STOCK TITAN

Keros Therapeutics Reports Second Quarter 2026 Financial Results

(Moderate)
(Neutral)
Tags

Keros Therapeutics (Nasdaq: KROS) reported a net loss of $28.7 million for the quarter ended June 30, 2026, compared to a net loss of $30.7 million a year earlier. The company highlighted initiation of a Phase 2 trial of rinvatercept in Duchenne muscular dystrophy (DMD), with initial data expected in the first half of 2027.

Research and development expenses declined to $22.3 million from $43.5 million, and general and administrative expenses fell to $8.6 million from $14.5 million, mainly due to the transition of elritercept expenses to Takeda and a 2025 restructuring. Revenue was $0 in the quarter versus $18.2 million in 2025. Cash and cash equivalents were $257.6 million, and Keros expects this to fund operations into the first half of 2028.

Loading...
Loading translation...

Positive

  • R&D expenses down to $22.3 million from $43.5 million YoY in Q2
  • G&A expenses reduced to $8.6 million from $14.5 million YoY in Q2
  • Cash and cash equivalents of $257.6 million as of June 30, 2026
  • Runway guidance: funding expected into first half of 2028
  • Phase 2 trial initiated for rinvatercept in Duchenne muscular dystrophy

Negative

  • Q2 2026 revenue declined to $0 from $18.2 million in Q2 2025
  • Net loss of $28.7 million in Q2 2026 despite lower operating expenses
  • Cash balance decreased to $257.6 million from $287.4 million since December 31, 2025
  • Six-month 2026 revenue of $0.4 million versus $229.4 million in 2025, reflecting prior one-time license revenue

News Explained

The June 30 balance sheet reports 19,827,188 common shares outstanding versus 19,543,706 at December 31; without issuance terms, the release does not establish whether existing holders’ percentage ownership was diluted.

Market Context

The earnings-tagged record averaged -5.53% across five events, adding historical context to the newl...
Analysis

The earnings-tagged record averaged -5.53% across five events, adding historical context to the newly initiated Phase 2 program and reported results. Recent insider activity was Net Selling; cash runway remains the key watchpoint.

Key Figures

Phase 2 trial initiation: Phase 2 Net loss: $28.7 million R&D expenses: $22.3 million +4 more
7 metrics
Phase 2 trial initiation Phase 2 Rinvatercept in Duchenne muscular dystrophy
Net loss $28.7 million Q2 2026 vs. $30.7 million in Q2 2025
R&D expenses $22.3 million Q2 2026 vs. $43.5 million in Q2 2025
G&A expenses $8.6 million Q2 2026 vs. $14.5 million in Q2 2025
Cash and equivalents $257.6 million As of June 30, 2026 vs. $287.4 million as of December 31, 2025
Operating funding runway First half of 2028 Based on current operating assumptions
Basic loss per share $(1.45) Q2 2026 vs. $(0.76) in Q2 2025

Previous Earnings Reports

5 past events · Latest: May 14 (Negative)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 14 First-quarter earnings Negative -8.3% Net loss replaced prior-year income amid lower license revenue and reduced operating activity.
Mar 04 Fourth-quarter earnings Neutral -15.0% Quarterly loss contrasted with full-year income driven largely by Takeda license revenue.
Nov 05 Third-quarter earnings Positive +3.3% Reduced quarterly loss and lower R&D spending accompanied continued pipeline development.
Aug 06 Second-quarter earnings Positive -7.3% Loss narrowed year over year while KER-065 development and capital-return plans advanced.
May 06 First-quarter earnings Positive -0.4% Net income and cash increased alongside positive Phase 1 program progress.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Earnings-tagged reactions averaged -5.53% and were mixed relative to the reported earnings direction.

Key Terms

tgf-ß, bone mineral density, myelodysplastic syndrome, thrombocytopenia
4 terms
tgf-ß medical
"disorders that are linked to dysfunctional signaling of the transforming growth factor-beta"
Transforming growth factor beta (TGF-ß) is a naturally occurring protein that helps cells talk to each other and controls processes like growth, scarring and immune response. Think of it as a traffic signal for tissues that can either slow down or redirect cell behavior. Investors watch TGF-ß because drugs that change its signals can treat cancer, fibrosis and immune diseases, so changes in research results or regulatory news can strongly affect a biotech’s value.
bone mineral density medical
"increases in muscle mass and bone mineral density, alongside a decrease in fat mass"
A measure of how much mineral — mainly calcium — is packed into a given area of bone, usually obtained from a painless scan; higher values generally mean stronger bones and lower fracture risk. Investors care because changes in this measure are often used as proof that drugs, medical devices, or diagnostics work, so it can drive clinical approval, insurance coverage and sales prospects much like a car’s crash-test rating influences buyer confidence and market demand.
myelodysplastic syndrome medical
"cytopenias, including anemia and thrombocytopenia, in patients with myelodysplastic syndrome"
A bone marrow disorder in which the body’s blood-cell “factory” produces too few or abnormal blood cells, leading to anemia, infections, or bleeding and sometimes progressing to acute leukemia. Investors care because the condition creates clinical and commercial opportunities — drugs, tests and treatments that improve blood counts or delay progression can drive regulatory approvals, patient demand and reimbursement decisions, affecting the value of healthcare and biotech companies.
thrombocytopenia medical
"cytopenias, including anemia and thrombocytopenia"
Thrombocytopenia is a medical condition marked by an abnormally low number of platelets, the blood cells that act like a patching crew to stop bleeding. It matters to investors because it can signal safety risks for drugs or procedures, affect clinical trial outcomes, trigger regulatory scrutiny, lead to additional costs or label changes, and influence a company’s stock if treatments must be halted or modified.

AI-generated analysis. How Rhea-AI works. Not financial advice.

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google

LEXINGTON, Mass., Aug. 03, 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 quarter ended June 30, 2026.

“We are excited to have initiated our Phase 2 clinical trial evaluating the treatment of rinvatercept in patients with Duchenne muscular dystrophy (“DMD”), marking an important milestone in the development of our program,” said Jasbir S. Seehra, Ph.D., President and Chief Executive Officer. “In our Phase 1 clinical trial in healthy volunteers, rinvatercept demonstrated robust pharmacological activity observed through increases in muscle mass and bone mineral density, alongside a decrease in fat mass. We look forward to the progression of the Phase 2 clinical trial, and continue to expect to present initial data in the first half of 2027.”

Second Quarter 2026 Financial Results

Keros reported a net loss of $28.7 million in the second quarter of 2026 as compared to a net loss of $30.7 million in the second quarter of 2025. The decrease of $2.0 million was primarily due to revenue recognized in 2025 related to Keros' license agreement with Takeda and decreased research and development efforts.

Research and development expenses were $22.3 million for the second quarter of 2026 as compared to $43.5 million for the same period in 2025. The decrease of $21.2 million was primarily due to the transition of elritercept-related research and development expenses to Takeda and the corporate restructuring that was completed in 2025.

General and administrative expenses were $8.6 million for the second quarter of 2026 as compared to $14.5 million for the same period in 2025. The decrease of $5.9 million was primarily due to a decrease in professional fees and a decrease in compensation costs in connection with the 2025 corporate restructuring.

Keros’ cash and cash equivalents as of June 30, 2026 was $257.6 million compared to $287.4 million as of December 31, 2025. Based on current operating assumptions, Keros expects that its cash and cash equivalents as of June 30, 2026 will enable Keros to fund its 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 amyotrophic lateral sclerosis. 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 “continue”, “expect”, “plan”, “look forward to”, “will”, “potential” 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; 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 May 14, 2026, and its other documents subsequently filed with or furnished to the SEC. 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

KEROS THERAPEUTICS, INC.
Condensed Consolidated Statements of Operations
(In thousands, except share and per share data)
(Unaudited)
    
 THREE MONTHS
ENDED JUNE 30,
 SIX MONTHS
ENDED JUNE 30,
 2026   2025   2026   2025 
REVENUE:       
Service and other revenue    18,168   367   34,059 
License revenue          195,355 
Total revenue    18,168   367   229,414 
OPERATING EXPENSES:       
Research and development (22,331)  (43,503)  (38,428)  (92,212)
General and administrative (8,606)  (14,482)  (18,753)  (24,979)
Total operating expenses (30,937)  (57,985)  (57,181)  (117,191)
INCOME (LOSS) FROM OPERATIONS (30,937)  (39,817)  (56,814)  112,223 
OTHER INCOME (EXPENSE), NET       
Dividend income 2,287   7,120   4,622   13,912 
Other expense, net (60)  (221)  (226)  (559)
Total other income, net 2,227   6,899   4,396   13,353 
Income (loss) before income taxes (28,710)  (32,918)  (52,418)  125,576 
Income tax (provision) benefit    2,222      (7,821)
Net income (loss)$(28,710) $(30,696) $(52,418) $117,755 
        
Net income (loss) attributable to common stockholders—basic and diluted$(28,710) $(30,696) $(52,418) $117,755 
        
Weighted-average shares of common stock outstanding — basic 19,800,322   40,612,907   19,715,585   40,586,279 
Weighted-average shares of common stock outstanding — diluted 19,800,322   40,612,907   19,715,585   41,153,758 
        
Net income (loss) per share of common stock — basic$(1.45) $(0.76) $(2.66) $2.90 
Net income (loss) per share of common stock — diluted$(1.45) $(0.76) $(2.66) $2.86 
                


KEROS THERAPEUTICS, INC.
Condensed Consolidated Balance Sheets
(In thousands, except share and per share data)
(Unaudited)
    
 JUNE 30,
2026
 DECEMBER 31,
2025
ASSETS   
CURRENT ASSETS:   
Cash and cash equivalents257,606  287,415 
Accounts receivable  3,567 
Prepaid expenses and other current assets7,027  22,202 
Current income tax receivable2,250  2,250 
Total current assets266,883  315,434 
Operating lease right-of-use assets15,553  16,841 
Property and equipment, net3,715  4,297 
Restricted cash1,449  1,449 
TOTAL ASSETS287,600  338,021 
LIABILITIES AND STOCKHOLDERS' EQUITY   
CURRENT LIABILITIES:   
Accounts payable1,816  1,967 
Current portion of operating lease liabilities2,597  2,408 
Accrued expenses and other current liabilities7,740  16,039 
Total current liabilities12,153  20,414 
Operating lease liabilities, net of current portion13,127  14,475 
Total liabilities25,280  34,889 
STOCKHOLDERS' EQUITY:   
Preferred stock, par value of $0.0001 per share; 10,000,000 shares authorized as of June 30, 2026 and December 31, 2025; no shares issued and outstanding   
Series A junior participating preferred stock, par value of $0.0001 per share; 500,000 authorized as of June 30, 2026 and December 31, 2025; no shares issued and outstanding   
Common stock, par value of $0.0001 per share; 200,000,000 shares authorized as of June 30, 2026 and December 31, 2025; 40,953,948 shares issued and 19,827,188 shares outstanding as of June 30, 2026 and 40,670,466 shares issued and 19,543,706 shares outstanding as of December 31, 20254  4 
Treasury stock, at cost; 21,126,760 shares as of June 30, 2026 and December 31, 2025(384,558) (384,558)
Additional paid-in capital1,181,057  1,169,451 
Accumulated deficit(534,183) (481,765)
Total stockholders' equity262,320  303,132 
TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY287,600  338,021 
      

FAQ

How did Keros Therapeutics (KROS) perform financially in Q2 2026?

Keros reported a net loss of $28.7 million in Q2 2026, compared with a $30.7 million net loss in Q2 2025. According to Keros, the quarter had no revenue, versus $18.2 million a year earlier, while operating expenses declined significantly.

What is Keros Therapeutics' cash runway as of June 30, 2026 (KROS)?

Keros held $257.6 million in cash and cash equivalents as of June 30, 2026. According to Keros, based on current operating assumptions, this balance is expected to fund operating expenses and capital expenditure requirements into the first half of 2028.

Why did Keros Therapeutics' revenue drop in Q2 2026 (KROS)?

Keros reported $0 revenue in Q2 2026, compared with $18.2 million in Q2 2025. According to Keros, prior revenue included service and license amounts related to its Takeda agreement, which were not repeated in the current quarter, leading to the decline.

What progress did Keros Therapeutics announce for rinvatercept in DMD in 2026 (KROS)?

Keros initiated a Phase 2 clinical trial of rinvatercept in Duchenne muscular dystrophy during 2026. According to Keros, Phase 1 in healthy volunteers showed pharmacological activity, and the company expects to present initial Phase 2 data in the first half of 2027.

How did Keros Therapeutics reduce expenses in Q2 2026 (KROS)?

Keros cut R&D expenses to $22.3 million from $43.5 million and G&A to $8.6 million from $14.5 million year over year. According to Keros, drivers included transferring elritercept-related R&D to Takeda and a 2025 corporate restructuring.

What are Keros Therapeutics' lead product candidates rinvatercept and elritercept (KROS)?

Rinvatercept is Keros' lead product candidate for Duchenne muscular dystrophy and amyotrophic lateral sclerosis. According to Keros, elritercept is its most advanced candidate, being developed for cytopenias, including anemia and thrombocytopenia, in myelodysplastic syndrome and myelofibrosis.