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Keros Therapeutics Reports Recent Business Highlights and Fourth Quarter and Full Year 2025 Financial Results

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Keros (Nasdaq: KROS) reported fourth-quarter 2025 net loss of $23.5M and full-year 2025 net income of $87.0M, driven largely by revenue from a license agreement with Takeda. The company expects to start a Phase 2 trial of rinvatercept in DMD in Q2 2026 and to engage regulators on an ALS Phase 2 design in H2 2026. Cash and cash equivalents were $287.4M at year-end, with management saying this funding is expected to support operations into the first half of 2028.

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Positive

  • Net income of $87.0M for full-year 2025
  • Phase 2 DMD trial expected to commence in Q2 2026
  • Cash runway projected into the first half of 2028
  • R&D expense decreased to $129.6M for 2025 from $173.6M

Negative

  • Cash balance declined to $287.4M from $559.9M at year-end 2024
  • General and administrative expenses rose to $46.8M in 2025
  • Revenue concentration reliance on Takeda license drove 2025 profitability

Market Reaction – KROS

-13.51% $11.91
15m delay 15 alerts
-13.51% Since News
$11.91 Last Price
$11.91 $13.09 Day Range
-$57M Valuation Impact
$363M Market Cap
0.4x Rel. Volume

Following this news, KROS has declined 13.51%, reflecting a significant negative market reaction. Our momentum scanner has triggered 15 alerts so far, indicating notable trading interest and price volatility. The stock is currently trading at $11.91. This price movement has removed approximately $57M from the company's valuation.

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

Key Figures

Q4 2025 net loss: $23.5M FY 2025 net income: $87.0M FY 2024 net loss: $187.4M +5 more
8 metrics
Q4 2025 net loss $23.5M Fourth quarter 2025 net loss vs prior-year Q4 loss
FY 2025 net income $87.0M Full year 2025 result vs FY 2024 net loss
FY 2024 net loss $187.4M Full year 2024 net loss baseline for comparison
FY 2025 R&D expenses $129.6M Research and development, year ended Dec 31, 2025
FY 2024 R&D expenses $173.6M Research and development, year ended Dec 31, 2024
FY 2025 G&A expenses $46.8M General and administrative, year ended Dec 31, 2025
Cash & equivalents 12/31/2025 $287.4M Cash and cash equivalents as of Dec 31, 2025
Runway guidance into 1H 2028 Expected funding of operating and capital needs based on 12/31/2025 cash

Market Reality Check

Price: $13.77 Vol: Volume 338,349 is modestl...
normal vol
$13.77 Last Close
Volume Volume 338,349 is modestly above 20-day average 311,507 (relative volume 1.09x). normal
Technical Shares at $13.40 trade below 200-day MA of $16.10, 40.58% below 52-week high and 46.93% above 52-week low.

Peers on Argus

KROS fell 3.67% while peers were mixed: ANAB -1.44%, BCAX -0.28%, RIGL -3.22%, P...

KROS fell 3.67% while peers were mixed: ANAB -1.44%, BCAX -0.28%, RIGL -3.22%, PVLA +1.04%, TYRA +5.13%. The move appears more stock-specific than sector-driven.

Previous Earnings Reports

5 past events · Latest: Nov 05 (Positive)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Nov 05 Q3 2025 earnings Positive +3.3% Smaller net loss, Takeda revenue, reduced R&D costs, strong cash and pipeline plans.
Aug 06 Q2 2025 earnings Positive -7.3% Improved net loss, solid cash, capital return plan and KER-065 Phase 2 plans.
May 06 Q1 2025 earnings Positive -0.4% Net income, stronger cash, KER-065 progress and upcoming TROPOS trial data.
Feb 26 FY 2024 earnings Neutral +0.6% Large net losses but higher revenue, Takeda upfront and extended cash runway.
Nov 06 Q3 2024 earnings Neutral +1.1% Higher net loss with increased R&D but strong cash and trial enrollment progress.
Pattern Detected

Earnings releases have produced modest average moves (-0.52%), with mostly positive fundamentals but mixed price reactions, including both rallies and selloffs.

Recent Company History

Over the past five earnings cycles (Nov 2024–Nov 2025), Keros moved from larger net losses toward improved results, including periods of net income and strengthened cash positions. Revenue from the Takeda license and shifting elritercept R&D costs to Takeda feature prominently across multiple quarters. Management also initiated a $375M capital return program while extending cash runway into at least 2028. Today’s Q4/FY 2025 update continues themes of Takeda-related revenue, lower R&D versus 2024, and reiterated runway into the first half of 2028.

Historical Comparison

-0.5% avg move · Across five prior earnings releases, average next-day move was -0.52% with mixed tape reactions. Tod...
earnings
-0.5%
Average Historical Move earnings

Across five prior earnings releases, average next-day move was -0.52% with mixed tape reactions. Today’s -3.67% slide is a larger-than-usual downside move versus that history.

Earnings updates since late 2024 show a progression from sizable net losses toward improved results, reinforced cash runway out to at least 2028, Takeda-driven revenue, and capital returns, alongside continued advancement of KER-065 and elritercept.

Market Pulse Summary

The stock is dropping -13.5% following this news. A negative reaction despite FY 2025 net income of ...
Analysis

The stock is dropping -13.5% following this news. A negative reaction despite FY 2025 net income of $87.0M and affirmed runway into the first half of 2028 fits a pattern of mixed tape responses to Keros’ earnings, where the average move has been just -0.52%. The market may have focused on the reduced year-end cash balance of $287.4M after capital returns, or on ongoing R&D and G&A spending levels, even as Takeda-related revenue and pipeline plans continue to underpin the long-term story.

Key Terms

duchenne muscular dystrophy, amyotrophic lateral sclerosis, transforming growth factor-beta, cash tender offer
4 terms
duchenne muscular dystrophy medical
"advancing rinvatercept into a Phase 2 clinical trial in patients with Duchenne muscular dystrophy"
A rare, inherited condition that progressively weakens muscles, Duchenne muscular dystrophy causes the body’s muscle fibers to break down over time, often leading to severe disability. For investors, it matters because the small, well-defined patient population, high unmet medical need and complex regulatory and pricing dynamics mean successes or failures in clinical trials, approvals, or therapies can have outsized effects on a company’s valuation and future revenue prospects.
amyotrophic lateral sclerosis medical
"design of a Phase 2 clinical trial in patients with amyotrophic lateral sclerosis"
A progressive disease in which nerve cells that control voluntary muscles gradually fail, leading to loss of movement, speech and eventually breathing — like an electrical wiring system in the body slowly shorting out. It matters to investors because there are few effective treatments, so clinical trial results, regulatory approvals, new therapies or diagnostics can rapidly change patient care, market opportunity and company valuations.
transforming growth factor-beta medical
"disorders that are linked to dysfunctional signaling of the transforming growth factor-beta"
Transforming growth factor-beta (TGF-β) is a naturally occurring signaling protein that helps control cell growth, inflammation and tissue repair, acting like a traffic cop that tells cells when to divide, change form or calm down. It matters to investors because drugs that block or boost TGF-β can treat cancers, fibrotic diseases and immune disorders, affecting clinical trial outcomes, regulatory risk and the commercial potential of biopharma assets.
cash tender offer financial
"cash and cash equivalents for the year was primarily driven by Keros’ share repurchase with certain stockholders and cash tender offer"
A cash tender offer is a public proposal in which an individual or group offers to buy a set number of a company's shares directly from shareholders for a specified cash price during a limited time. It matters to investors because it gives a clear, immediate chance to sell shares at a known price — like a store offering to buy back items at a posted rate — and can affect the stock’s market price, ownership control and liquidity.

AI-generated analysis. Not financial advice.

LEXINGTON, Mass., March 04, 2026 (GLOBE NEWSWIRE) -- Keros Therapeutics, Inc. (“Keros” or the “Company”) (Nasdaq: KROS), a clinical-stage biopharmaceutical company focused on developing and commercializing novel therapeutics to treat a wide range of patients with disorders that are linked to dysfunctional signaling of the transforming growth factor-beta (“TGF-ß”) family of proteins, today provided a business update and reported financial results for the fourth quarter and full year ended December 31, 2025.

“The previous year was an important period of transition for the Company, during which we sharpened our strategic priorities,” said Jasbir S. Seehra, Ph.D., President and Chief Executive Officer. “With that foundation in place, our attention is firmly on execution – advancing rinvatercept into a Phase 2 clinical trial in patients with Duchenne muscular dystrophy (“DMD”) and engaging regulators on the design of a Phase 2 clinical trial in patients with amyotrophic lateral sclerosis (“ALS”). With a strong foundation in place, our focus remains on bringing potential meaningful benefit to patients and creating long-term value for our stockholders.”

Recent Corporate Highlights:

  • Board and leadership changes:
    • In February 2026, Keros announced the appointment of Charles Newton to its board of directors, effective March 9, 2026. Concurrent with Mr. Newton joining Keros’ Board of Directors, Carl Gordon, Ph.D., C.F.A., will step down as a director of the Company.
    • Esther Cho, J.D., Senior Vice President, General Counsel, was promoted to Chief Legal Officer, effective February 24, 2026.

Selected Anticipated Program Milestones:

  • Rinvatercept for the treatment of DMD and for the treatment of ALS:
    • The Company expects to commence a Phase 2 clinical trial of rinvatercept in patients with DMD in the second quarter of 2026.
    • The Company plans to engage regulators on the design of a Phase 2 clinical trial of rinvatercept in patients with ALS in the second half of 2026.

2025 Financial Results

Keros reported a net loss of $23.5 million for the fourth quarter and net income of $87.0 million for the year ended December 31, 2025, as compared to a net loss of $46.0 million for the fourth quarter and a net loss of $187.4 million for the year ended December 31, 2024. The decrease in net loss for the fourth quarter and the net income for the year was largely due to revenue related to Keros’ license agreement with Takeda Pharmaceuticals U.S.A., Inc. (“Takeda”), partially offset by research and development efforts as well as additional investments to support the achievement of Keros’ clinical and corporate goals.

Research and development expenses were $17.9 million for the fourth quarter and $129.6 million for the year ended December 31, 2025, as compared to $45.6 million for the fourth quarter and $173.6 million for the year ended December 31, 2024. The decrease in research and development expenses for the fourth quarter and the year was primarily due to the transition of elritercept-related research and development expenses to Takeda.

General and administrative expenses were $11.7 million for the fourth quarter and $46.8 million for the year ended December 31, 2025, as compared to $10.7 million for the fourth quarter and $40.8 million for the year ended December 31, 2024. The increase in general and administrative expenses for the year was primarily due to an increase in external expenses, partially offset by a decrease in compensation costs, including stock-based compensation costs, in connection with a reduction in headcount.

Keros’ cash and cash equivalents as of December 31, 2025 was $287.4 million compared to $559.9 million as of December 31, 2024. The decrease in cash and cash equivalents for the year was primarily driven by Keros’ share repurchase with certain stockholders and cash tender offer. Based on current operating assumptions, Keros expects that its cash and cash equivalents as of December 31, 2025 will enable the Company to fund its planned operating expenses and capital expenditure requirements into the first half of 2028.

About Keros Therapeutics, Inc.

Keros is a clinical-stage biopharmaceutical company focused on developing and commercializing novel therapeutics to treat a wide range of patients with disorders that are linked to dysfunctional signaling of the TGF-ß family of proteins. Keros is a leader in understanding the role of the TGF-ß family of proteins, which are master regulators of the growth, repair and maintenance of a number of tissues, including skeletal muscle, bone, adipose, heart tissue and blood. By leveraging this understanding, Keros has discovered and is developing protein therapeutics that have the potential to provide meaningful and potentially disease-modifying benefit to patients. Keros’ lead product candidate, rinvatercept, is being developed for the treatment of DMD and for the treatment of ALS. Keros’ most advanced product candidate, elritercept, is being developed for the treatment of cytopenias, including anemia and thrombocytopenia, in patients with myelodysplastic syndrome and in patients with myelofibrosis.

Cautionary Note Regarding Forward-Looking Statements

Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. Words such as “anticipates,” “believes,” “continue,” “expects,” “enable,” “potential” and “will” or similar expressions are intended to identify forward-looking statements. Examples of these forward-looking statements include statements concerning: Keros’ expectations regarding its growth, strategy, progress and the design, objectives and timing of its clinical trials for rinvatercept, including its regulatory plans; and Keros’ expected cash runway. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. These risks and uncertainties include, among others: Keros’ limited operating history and historical losses; Keros’ ability to raise additional funding to complete the development and any commercialization of its product candidates; Keros’ dependence on the success of its product candidates, rinvatercept and elritercept; that Keros may be delayed in initiating, enrolling or completing any clinical trials; competition from third parties that are developing products for similar uses; Keros’ ability to obtain, maintain and protect its intellectual property; and Keros’ dependence on third parties in connection with manufacturing, clinical trials and preclinical studies.

These and other risks are described more fully in Keros’ filings with the Securities and Exchange Commission (“SEC”), including the “Risk Factors” section of the Company’s Quarterly Report on Form 10-Q, filed with the SEC on November 5, 2025, and its other documents subsequently filed with or furnished to the SEC, including the Company’s Annual Report on Form 10-K as of and for the year ended December 31, 2025. All forward-looking statements contained in this press release speak only as of the date on which they were made. Except to the extent required by law, Keros undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.

Investor Contact:
Justin Frantz
jfrantz@kerostx.com 
617-221-6042

Media Contact:
Mahmoud Siddig / Adam Pollack / Brooks Hussey
Joele Frank, Wilkinson Brimmer Katcher
(212) 355-4449


KEROS THERAPEUTICS, INC.
Consolidated Statements of Operations
(In thousands, except share and per share data)
(Unaudited)
 
  THREE MONTHS
ENDED DECEMBER 31,
 YEAR ENDED
DECEMBER 31,
   2025   2024   2025   2024 
REVENUE:        
Service and other revenue  385   42   38,706   550 
License revenue     3,000   205,355   3,000 
Total revenue  385   3,042   244,061   3,550 
OPERATING EXPENSES:        
Research and development  (17,912)  (45,631)  (129,643)  (173,629)
General and administrative  (11,743)  (10,665)  (46,849)  (40,754)
Total operating expenses  (29,655)  (56,296)  (176,492)  (214,383)
INCOME (LOSS) FROM OPERATIONS  (29,270)  (53,254)  67,569   (210,833)
OTHER INCOME (EXPENSE), NET:        
Research and development incentive income     1,238      1,238 
Dividend income  4,022   6,519   24,867   23,496 
Other income (expense), net  273   (229)  (539)  (954)
Total other income, net  4,295   7,528   24,328   23,780 
Income (loss) before income taxes  (24,975)  (45,726)  91,897   (187,053)
Income tax provision  1,514   (300)  (4,883)  (300)
Net income (loss) $(23,461) $(46,026) $87,014  $(187,353)
Net income (loss) attributable to common stockholders—basic and diluted $(23,461) $(46,026) $87,014  $(187,353)
         
Weighted-average common stock outstanding—basic  27,198,653   40,337,720   37,221,211   37,437,652 
Weighted-average common stock outstanding—diluted  27,198,653   40,337,720   37,859,106   37,437,652 
         
Net income (loss) per share of common stock — basic $(0.86) $(1.14) $2.34  $(5.00)
Net income (loss) per share of common stock — diluted $(0.86) $(1.14) $2.30  $(5.00)
         


KEROS THERAPEUTICS, INC.
Consolidated Balance Sheets
(In thousands, except share and per share data)
(Unaudited)
 DECEMBER 31,
  2025   2024 
    
ASSETS   
CURRENT ASSETS:   
Cash and cash equivalents$287,415  $559,931 
Accounts receivable 3,567   2,742 
Prepaid expenses and other current assets 22,202   26,220 
Current income tax receivable 2,250    
Total current assets 315,434   588,893 
Operating lease right-of-use assets 16,841   19,251 
Property and equipment, net 4,297   4,237 
Restricted cash 1,449   1,449 
Other long term assets    2,056 
TOTAL ASSETS$338,021  $615,886 
LIABILITIES AND STOCKHOLDERS’ EQUITY   
CURRENT LIABILITIES:   
Accounts payable$1,967  $4,602 
Current portion of operating lease liabilities 2,408   1,978 
Accrued expenses and other current liabilities 16,039   20,870 
Total current liabilities 20,414   27,450 
Operating lease liabilities, net of current portion 14,475   16,883 
Total liabilities 34,889   44,333 
COMMITMENTS AND CONTINGENCIES   
STOCKHOLDERS’ EQUITY:   
Preferred stock, par value of $0.0001 per share; 10,000,000 shares authorized as of December 31, 2025 and December 31, 2024; no shares issued and outstanding     
Series A junior participating preferred stock, par value of $0.0001 per share; 500,000 and no shares authorized as of December 31, 2025 and December 31, 2024, respectively; no shares issued and outstanding     
Common stock, par value of $0.0001 per share; 200,000,000 authorized as of December 31, 2025 and December 31, 2024; 40,670,466 issued and 19,543,706 outstanding as of December 31, 2025 and 40,554,705 shares issued and outstanding as of December 31, 2024 4   4 
Treasury stock, at cost; 21,126,760 and no shares as of December 31, 2025 and December 31, 2024, respectively (384,558)   
Additional paid-in capital 1,169,451   1,140,328 
Accumulated deficit (481,765)  (568,779)
Total stockholders’ equity 303,132   571,553 
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY$338,021  $615,886 



FAQ

When will Keros (KROS) begin the Phase 2 clinical trial of rinvatercept in Duchenne muscular dystrophy?

Keros expects to commence a Phase 2 trial of rinvatercept in DMD in the second quarter of 2026. According to the company, enrollment and operational start are planned for Q2 2026 as part of its 2026 clinical execution priorities.

What drove Keros' (KROS) full-year 2025 net income of $87.0 million?

Keros reported that revenue from a license agreement with Takeda largely produced the $87.0M net income for 2025. According to the company, this license revenue offset R&D and other operating expenses during the year.

How much cash did Keros (KROS) have at year-end 2025 and how long will it last?

Keros had $287.4M in cash and cash equivalents as of December 31, 2025, and expects this to fund operations into the first half of 2028. According to the company, this projection is based on current operating assumptions.

What are Keros' (KROS) plans for rinvatercept in amyotrophic lateral sclerosis (ALS) in 2026?

Keros plans to engage regulators on the design of a Phase 2 rinvatercept trial in ALS in the second half of 2026. According to the company, regulatory interactions and trial design discussions are targeted for H2 2026.

How did Keros (KROS) R&D and G&A expenses change in 2025 compared to 2024?

Research and development expenses decreased to $129.6M in 2025 from $173.6M in 2024, while general and administrative expenses increased to $46.8M from $40.8M. According to the company, R&D declined mainly due to elritercept costs transitioning to Takeda.

Why did Keros (KROS) cash balances fall significantly in 2025?

The company attributed the cash decline to a share repurchase with certain stockholders and a cash tender offer, reducing cash from $559.9M to $287.4M. According to the company, these transactions were primary drivers of the year-over-year cash decrease.
Keros Therapeutics, Inc.

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Biotechnology
Pharmaceutical Preparations
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United States
LEXINGTON