in relapsed/refractory acute myeloid leukemia (AML)"
A form of acute myeloid leukemia (AML) that either returns after an initial response to treatment (relapsed) or fails to improve or continues progressing despite therapy (refractory). For investors, this describes a high unmet medical need and a patient group often targeted by new drugs, clinical trials and regulatory priority pathways, so developments here can meaningfully affect a company’s trial success prospects, market size and potential revenue.
regenerative medicine advanced therapy (rmat) designation regulatory
"Received Regenerative Medicine Advanced Therapy (RMAT) designation from the U.S. Food and Drug Administration"
A Regenerative Medicine Advanced Therapy (RMAT) designation is a U.S. regulatory status given to certain cell, gene, or tissue-based treatments that show promise for serious conditions and early clinical evidence of benefit. It signals that regulators will provide extra guidance and expedited review steps—like giving a promising project a “fast pass” through some development checkpoints—which can shorten time to market and reduce regulatory risk, making the program more valuable and noteworthy to investors.
u.s. food and drug administration regulatory
"Regenerative Medicine Advanced Therapy (RMAT) designation from the U.S. Food and Drug Administration for SENTI-202"
The U.S. Food and Drug Administration is the federal agency that evaluates and enforces safety, effectiveness and labeling standards for medicines, medical devices, vaccines, food and related products before they reach consumers. For investors it matters because FDA approvals, warnings or recalls determine whether a product can be sold, how quickly it reaches the market and how costly compliance will be—changes that directly affect a company’s revenue, costs and stock value.

AI-generated analysis. Not financial advice.

SOUTH SAN FRANCISCO, Calif., March 27, 2026 (GLOBE NEWSWIRE) -- Senti Biosciences, Inc. (Nasdaq: SNTI) (“Senti Bio”), a clinical-stage biotechnology company developing next-generation cell and gene therapies using its proprietary Gene Circuit platform, today reported financial results for the fourth quarter of 2025 and full year 2025 and provided a summary of recent pipeline and corporate highlights.

“2025 was a year of important progress for Senti as we continued to advance our mission of developing next-generation cell and gene therapies powered by our synthetic biology platform. Over the past year, we have strengthened the clinical and translational foundation of our pipeline, with SENTI-202 as the lead program generating positive clinical data, while continuing to refine and expand the capabilities of our Gene Circuit platform. We remain focused on disciplined execution, advancing our key programs toward critical development milestones and positioning Senti to deliver smarter, more selective medicines for patients with serious diseases. I am proud of our team’s commitment and believe the progress we made in 2025 positions us well for the opportunities ahead,” commented Timothy Lu, MD, PhD, Co-Founder and CEO of Senti Biosciences.

RECENT PIPELINE AND CORPORATE UPDATES

  • Reported updated positive preliminary clinical data from the ongoing Phase 1 trial of SENTI-202 in relapsed/refractory acute myeloid leukemia (AML), demonstrating encouraging response rates, durability, and a favorable safety profile;
  • Received Regenerative Medicine Advanced Therapy (RMAT) designation from the U.S. Food and Drug Administration for SENTI-202 for the treatment of adults with relapsed or refractory AML;
  • Continued advancement of the Company’s pipeline and synthetic biology platform, including progress across its Gene Circuit–engineered cell therapy programs; and
  • Maintained focus on disciplined capital management to support pipeline execution and key development milestones.

YEAR 2025 FINANCIAL RESULTS

  • Cash and Cash Equivalents: As of December 31, 2025, Senti Bio held cash and cash equivalents of approximately $16.4 million.
  • R&D Expenses: Research and development expenses were $7.8 million for both of the three months ended December 31, 2025 and 2024, respectively. For the full year of 2025, research and development expenses were $37.6 million.
  • G&A Expenses: General and administrative expenses were $5.8 million and $8.4 million for the quarter ended December 31, 2025 and 2024, respectively. The decrease of $2.6 million was primarily due to a decrease of $2.3 million in external services and supplies cost and a decrease of $0.7 million in facilities and other costs, partially offset by an increase of $0.4 million in personnel-related expenses. For the full year of 2025, general and administrative expenses were $26.2 million.
  • Net Loss: Net loss was $14.5 million, or $0.53 per basic and diluted share, for the three months ended December 31, 2025. Net loss for the full-year 2025 was $61.4 million, or $2.73 per share. Net loss for the year ended December 31, 2025 included a non-recurring $5.1 million impairment of long-lived assets as well as non-cash stock-based compensation expense of $5.7 million.

About Senti Bio 

Senti Bio is a clinical stage biotechnology company developing a new generation of cell and gene therapies for patients living with incurable diseases. To achieve this, Senti Bio is leveraging its synthetic biology platform to engineer Gene Circuits into new medicines with enhanced precision and control. These Gene Circuits are designed to precisely kill cancer cells, to spare healthy cells, to increase specificity to target tissues, and/or to be controllable even after administration. The Company’s wholly-owned pipeline comprises cell therapies engineered with Gene Circuits to target challenging liquid and solid tumor indications. Senti’s Gene Circuits have been shown preclinically to work in both NK and T cells. Senti Bio has also preclinically demonstrated the potential breadth of Gene Circuits in other modalities and diseases outside of oncology and continues to advance these capabilities through partnerships. 

Forward-Looking Statements
This press release and document contain certain statements that are not historical facts and are considered forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. These forward-looking statements generally are identified by the words “believe,” “could,” “predict,” “continue,” “ongoing,” “project,” “expect,” “anticipate,” “estimate,” “intend,” “strategy,” “future,” “opportunity,” “plan,” “may,” “should,” “will,” “would,” “will be,” “will continue,” “will likely result,” “forecast,” “seek,” “target” and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. Forward-looking statements are predictions, projections, and other statements about future events that are based on current expectations of Senti Bio’s management and assumptions, whether or not identified in this document, and, as a result, are subject to risks and uncertainties. Forward-looking statements include, but are not limited to, expectations regarding Senti Bio’s future results. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as and must not be relied on by any investor as, a guarantee, an assurance, a prediction, or a definitive statement of fact or probability. Actual events and circumstances are difficult or impossible to predict and will differ from assumptions. Many actual events and circumstances are beyond the control of Senti Bio. Many factors could cause actual future results to differ materially from the forward-looking statements in this document, including but not limited to: (i) changes in domestic and foreign business, market, financial, political and legal conditions, (ii) changes in the competitive and highly regulated industries in which Senti Bio operates, variations in operating performance across competitors, changes in laws and regulations affecting Senti Bio’s business, (iii) the ability to implement business plans, forecasts and other expectations, (iv) the risk of downturns and a changing regulatory landscape in Senti Bio’s highly competitive industry, (v) risks relating to the uncertainty of any projected financial information with respect to Senti Bio, (vi) risks related to uncertainty in the timing or results of Senti Bio’s , clinical studies, patient enrollment, and GMP manufacturing startup activities, (vii) Senti Bio’s dependence on third parties in connection with clinical studies, and GMP manufacturing activities, (viii) risks related to delays and other impacts from macroeconomic and geopolitical events, increasing rates of inflation and rising interest rates on business operations, (ix) risks related to the timing and utilization of the grant from CIRM, and (x) the success of any future research and development efforts by Senti Bio. The foregoing list of factors is not exhaustive. You should carefully consider the foregoing factors and the other risks and uncertainties described in the “Risk Factors” section of Senti Bio’s most recent periodic report filed with the U.S. Securities and Exchange Commission (“SEC”), and other documents filed by Senti Bio from time to time with the SEC. These filings identify and address other important risks and uncertainties that could cause actual events and results to differ materially from those contained in the forward-looking statements in this document. There may be additional risks that Senti Bio does not presently know, or that Senti Bio currently believes are immaterial that could also cause actual results to differ from those contained in the forward-looking statements in this document. Forward-looking statements speak only as of the date they are made. Senti Bio anticipates that subsequent events and developments may cause Senti Bio’s assessments to change. Except as required by law, Senti Bio assumes no obligation to update publicly any forward-looking statements, whether as a result of new information, future events, or otherwise.

Availability of Other Information About Senti Biosciences, Inc. 
 
For more information, please visit the Senti Bio website at www.sentibio.com or follow Senti Bio on X (@SentiBio) and LinkedIn (Senti Biosciences). Investors and others should note that we communicate with our investors and the public using our company website (www.sentibio.com), including, but not limited to, company disclosures, investor presentations and FAQs, Securities and Exchange Commission filings, press releases, public conference call transcripts and webcast transcripts, as well as on X and LinkedIn. The information that we post on our website or on X or LinkedIn could be deemed to be material information. As a result, we encourage investors, the media and others interested to review the information that we post there on a regular basis. The contents of our website or social media shall not be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended.

Investor Contact:
JTC Team, LLC
Jenene Thomas
(908) 824-0775
SNTI@jtcir.com

Senti Biosciences, Inc.
Unaudited Selected Consolidated Balance Sheet Data
(in thousands)
    
 December 31, December 31,
 2025
 2024
Cash and cash equivalents$16,420  $48,277 
Total assets 51,223   97,841 
Total liabilities 45,634   47,086 
Series A redeemable convertible preferred stock    25,106 
Accumulated deficit (358,572)  (297,134)
Total stockholders’ equity 5,589   25,649 
        


Senti Biosciences, Inc.
Unaudited Condensed Consolidated Statements of Operations and Comprehensive Loss
(In thousands, except share and per share amounts)
    
 Three Months Ended
December 31,
 Year Ended
December 31,
 2025 2024 2025 2024
Revenue$22  $  $22  $ 
Operating expenses:       
Research and development (including related party costs of $1,836 and $3,207 for the three months ended December 31, 2025 and 2024, respectively, and $12,909 and $14,266 for the year ended December 31, 2025 and 2024, respectively) 7,760   7,772   37,586   34,356 
General and administrative 5,846   8,395   26,163   26,370 
Impairment of long-lived assets 5,052      5,052   313 
Total operating expenses 18,658   16,167   68,801   61,039 
Loss from operations (18,636)  (16,167)  (68,779)  (61,039)
Other income (expense):       
Interest income 97   230   927   948 
GeneFab sublease income - related party 3,691   1,744   5,423   6,449 
Other income, net - related party 160      160    
Other income, net 221   159   831   153 
Change in fair value of Preferred Stock Tranche Liability - related party    13,404      13,404 
Change in fair value of GeneFab Option - related party          6,331 
Change in fair value of contingent earnout liability    20      20 
Change in fair value of GeneFab Economic Share - related party          (1,816)
Change in fair value of GeneFab Note Receivable - related party          (17,240)
Total other income, net$4,169  $15,557  $7,341  $8,249 
Net loss$(14,467) $(610) $(61,438) $(52,790)
Comprehensive loss$(14,467) $(610) $(61,438) $(52,790)
Basic and diluted net loss per share$(0.53) $(0.67) $(2.73) $(12.03)
Basic and diluted weighted-average number of shares used in computing net loss per share 27,380,373   4,661,085   22,483,391   4,595,946 
                

FAQ

What does the FDA RMAT designation for SENTI-202 mean for SNTI investors?

It signals expedited development and regulatory support for SENTI-202, potentially accelerating review timelines. According to the company, RMAT was granted for SENTI-202 in relapsed/refractory AML, which may streamline interactions with FDA during late‑stage development.

How much cash did Senti Biosciences (SNTI) report at December 31, 2025?

Senti reported approximately $16.4 million in cash and cash equivalents at year‑end 2025. According to the company, this balance supports near‑term operations but will be a consideration for funding future development milestones.

What were SNTI's reported net losses for Q4 2025 and full‑year 2025?

Net loss was $14.5M in Q4 2025 and $61.4M for full‑year 2025. According to the company, FY2025 results included a $5.1M non‑recurring impairment and $5.7M of non‑cash stock‑based compensation.

What clinical progress did Senti (SNTI) report for SENTI-202 in March 2026?

The company reported updated positive preliminary Phase 1 data showing encouraging response rates, durability, and a favorable safety profile. According to the company, these results support SENTI-202 as the lead program in AML development.

How did SNTI's operating expenses change in Q4 2025 compared with Q4 2024?

R&D expense remained unchanged at $7.8M quarter‑over‑quarter; G&A decreased by $2.6M. According to the company, the G&A decline reflected lower external services and facilities costs, partially offset by higher personnel expenses.
Senti Bioscience

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23.16M
11.47M
Biotechnology
Biological Products, (no Diagnostic Substances)
Link
United States
SOUTH SAN FRANCISCO