STOCK TITAN

Century Therapeutics Reports Full Year 2025 Financial Results and Business Updates

Rhea-AI Impact
(High)
Rhea-AI Sentiment
(Positive)
Tags

Century Therapeutics (NASDAQ: IPSC) reported full-year 2025 results and pipeline progress on March 12, 2026. Key news: CNTY-813 is in IND-enabling studies with an IND submission expected in 4Q 2026 and initial clinical data anticipated in 2H 2027. CNTY-308 is advancing toward clinical entry in 2026. The company completed an oversubscribed $135 million private placement and says cash runway is extended into 1Q 2029. 2025 financials: cash and investments of $117.1 million, collaboration revenue of $109.2 million, R&D $95.7 million, G&A $24.0 million, and net loss of $9.6 million.

Loading...
Loading translation...

Positive

  • Cash runway extended into 1Q 2029 after an oversubscribed $135M private placement
  • Collaboration revenue $109.2M in 2025 from Bristol-Myers Squibb collaboration
  • CNTY-813 on track for IND submission in 4Q 2026 with initial data expected 2H 2027
  • GMP Master Cell Bank for CNTY-813 manufacturing completed
  • CNTY-308 advancing toward projected clinical entry in 2026
  • Net loss narrowed to $9.6M in 2025 from $126.6M in 2024

Negative

  • Cash, cash equivalents, and marketable securities declined to $117.1M at 12/31/2025 from $220.1M a year earlier
  • Net cash used in operations remained high at $103.9M for 2025
  • Revenue concentration risk: $109.2M of 2025 revenue tied to a single collaboration with Bristol-Myers Squibb

News Market Reaction – IPSC

-8.42%
21 alerts
-8.42% News Effect
-18.3% Trough in 6 hr 14 min
-$45M Valuation Impact
$490M Market Cap
1.4x Rel. Volume

On the day this news was published, IPSC declined 8.42%, reflecting a notable negative market reaction. Argus tracked a trough of -18.3% from its starting point during tracking. Our momentum scanner triggered 21 alerts that day, indicating elevated trading interest and price volatility. This price movement removed approximately $45M from the company's valuation, bringing the market cap to $490M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Cash & securities: $117.1 million Prior-year cash: $220.1 million Net cash used ops 2025: $103.9 million +5 more
8 metrics
Cash & securities $117.1 million Cash, cash equivalents and marketable securities as of Dec 31, 2025
Prior-year cash $220.1 million Cash, cash equivalents and marketable securities as of Dec 31, 2024
Net cash used ops 2025 $103.9 million Net cash used in operations for year ended Dec 31, 2025
Collaboration revenue 2025 $109.2 million Bristol-Myers Squibb collaboration revenue for year ended Dec 31, 2025
R&D expenses 2025 $95.7 million Research and development expenses for year ended Dec 31, 2025
G&A expenses 2025 $24.0 million General and administrative expenses for year ended Dec 31, 2025
Net loss 2025 $9.6 million Net loss for year ended Dec 31, 2025
Private placement $135 million Oversubscribed private placement completed January 2026 extending runway into 1Q 2029

Market Reality Check

Price: $2.34 Vol: Volume 1,043,290 is in li...
normal vol
$2.34 Last Close
Volume Volume 1,043,290 is in line with 20-day average of 1,034,213 (relative volume 1.01x). normal
Technical Shares at $2.73 are above the 200-day MA of $0.92, trading 10.2% below the 52-week high of $3.04 and well above the 52-week low of $0.3418.

Peers on Argus

Biotech peers show mixed moves: BCAB -6.87%, BRNS -6.48%, TPST -0.83% while PSTV...
1 Up 1 Down

Biotech peers show mixed moves: BCAB -6.87%, BRNS -6.48%, TPST -0.83% while PSTV +1.15% and RENB +19.33%. Momentum scanner flags SNTI +0.99% and ACRV -1.84% in opposite directions. With target direction unset and peers split, current setup points to stock‑specific factors rather than a broad sector rotation.

Previous Earnings Reports

5 past events · Latest: Nov 13 (Negative)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Nov 13 Q3 2025 earnings Negative -17.5% Quarterly loss and trial discontinuation alongside pipeline updates and runway guidance.
Aug 14 Q2 2025 earnings Positive +2.1% Pipeline progress, extended cash runway after workforce reduction, and stable cash reserves.
May 15 Q1 2025 earnings Positive +8.2% Net income driven by collaboration revenue and a solid cash position supporting R&D.
Mar 19 FY 2024 results Negative -5.7% Full‑year net loss with increased R&D despite a strong cash balance and pipeline shift.
Nov 05 Q3 2024 earnings Positive +5.6% Encouraging CNTY‑101 response data and ample cash extending runway into H2 2026.
Pattern Detected

Across the last five earnings or financial result releases, share price moves have consistently aligned with the tone of the announcements, with negative updates seeing declines and more constructive quarters trading higher.

Recent Company History

Over the past several earnings cycles, Century has steadily repositioned its pipeline while managing its balance sheet. Earlier updates in 2025 highlighted strong collaboration revenue, periods of net income, and extended cash runway, supporting development of CNTY‑101 and CNTY‑308. However, full year 2024 and Q3 2025 still carried sizeable net losses and trial discontinuations, which coincided with negative price reactions. Today’s full year 2025 results continue this narrative of pipeline focus and improving loss profile alongside a reinforced cash position.

Historical Comparison

-1.4% avg move · Across the last five earnings‑tagged releases, IPSC moved an average of -1.45%. This full year 2025 ...
earnings
-1.4%
Average Historical Move earnings

Across the last five earnings‑tagged releases, IPSC moved an average of -1.45%. This full year 2025 update fits the pattern of financial results tied closely to pipeline milestones and cash runway visibility.

Earnings updates have tracked a shift from CNTY‑101 oncology focus toward autoimmune programs CNTY‑813 and CNTY‑308, while cash runway has progressed from H2 2026 into Q4 2027 and now, with new financing, into 1Q 2029.

Regulatory & Risk Context

Active S-3 Shelf
Shelf Active
Active S-3 Shelf Registration 2026-02-05

An effective S-3 shelf registration dated Feb 5, 2026 covers 176,086,947 shares of common stock for resale by existing investors from a January 2026 private placement. The company does not receive proceeds from these stockholder sales but may receive cash if associated warrants are exercised. As of the latest data, there is no recorded usage of this shelf.

Market Pulse Summary

The stock moved -8.4% in the session following this news. A negative reaction despite the reported i...
Analysis

The stock moved -8.4% in the session following this news. A negative reaction despite the reported improvements would fit prior patterns where earnings tied to losses and trial changes weighed on sentiment. While full year 2025 shows a sharply reduced net loss of $9.6M and lower operating expenses, cash declined to $117.1M before the $135M financing. The active S-3 registration for 176,086,947 resale shares may also color perceptions of potential overhang even though the company does not receive proceeds from stockholder sales.

Key Terms

investigational new drug (ind), ind-enabling studies, car-it cell therapy, phase 1/2, +3 more
7 terms
investigational new drug (ind) regulatory
"CNTY-813... in Investigational New Drug (IND)-enabling studies; IND submission expected"
An investigational new drug (IND) is a drug or biologic that is being tested but has not yet been approved for general use; it is the application and formal status that allows a company to begin human clinical trials under regulator oversight. Investors care because an IND marks the transition from lab work to human testing — like getting a permit to run real-world experiments — which creates important milestones, costs, timelines and regulatory risk that drive a development-stage company's value.
ind-enabling studies regulatory
"CNTY-813... in Investigational New Drug (IND)-enabling studies; IND submission expected"
Ind-enabling studies are early research efforts that test whether a new drug or treatment is safe and effective enough to move forward in development. They are like preliminary tests to ensure a product works as intended before investing more resources into large-scale trials. For investors, these studies are important because successful results can signal potential progress toward bringing a new product to market, impacting its future value.
car-it cell therapy medical
"CNTY-308, a CD19-targeted CAR-iT cell therapy engineered with Allo-Evasion™ 5.0"
CAR‑T cell therapy is a cancer treatment that takes a patient’s immune cells, reprograms them to recognize a specific marker on tumor cells, and returns them to the body so they can hunt down and kill cancer like trained guard dogs guided by a new scent. It matters to investors because these therapies can command high prices and large market demand if approved, but they also carry costly development, complex manufacturing and safety risks that can drive big swings in a company’s value.
phase 1/2 medical
"ongoing CARAMEL study, a Phase 1/2 investigator-sponsored trial (IST) led by"
Phase 1/2 is a combined early-stage clinical trial that first tests a new drug or treatment for safety and the right dose, then quickly expands to check if it shows any signs of working in patients. For investors, results from a Phase 1/2 study offer an early read on both risk and potential reward—like a prototype test that both confirms a product won’t harm users and suggests whether it could sell—helping guide valuation and development decisions.
investigator-sponsored trial (ist) medical
"CARAMEL study, a Phase 1/2 investigator-sponsored trial (IST) led by Professors"
An investigator-sponsored trial (IST) is a clinical study initiated and led by an independent researcher or physician rather than by a company that makes the drug or device being tested. It matters to investors because ISTs can produce independent data that may confirm or challenge a product’s safety or benefit, act as a lower-cost way to explore new uses, and affect regulatory and commercial prospects much like an independent customer trial influencing market confidence.
gmp master cell bank technical
"completion of the manufacturing of a GMP Master Cell Bank for CNTY-813, along with"
A GMP master cell bank is a carefully characterized, frozen stock of cells created and stored under Good Manufacturing Practice standards to serve as the single, controlled source for making a biological drug or vaccine. Think of it as the official seed supply for manufacturing: it ensures each production run starts from the same, tested material, which matters to investors because it underpins product consistency, regulatory approval, supply reliability and reduced production risk.
private placement financial
"oversubscribed $135 million private placement in January 2026"
A private placement is a way for companies to raise money by selling securities directly to a small group of investors instead of through a public offering. This process is often quicker and less regulated, making it similar to offering a special, exclusive investment opportunity to select individuals or institutions. For investors, it can provide access to unique investment options that are not available on public markets.

AI-generated analysis. Not financial advice.

  • CNTY-813, lead beta islet cell therapy program as a potential functional cure for type 1 diabetes, in Investigational New Drug (IND)-enabling studies; IND submission expected in 4Q 2026 to support anticipated initial clinical data in 2H 2027
  • CNTY-308, a CD19-targeted CAR-iT cell therapy engineered with Allo-Evasion™ 5.0, on track to enter the clinic in 2026
  • Strengthened balance sheet and cash runway extended into 1Q 2029 from oversubscribed $135 million private placement in January 2026

PHILADELPHIA, March 12, 2026 (GLOBE NEWSWIRE) -- Century Therapeutics, Inc. (‘Century’, NASDAQ: IPSC), a biotechnology company developing induced pluripotent stem cell (iPSC)-derived cell therapies for autoimmune diseases, including type 1 diabetes, and cancer, today reported financial results for the full year ended December 31, 2025, and recent business highlights.

“Century entered 2026 with strong momentum, fueled by the successful completion of our $135 million private placement and continued focus on advancing our prioritized programs closer to patients living with significant unmet medical need,” said Brent Pfeiffenberger, Pharm.D., Chief Executive Officer of Century Therapeutics. “We are moving fast and executing with precision on CNTY-813, our top priority and a program we believe has the potential to functionally cure type 1 diabetes. Recent achievements, including compelling preclinical results combined with constructive interactions with the FDA, strengthen our confidence in the clinical path ahead. We plan to submit an IND as early as the fourth quarter of this year and anticipate initial clinical data in the second half of 2027. We are energized by the progress across our pipeline, confident in the road ahead, and focused on advancing our most promising programs into the clinic.”

Fourth Quarter 2025 and Recent Highlights

Pipeline

  • CNTY-813, priority program for type 1 diabetes, advancing through IND-enabling activities and tracking toward planned IND submission in 2026: Century continues to advance IND-enabling studies for its lead pipeline program, CNTY-813, a beta islet replacement therapy with Allo-Evasion™ 5.0 as a potential functional cure for type 1 diabetes. To date, Century has generated compelling preclinical data for CNTY-813, demonstrating high potency and long duration for functional glucose control and protection against immune rejection via Allo-Evasion™ 5.0 engineering to potentially minimize or eliminate the need for chronic immunosuppression. This data package, which includes the maintenance of normoglycemia in animal models for more than 6 months, completion of the manufacturing of a GMP Master Cell Bank for CNTY-813, along with recent engagement with the U.S. Food and Drug Administration (FDA), has reinforced the company’s belief in an efficient pathway to IND submission for CNTY-813. Century expects to submit an IND for the program in the fourth quarter of 2026 and anticipates initial clinical data in the second half of 2027.
  • CNTY-308 advancing in IND-enabling studies for projected clinical entry in 2026: Century continues to make progress in IND-enabling studies with CNTY-308, a CD19-targeted CD4+/CD8+ ab CAR-iT cell therapy with Allo-Evasion™ 5.0 as a potential treatment for B-cell-mediated diseases. In previously presented preclinical studies, CNTY-308 demonstrated functional comparability to primary CAR-T cells, including target-mediated proliferation, cytokine secretion, and long-term persistence. These data, coupled with the growing academic and industry experience with CAR-T treatment supporting its potential to deliver deep and durable responses in patients, reinforce Century’s belief in CNTY-308 to deliver autologous, CAR-T-like clinical benefits in an allogeneic, patient-centric format for enhanced treatment accessibility. Subject to completion of IND-enabling studies and regulatory clearance, Century expects CNTY-308 to enter the clinic in 2026.
  • Additional insights from ongoing CARAMEL IST expected in 2026: The company anticipates updated preliminary clinical data this year from the ongoing CARAMEL study, a Phase 1/2 investigator-sponsored trial (IST) led by Professors Georg Schett and Andreas Mackensen and sponsored by the Friedrich-Alexander University Erlangen-Nürnberg. Previously disclosed clinical data from the trial have demonstrated that CNTY-101 was generally well tolerated and exhibits a predictable biologic profile with early signs of clinical response in autoimmune diseases.

Corporate

  • Completed oversubscribed $135 million private placement financing: In January 2026, Century entered into a securities purchase agreement led by new investor TCGX with participation from additional new and existing investors, including RA Capital Management, Commodore Capital, Deep Track Capital, RTW Investments, Venrock Healthcare Capital Partners, and the T1D Fund. The gross proceeds were approximately $135 million before placement agent fees and offering expenses.
  • Appointed two new members to the Board of Directors: In December 2025, Han Lee, Ph.D., M.B.A., and Martin Murphy, Ph.D., were appointed to Century’s Board of Directors. As part of their appointments, Dr. Lee serves as a member of the Audit and the Compensation Committees and Dr. Murphy serves as Chair of the Compensation and a member of the Nominating and Corporate Governance Committees.

Full Year 2025 Financial Results

  • Cash Position: Cash, cash equivalents, and marketable securities were $117.1 million as of December 31, 2025, as compared to $220.1 million as of December 31, 2024. Net cash used in operations was $103.9 million for the year ended December 31, 2025, compared to net cash used in operations of $110.1 million for the year ended December 31, 2024. The company estimates its cash, cash equivalents, and investments as of December 31, 2025, together with the net proceeds raised after year end, will support operations into the first quarter of 2029.
  • Collaboration Revenue: Collaboration revenue generated through the company’s collaboration, option, and license agreement with Bristol-Myers Squibb was $109.2 million for the year ended December 31, 2025, compared to $6.6 million for the same period in 2024.
  • Research and Development (R&D) Expenses: R&D expenses were $95.7 million for the year ended December 31, 2025, compared to $107.2 million for the same period in 2024. The decrease in R&D expenses was primarily due to a reduction of personnel and manufacturing costs, offset by an increase in research and laboratory costs to progress clinical trials and preclinical programs.
  • General and Administrative (G&A) Expenses: G&A expenses were $24.0 million for the year ended December 31, 2025, compared to $33.2 million for the same period in 2024. The decrease was primarily the result of a decrease in legal fees associated with the Clade acquisition in 2024, a gain on lease modification, a gain on reduction of contingent consideration liability, and a decrease in stock-based compensation.
  • Net Loss: Net loss was $9.6 million for the year ended December 31, 2025, compared to net loss of $126.6 million for the same period in 2024.

About Century Therapeutics
Century Therapeutics (NASDAQ: IPSC) is a biotechnology company advancing a pipeline of induced pluripotent stem cell (iPSC)-derived cell therapies with the potential to meaningfully address autoimmune diseases, including type 1 diabetes, and cancer. The company’s therapies are derived from its iPSC cell foundry and leverage its novel immune evasion engineering technology, Allo-Evasion™. Century believes its approach to developing off-the-shelf cell therapies will expand patient access and provide advantages over existing cell therapies which will ultimately advance the course of care. For more information on Century Therapeutics, please visit www.centurytx.com and connect with us on LinkedIn.

Forward-Looking Statements
This press release contains forward-looking statements within the meaning of, and made pursuant to the safe harbor provisions of, The Private Securities Litigation Reform Act of 1995. All statements contained in this press release, other than statements of historical facts or statements that relate to present facts or current conditions, including but not limited to, statements our timing and expectations regarding our preclinical and clinical development programs, including their planned development, therapeutic potential and market opportunity, ongoing and planned regulatory interactions, the achievement of developmental milestones, corporate strategies, and our financial resources and expected cash runway are forward-looking statements. These statements involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance, or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements. In some cases, you can identify forward-looking statements by terms such as “may,” “might,” “will,” “should,” “expect,” “plan,” “aim,” “seek,” “anticipate,” “could,” “intend,” “target,” “project,” “contemplate,” “believe,” “estimate,” “predict,” “forecast,” “potential” or “continue” or the negative of these terms or other similar expressions. The forward-looking statements in this press release are only predictions. We have based these forward-looking statements largely on our current expectations and projections about future events and financial trends that we believe may affect our business, financial condition, and results of operations. These forward-looking statements speak only as of the date of this press release and are subject to a number of risks, uncertainties and assumptions, some of which cannot be predicted or quantified and some of which are beyond our control, including, among others: our ability to successfully advance our current and future product candidates through development activities, preclinical studies, and clinical trials; our ability to meet development milestones on anticipated timelines; uncertainties inherent in the results of preliminary data, pre-clinical studies and earlier-stage clinical trials, which may not be predictive of final results or the results of later-stage clinical trials; our ability to obtain clearance of our future IND or CTA submissions and commence and complete clinical trials on expected timelines, or at all; our reliance on the maintenance of certain key collaborative relationships for the manufacturing and development of our product candidates; the timing, scope and likelihood of regulatory filings and approvals, including final regulatory approval of our product candidates; the impact of geopolitical issues, trade disputes and tariffs, banking instability and inflation on our business and operations, supply chain and labor force; the performance of third parties in connection with the development of our product candidates, including third parties conducting our clinical trials as well as third-party suppliers and manufacturers; our ability to successfully commercialize our product candidates and develop sales and marketing capabilities, if our product candidates are approved; our ability to recruit and maintain key members of management and our ability to maintain and successfully enforce adequate intellectual property protection. These and other risks and uncertainties are described more fully in the “Risk Factors” section of our most recent filings with the Securities and Exchange Commission and available at www.sec.gov. You should not rely on these forward-looking statements as predictions of future events. The events and circumstances reflected in our forward-looking statements may not be achieved or occur, and actual results could differ materially from those projected in the forward-looking statements. Moreover, we operate in a dynamic industry and economy. New risk factors and uncertainties may emerge from time to time, and it is not possible for management to predict all risk factors and uncertainties that we may face. Except as required by applicable law, we do not plan to publicly update or revise any forward-looking statements contained herein, whether as a result of any new information, future events, changed circumstances or otherwise.

For More Information:

Century Therapeutics
Douglas Carr
Senior Vice President, Finance
investor.relations@centurytx.com

JPA Health
Sarah McCabe
smccabe@jpa.com

 
Century Therapeutics, Inc
Condensed Balance Sheets
(unaudited, in thousands)
        
 December 31, December 31,
Assets2025 2024
Current Assets:$  $ 
Cash and cash equivalents 61,853   58,441 
Short-term investments 55,261   130,851 
Prepaid expenses and other current assets 3,655   4,759 
Total current assets 120,769   194,051 
Property and equipment, net 50,026   62,141 
Operating lease right-of-use assets, net 16,139   28,706 
Long-term investments -   30,818 
Intangible assets 34,200   34,200 
Other long-term assets 2,570   3,300 
Total assets$223,704  $353,216 
      
Liabilities, convertible preferred stock, and stockholders' equity   
Current liabilities:     
Accounts payable$4,773  $3,075 
Accrued expenses and other liabilities 11,696   17,543 
Contingent consideration liability, short term 3,757   - 
Deferred revenue, current -   109,164 
Total current liabilities 20,226   129,782 
Operating lease liability, noncurrent 40,241   48,960 
Contingent consideration liability, long term -   8,738 
Deferred tax liability 4,301   4,374 
Total liabilities 64,768   191,854 
Stockholders' equity     
Preferred stock -   - 
Common stock 9   9 
Additional paid-in capital 950,814   943,366 
Accumulated deficit (791,917)  (782,337)
Accumulated other comprehensive loss 30   324 
Total stockholders' equity 158,936   161,362 
Total liabilities and stockholders' equity$223,704  $353,216 
        


Century Therapeutics, Inc
Condensed consolidated statements of operations
(unaudited, in thousands, except share and per share amounts)
        
 Year Ended Year Ended
 December 31,
2025
 December 31,
2024
Collaboration Revenue$109,164  $6,589 
      
Operating Expenses     
Research and development 95,667   107,244 
General and administrative 24,003   33,155 
Impairment of long-lived assets 6,763   - 
Impairment of goodwill -   4,327 
Total operating expenses 126,433   144,726 
      
Income (loss) from operations (17,269)  (138,137)
      
Interest income 7,346   13,007 
Other income, net 275   354 
Loss before (benefit) provision for income taxes (9,648)  (124,776)
(Benefit) provision for income taxes (68)  1,790 
Net Loss$(9,580) $(126,566)
      
Unrealized gain (loss) on investments (294)  153 
Foreign currency translation adjustment gain (loss) -   63 
Comprehensive loss$(9,874) $(126,350)
      
Net loss per common share
Basic and Diluted
 (0.14)  (1.61)
      
Weighted average common shares outstanding
Basic and Diluted
 86,556,515   78,648,958 
        

FAQ

When does Century Therapeutics (IPSC) expect to submit an IND for CNTY-813?

Century expects to submit an IND for CNTY-813 in the fourth quarter of 2026. According to the company, IND-enabling studies are underway and the program completed GMP Master Cell Bank manufacturing to support a 4Q 2026 filing.

What clinical data timeline does Century (IPSC) project for CNTY-813?

Initial clinical data for CNTY-813 is anticipated in the second half of 2027. According to the company, preclinical data showed normoglycemia beyond six months and recent FDA engagement supports the planned timeline.

How did Century Therapeutics (IPSC) extend its cash runway into 1Q 2029?

Century extended its cash runway into the first quarter of 2029 after an oversubscribed $135 million private placement. According to the company, net proceeds plus year-end cash and investments support operations into 1Q 2029.

What drove Century's $109.2 million collaboration revenue in 2025 (IPSC)?

The $109.2 million in 2025 collaboration revenue was generated under the Bristol-Myers Squibb collaboration agreement. According to the company, that agreement produced substantially higher collaboration revenue versus 2024's $6.6 million.

When is CNTY-308 expected to enter the clinic for IPSC investors?

Century projects CNTY-308 to enter the clinic in 2026, subject to IND-enabling study completion and regulatory clearance. According to the company, preclinical comparability data support progression to a clinical timeline in 2026.

What were Century Therapeutics' (IPSC) key 2025 financial metrics investors should note?

Key 2025 metrics: cash and investments $117.1M, collaboration revenue $109.2M, R&D $95.7M, G&A $24.0M, and net loss $9.6M. According to the company, these figures reflect financing, collaboration receipts, and program spending in 2025.
Century Therapeutics, Inc.

NASDAQ:IPSC

View IPSC Stock Overview

IPSC Rankings

IPSC Latest News

IPSC Latest SEC Filings

IPSC Stock Data

218.51M
156.29M
Biotechnology
Biological Products, (no Diagnostic Substances)
Link
United States
PHILADELPHIA