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Keros Therapeutics Reports Second Quarter 2025 Financial Results

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Keros Therapeutics (NASDAQ: KROS) reported its Q2 2025 financial results, marking significant developments following a comprehensive strategic review. The company posted a net loss of $30.7 million, an improvement from the $45.3 million loss in Q2 2024. Key financial metrics include R&D expenses of $43.5 million and cash position of $690.2 million.

The company plans to return $375 million to stockholders while maintaining sufficient capital to fund operations into first half of 2028. Keros is advancing its pipeline, particularly KER-065, with plans to initiate a Phase 2 trial for Duchenne muscular dystrophy in Q1 2026. The company's improved financial position was supported by revenue from its license agreement with Takeda Pharmaceuticals.

Keros Therapeutics (NASDAQ: KROS) ha comunicato i risultati finanziari del secondo trimestre 2025, segnando sviluppi significativi dopo una revisione strategica completa. La societ脿 ha registrato una perdita netta di 30,7 milioni di dollari, migliorando rispetto alla perdita di 45,3 milioni di dollari del secondo trimestre 2024. I principali indicatori finanziari includono spese di R&S per 43,5 milioni di dollari e una posizione di cassa di 690,2 milioni di dollari.

L'azienda prevede di restituire 375 milioni di dollari agli azionisti, mantenendo al contempo capitale sufficiente per finanziare le operazioni fino alla prima met脿 del 2028. Keros sta portando avanti il suo portafoglio di prodotti, in particolare KER-065, con l'intenzione di avviare uno studio di Fase 2 per la distrofia muscolare di Duchenne nel primo trimestre 2026. La posizione finanziaria migliorata 猫 stata sostenuta dai ricavi derivanti dall'accordo di licenza con Takeda Pharmaceuticals.

Keros Therapeutics (NASDAQ: KROS) inform贸 sus resultados financieros del segundo trimestre de 2025, marcando desarrollos significativos tras una revisi贸n estrat茅gica exhaustiva. La compa帽铆a report贸 una p茅rdida neta de 30,7 millones de d贸lares, mejorando frente a la p茅rdida de 45,3 millones en el segundo trimestre de 2024. Los principales indicadores financieros incluyen gastos en I+D de 43,5 millones de d贸lares y una posici贸n de efectivo de 690,2 millones de d贸lares.

La empresa planea devolver 375 millones de d贸lares a los accionistas, manteniendo suficiente capital para financiar las operaciones hasta la primera mitad de 2028. Keros est谩 avanzando en su cartera, especialmente con KER-065, y tiene previsto iniciar un ensayo de Fase 2 para la distrofia muscular de Duchenne en el primer trimestre de 2026. La mejor posici贸n financiera de la compa帽铆a se apoy贸 en ingresos provenientes de su acuerdo de licencia con Takeda Pharmaceuticals.

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須岇偓電� 欤检<霌れ棎瓴� 3鞏� 7,500毵� 雼煬毳� 頇橃洂頃� 瓿勴殟鞚措┌, 2028雲� 靸侂皹旮瓣箤歆 鞖挫榿 鞛愱笀鞚� 於╇秳頌� 鞙犾頃� 鞓堨爼鞛呺媹雼�. Keros電� 韸鬼瀳 KER-065毳� 欷戩嫭鞙茧 韺岇澊頂勲澕鞚胳潉 歆勳爠鞁滍偆瓿� 鞛堨溂氅�, 2026雲� 1攵勱赴鞐� 霋れ墧 攴检湣鞙勳稌歃濎棎 雽頃� 2靸� 鞛勳儊鞚� 鞁滌瀾頃� 瓿勴殟鞛呺媹雼�. 須岇偓鞚� 臧滌劆霅� 鞛 靸來儨電� Takeda Pharmaceuticals鞕鞚� 霛检澊靹犾姢 瓿勳暯鞐愳劀 氚滌儩頃� 靾橃澋鞐� 頌橃瀰鞚 氚� 韥诫媹雼�.

Keros Therapeutics (NASDAQ: KROS) a publi茅 ses r茅sultats financiers du deuxi猫me trimestre 2025, marquant des avanc茅es significatives apr猫s une r茅vision strat茅gique approfondie. La soci茅t茅 a enregistr茅 une perte nette de 30,7 millions de dollars, une am茅lioration par rapport 脿 la perte de 45,3 millions au deuxi猫me trimestre 2024. Les principaux indicateurs financiers comprennent des d茅penses de R&D de 43,5 millions de dollars et une tr茅sorerie de 690,2 millions de dollars.

L'entreprise pr茅voit de reverser 375 millions de dollars aux actionnaires tout en conservant un capital suffisant pour financer ses op茅rations jusqu'au premier semestre 2028. Keros fait progresser son portefeuille, notamment KER-065, avec l'intention de lancer un essai de phase 2 pour la dystrophie musculaire de Duchenne au premier trimestre 2026. La meilleure situation financi猫re de la soci茅t茅 a 茅t茅 soutenue par les revenus issus de son accord de licence avec Takeda Pharmaceuticals.

Keros Therapeutics (NASDAQ: KROS) ver枚ffentlichte seine Finanzergebnisse f眉r das zweite Quartal 2025 und verzeichnete bedeutende Entwicklungen nach einer umfassenden strategischen 脺berpr眉fung. Das Unternehmen meldete einen Nettoverlust von 30,7 Millionen US-Dollar, eine Verbesserung gegen眉ber dem Verlust von 45,3 Millionen US-Dollar im zweiten Quartal 2024. Wichtige finanzielle Kennzahlen umfassen F&E-Ausgaben von 43,5 Millionen US-Dollar und eine Cash-Position von 690,2 Millionen US-Dollar.

Das Unternehmen plant, 375 Millionen US-Dollar an die Aktion盲re zur眉ckzugeben und dabei ausreichend Kapital f眉r die Finanzierung der Gesch盲ftst盲tigkeit bis zur ersten H盲lfte 2028 zu behalten. Keros treibt seine Produktpipeline voran, insbesondere KER-065, mit Pl盲nen, im ersten Quartal 2026 eine Phase-2-Studie zur Duchenne-Muskeldystrophie zu starten. Die verbesserte finanzielle Lage des Unternehmens wurde durch Einnahmen aus der Lizenzvereinbarung mit Takeda Pharmaceuticals gest眉tzt.

Positive
  • Net loss decreased by $14.6 million year-over-year to $30.7 million
  • Strong cash position of $690.2 million, up from $559.9 million at end of 2024
  • Planned return of $375 million to stockholders while maintaining operations through 2028
  • Strategic partnership revenue from Takeda Pharmaceuticals license agreement
Negative
  • R&D expenses increased by $3.0 million to $43.5 million
  • General and administrative expenses rose by $4.5 million to $14.5 million

Insights

Keros Therapeutics improved financial position with reduced losses, plans to return $375M to shareholders while maintaining strong cash runway into 2028.

Keros Therapeutics' Q2 2025 results show notable financial improvement with net losses decreasing by $14.6 million year-over-year to $30.7 million. This reduction stems primarily from revenue recognition from their Takeda partnership, which offset increased operational costs. The company has strategically increased R&D investments by $3 million to $43.5 million, demonstrating continued commitment to pipeline advancement, particularly their lead asset KER-065 for Duchenne muscular dystrophy.

The most significant development is Keros' substantial cash position of $690.2 million, up from $559.9 million at the end of 2024. This impressive 23% increase in cash reserves provides exceptional financial flexibility. Management's decision to return $375 million to shareholders while still maintaining a cash runway into H1 2028 reflects strong financial health and confidence in capital efficiency.

The company's G&A expenses increased by $4.5 million to $14.5 million, representing a 45% jump that outpaces R&D growth. While this warrants monitoring, the completed strategic review suggests potential reorganization to optimize operational structure. With clinical milestones advancing and a reinforced balance sheet, Keros has positioned itself with approximately three years of operational runway even after the substantial capital return to shareholders.

LEXINGTON, Mass., Aug. 06, 2025 (GLOBE NEWSWIRE) -- Keros Therapeutics, Inc. (鈥淜eros鈥� or the 鈥淐ompany鈥�) (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 (鈥淭GF-脽鈥�) family of proteins, today reported financial results for the quarter ended June 30, 2025.

鈥淭he second quarter marked an important point for Keros, as Keros鈥� Board of Directors (the 鈥淏oard鈥�) completed its comprehensive strategic review,鈥� said Jasbir S. Seehra, Ph.D., Chair and Chief Executive Officer. 鈥淔ollowing the review, our focus remains on creating long-term value through advancing the development of our pipeline of novel therapeutics, including our lead asset, KER-065, which the team is progressing towards initiation of a Phase 2 clinical trial in patients with Duchenne muscular dystrophy in the first quarter of 2026.鈥�

Second Quarter 2025 Financial Results

Keros reported a net loss of $30.7 million in the second quarter of 2025 as compared to a net loss of $45.3 million in the second quarter of 2024. The decrease of $14.6 million was largely due to revenue recognized related to Keros鈥� license agreement with Takeda Pharmaceuticals U.S.A., Inc., partially offset by increased research and development efforts as well as additional investments to support the achievement of Keros鈥� clinical and corporate goals.

Research and development expenses were $43.5 million for the second quarter of 2025 as compared to $40.5 million for the same period in 2024. The increase of $3.0 million was primarily due to additional research and development efforts.

General and administrative expenses were $14.5 million for the second quarter of 2025 as compared to $10.0 million for the same period in 2024. The increase of $4.5 million was primarily due to an increase in other external expenses.

Keros鈥� cash and cash equivalents as of June听30, 2025 was $690.2 million compared to $559.9 million as of December 31, 2024. Based on current operating assumptions, Keros expects that its cash and cash equivalents as of June听30, 2025, less $375.0 million of excess capital that the Board has determined to return to stockholders, 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-脽 family of proteins. Keros is a leader in understanding the role of the TGF-脽 family of proteins, which are master regulators of the growth, repair and maintenance of a number of tissues, including blood, bone, skeletal muscle, adipose and heart tissue. 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鈥� lead product candidate, KER-065, is being developed for the treatment of neuromuscular diseases, with an initial focus on Duchenne muscular dystrophy. Keros鈥� 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 鈥渇orward-looking statements鈥� within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. Words such as 鈥渆nable,鈥� 鈥渆xpects鈥� and 鈥渨ill鈥� or similar expressions are intended to identify forward-looking statements. Examples of these forward-looking statements include statements concerning: Keros鈥� expectations regarding its strategy, progress and timing of its clinical trials for KER-065; Keros鈥� ability to create long-term value through advancing the development of its pipeline of novel therapeutics; the expected capital return; and Keros鈥� 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鈥� limited operating history and historical losses; Keros鈥� ability to raise additional funding to complete the development and any commercialization of its product candidates; Keros鈥� dependence on the success of its product candidates, KER-065 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鈥� ability to obtain, maintain and protect its intellectual property; and Keros鈥� dependence on third parties in connection with manufacturing, clinical trials and preclinical studies.

These and other risks are described more fully in Keros鈥� filings with the Securities and Exchange Commission (鈥淪EC鈥�), including the 鈥淩isk Factors鈥� section of the Company鈥檚 Quarterly Report on Form 10-Q, filed with the SEC on May 6, 2025, 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.

Contacts

Investor Contact:
Justin Frantz
[email protected]
617-221-6042

Media Contact:
Mahmoud Siddig / Adam Pollack / Viveca Tress
Joele Frank, Wilkinson Brimmer Katcher
212-355-4449

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,
2025202420252024
REVENUE:
Service and other revenue18,1683734,059120
License revenue鈥�鈥�195,355鈥�
Total revenue18,16837229,414120
OPERATING EXPENSES:
Research and development(43,503)(40,515)(92,212)(78,773)
General and administrative(14,482)(9,961)(24,979)(20,269)
Total operating expenses(57,985)(50,476)(117,191)(99,042)
INCOME (LOSS) FROM OPERATIONS(39,817)(50,439)112,223(98,922)
OTHER INCOME (EXPENSE), NET
Dividend income7,1205,37813,91211,184
Other expense, net(221)(196)(559)(633)
Total other income, net6,8995,18213,35310,551
Income (loss) before income taxes(32,918)(45,257)125,576(88,371)
Income tax (provision) benefit2,222鈥�(7,821)鈥�
Net income (loss)$(30,696)$(45,257)$117,755$(88,371)
Net income (loss) attributable to common stockholders 鈥� basic and diluted$(30,696)$(45,257)$117,755$(88,371)
Weighted-average shares of common stock outstanding 鈥� basic40,612,90736,103,18740,586,27935,894,305
Weighted-average shares of common stock outstanding 鈥� diluted40,612,90736,103,18741,153,75835,894,305
Net income (loss) per share of common stock 鈥� basic$(0.76)$(1.25)$2.90$(2.46)
Net income (loss) per share of common stock 鈥� diluted$(0.76)$(1.25)$2.86$(2.46)


KEROS THERAPEUTICS, INC.
Condensed Consolidated Balance Sheets
(In thousands, except share and per share data)
(Unaudited)
JUNE 30,
2025
DECEMBER 31,
2024
ASSETS
CURRENT ASSETS:
Cash and cash equivalents690,215559,931
Accounts receivable15,8162,742
Prepaid expenses and other current assets26,77726,220
Total current assets732,808588,893
Operating lease right-of-use assets18,07219,251
Property and equipment, net4,8364,237
Restricted cash1,4491,449
Other long-term assets鈥�2,056
TOTAL ASSETS757,165615,886

LIABILITIES AND STOCKHOLDERS' EQUITY
CURRENT LIABILITIES:
Accounts payable5,2674,602
Current portion of operating lease liabilities2,2301,978
Accrued expenses and other current liabilities19,96420,870
Deferred revenue925鈥�
Current tax liability6,321鈥�
Total current liabilities34,70727,450
Operating lease liabilities, net of current portion15,72416,883
Total liabilities50,43144,333
STOCKHOLDERS' EQUITY:
Preferred stock, par value of $0.0001 per share; 10,000,000 shares authorized as of June 30, 2025 and December 31, 2024; no shares issued and outstanding鈥�鈥�
Series A junior participating preferred stock, par value of $0.0001 per share; 500,000 and no shares authorized as of June 30, 2025 and December 31, 2024, respectively; no shares issued and outstanding
Common stock, par value of $0.0001 per share; 200,000,000 shares authorized as of June 30, 2025 and December 31, 2024; 40,615,414 and 40,554,705 shares issued and outstanding as of June 30, 2025 and December 31, 2024, respectively44
Additional paid-in capital1,157,7541,140,328
Accumulated deficit(451,024)(568,779)
Total stockholders' equity706,734571,553
TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY757,165615,886

FAQ

What were Keros Therapeutics (KROS) Q2 2025 financial results?

Keros reported a net loss of $30.7 million, improved from $45.3 million loss in Q2 2024, with R&D expenses of $43.5 million and cash position of $690.2 million.

How much cash does Keros Therapeutics (KROS) plan to return to shareholders?

Keros plans to return $375 million of excess capital to stockholders while maintaining sufficient funds to operate into first half of 2028.

When will Keros Therapeutics start the Phase 2 trial for KER-065 in Duchenne muscular dystrophy?

Keros plans to initiate the Phase 2 clinical trial for KER-065 in patients with Duchenne muscular dystrophy in the first quarter of 2026.

What is Keros Therapeutics' cash runway?

Based on current operating assumptions, Keros expects its cash position will fund operations into the first half of 2028, after returning $375 million to stockholders.

How did Keros Therapeutics' operating expenses change in Q2 2025?

R&D expenses increased by $3.0 million to $43.5 million, and G&A expenses rose by $4.5 million to $14.5 million compared to Q2 2024.
Keros Therapeutics, Inc.

NASDAQ:KROS

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584.46M
38.64M
2.31%
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12.43%
Biotechnology
Pharmaceutical Preparations
United States
LEXINGTON