{"id":962787,"date":"2026-05-14T09:59:38","date_gmt":"2026-05-14T13:59:38","guid":{"rendered":"https:\/\/www.marketnewsdesk.com\/index.php\/keros-therapeutics-reports-recent-first-quarter-2026-financial-results\/"},"modified":"2026-05-14T09:59:38","modified_gmt":"2026-05-14T13:59:38","slug":"keros-therapeutics-reports-recent-first-quarter-2026-financial-results","status":"publish","type":"post","link":"https:\/\/www.marketnewsdesk.com\/index.php\/keros-therapeutics-reports-recent-first-quarter-2026-financial-results\/","title":{"rendered":"Keros Therapeutics Reports Recent First Quarter 2026 Financial Results"},"content":{"rendered":"
\n

LEXINGTON, Mass., May 14, 2026 (GLOBE NEWSWIRE) — Keros Therapeutics, Inc. (\u201cKeros\u201d or the \u201cCompany\u201d) (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 (\u201cTGF-\u00df\u201d) family of proteins, today reported financial results for the quarter ended March 31, 2026.<\/p>\n

\u201cContinuing to progress our pipeline remains our top priority, setting the stage for future catalysts and growth opportunities,\u201d said Jasbir S. Seehra, Ph.D., President and Chief Executive Officer. \u201cIn addition, we are excited that our partner, Takeda Pharmaceuticals U.S.A., Inc. (\u201cTakeda\u201d), plans to advance elritercept into a Phase 3 clinical trial to evaluate elritercept as a treatment of anemia in myelofibrosis, broadening the indication opportunity beyond myelodysplastic syndromes.\u201d<\/p>\n

\n First Quarter 2026 Financial <\/strong>
\n Results<\/strong>\n <\/p>\n

Keros reported a net loss of $23.7 million in the first quarter of 2026 as compared to a net income of $148.5 million in the first quarter of 2025. The decrease of $172.2 million was largely due to revenue recognized in 2025 related to Keros’ license agreement with Takeda and decreased research and development efforts.<\/p>\n

Research and development expenses were $16.1 million for the first quarter of 2026 as compared to $48.7 million for the same period in 2025. The decrease of $32.6 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.<\/p>\n

General and administrative expenses were $10.1 million for the first quarter of 2026 as compared to $10.5 million for the same period in 2025. The decrease of $0.4 million was primarily due to a decrease in compensation costs in connection with the 2025 corporate restructuring.<\/p>\n

Keros\u2019 cash and cash equivalents as of March\u00a031, 2026 was $281.5 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 March\u00a031, 2026 will enable Keros to fund its operating expenses and capital expenditure requirements into the first half of 2028.<\/p>\n

\n About Keros Therapeutics, Inc.<\/strong>\n <\/p>\n

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-\u00df family of proteins. Keros is a leader in understanding the role of the TGF-\u00df 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\u2019 lead product candidate, rinvatercept, is being developed for the treatment of Duchenne muscular dystrophy and for the treatment of amyotrophic lateral sclerosis. Keros\u2019 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.<\/p>\n

\n Cautionary Note Regarding Forward-Looking Statements<\/strong>\n <\/p>\n

Statements contained in this press release regarding matters that are not historical facts are \u201cforward-looking statements\u201d within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. Words such as \u201ccontinue\u201d, \u201cexpect\u201d, \u201cplan\u201d, \u201clook forward to\u201d, \u201cwill\u201d, \u201cpotential\u201d or similar expressions are intended to identify forward-looking statements. Examples of these forward-looking statements include statements concerning: Keros\u2019 expectations regarding its growth, strategy, progress and the design, objectives and timing of its clinical trials for rinvatercept and elritercept; Takeda\u2019s plans to advance elritercept into a Phase 3 clinical trial to evaluate elritercept as a treatment of anemia in myelofibrosis; and Keros\u2019 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\u2019 limited operating history and historical losses; Keros\u2019 ability to raise additional funding to complete the development and any commercialization of its product candidates; Keros\u2019 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\u2019 ability to obtain, maintain and protect its intellectual property; and Keros\u2019 dependence on third parties in connection with manufacturing, clinical trials and preclinical studies.<\/p>\n

These and other risks are described more fully in Keros\u2019 filings with the Securities and Exchange Commission (\u201cSEC\u201d), including the \u201cRisk Factors\u201d section of the Company\u2019s Annual Report on Form 10-K, filed with the SEC on March 4, 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.<\/p>\n

\n Investor Contact:<\/strong>\n <\/p>\n

Justin Frantz
jfrantz@kerostx.com
617-221-6042<\/p>\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
\n KEROS THERAPEUTICS, INC.
Condensed Consolidated Statements of Operations
<\/strong>(In thousands, except share and per share data)
(Unaudited)
<\/strong><\/td>\n<\/tr>\n
\u00a0<\/td>\n<\/tr>\n
\u00a0<\/td>\n\n THREE MONTHS ENDED MARCH 31,<\/strong>\n <\/td>\n<\/tr>\n
\u00a0<\/td>\n\n 2026<\/strong>\n <\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\n 2025<\/strong>\n <\/td>\n\u00a0<\/td>\n<\/tr>\n
REVENUE:<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
Service and other revenue<\/td>\n\u00a0<\/td>\n367<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n15,891<\/td>\n\u00a0<\/td>\n<\/tr>\n
License revenue<\/td>\n\u00a0<\/td>\n\u2014<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n195,355<\/td>\n\u00a0<\/td>\n<\/tr>\n
Total revenue<\/td>\n\u00a0<\/td>\n367<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n211,246<\/td>\n\u00a0<\/td>\n<\/tr>\n
OPERATING EXPENSES:<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
Research and development<\/td>\n\u00a0<\/td>\n(16,097<\/td>\n)<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n(48,709<\/td>\n)<\/td>\n<\/tr>\n
General and administrative<\/td>\n\u00a0<\/td>\n(10,147<\/td>\n)<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n(10,497<\/td>\n)<\/td>\n<\/tr>\n
Total operating expenses<\/td>\n\u00a0<\/td>\n(26,244<\/td>\n)<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n(59,206<\/td>\n)<\/td>\n<\/tr>\n
INCOME (LOSS) FROM OPERATIONS<\/td>\n\u00a0<\/td>\n(25,877<\/td>\n)<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n152,040<\/td>\n\u00a0<\/td>\n<\/tr>\n
OTHER INCOME (EXPENSE), NET<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
Dividend income<\/td>\n\u00a0<\/td>\n2,335<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n6,792<\/td>\n\u00a0<\/td>\n<\/tr>\n
Other expense, net<\/td>\n\u00a0<\/td>\n(166<\/td>\n)<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n(338<\/td>\n)<\/td>\n<\/tr>\n
Total other income, net<\/td>\n\u00a0<\/td>\n2,169<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n6,454<\/td>\n\u00a0<\/td>\n<\/tr>\n
Income (loss) before income taxes<\/td>\n\u00a0<\/td>\n(23,708<\/td>\n)<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n158,494<\/td>\n\u00a0<\/td>\n<\/tr>\n
Income tax provision<\/td>\n\u00a0<\/td>\n\u2014<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n(10,043<\/td>\n)<\/td>\n<\/tr>\n
Net income (loss)<\/td>\n$<\/td>\n(23,708<\/td>\n)<\/td>\n\u00a0<\/td>\n$<\/td>\n148,451<\/td>\n\u00a0<\/td>\n<\/tr>\n
\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
Net income (loss) attributable to common stockholders\u2014basic and diluted<\/td>\n$<\/td>\n(23,708<\/td>\n)<\/td>\n\u00a0<\/td>\n$<\/td>\n148,451<\/td>\n\u00a0<\/td>\n<\/tr>\n
\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
Weighted-average shares of common stock outstanding \u2014 basic<\/td>\n\u00a0<\/td>\n19,629,906<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n40,559,355<\/td>\n\u00a0<\/td>\n<\/tr>\n
Weighted-average shares of common stock outstanding \u2014 diluted<\/td>\n\u00a0<\/td>\n19,629,906<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n41,021,325<\/td>\n\u00a0<\/td>\n<\/tr>\n
\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
Net income (loss) per share of common stock \u2014 basic<\/td>\n$<\/td>\n(1.21<\/td>\n)<\/td>\n\u00a0<\/td>\n$<\/td>\n3.66<\/td>\n\u00a0<\/td>\n<\/tr>\n
Net income (loss) per share of common stock \u2014 diluted<\/td>\n$<\/td>\n(1.21<\/td>\n)<\/td>\n\u00a0<\/td>\n$<\/td>\n3.62<\/td>\n\u00a0<\/td>\n<\/tr>\n
\u00a0<\/td>\n<\/tr>\n<\/table>\n

\n \n <\/p>\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
\n KEROS THERAPEUTICS, INC.
Condensed Consolidated Balance Sheets
<\/strong>(In thousands, except share and per share data)
(Unaudited)
<\/strong><\/td>\n<\/tr>\n
\u00a0<\/td>\n<\/tr>\n
\u00a0<\/td>\n\n MARCH 31,<\/strong>
\n
\n 2026<\/strong>\n <\/td>\n		\u00a0<\/td>\n\n DECEMBER 31,<\/strong>
\n
\n 2025<\/strong>\n <\/td>\n<\/tr>\n
\n ASSETS<\/strong>\n <\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
CURRENT ASSETS:<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
Cash and cash equivalents<\/td>\n281,497<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n287,415<\/td>\n\u00a0<\/td>\n<\/tr>\n
Accounts receivable<\/td>\n400<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n3,567<\/td>\n\u00a0<\/td>\n<\/tr>\n
Prepaid expenses and other current assets<\/td>\n6,530<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n22,202<\/td>\n\u00a0<\/td>\n<\/tr>\n
Current income tax receivable<\/td>\n2,250<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n2,250<\/td>\n\u00a0<\/td>\n<\/tr>\n
Total current assets<\/td>\n290,677<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n315,434<\/td>\n\u00a0<\/td>\n<\/tr>\n
Operating lease right-of-use assets<\/td>\n16,205<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n16,841<\/td>\n\u00a0<\/td>\n<\/tr>\n
Property and equipment, net<\/td>\n3,962<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n4,297<\/td>\n\u00a0<\/td>\n<\/tr>\n
Restricted cash<\/td>\n1,449<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n1,449<\/td>\n\u00a0<\/td>\n<\/tr>\n
TOTAL ASSETS<\/td>\n312,293<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n338,021<\/td>\n\u00a0<\/td>\n<\/tr>\n
\n LIABILITIES AND STOCKHOLDERS’ EQUITY<\/strong>\n <\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
CURRENT LIABILITIES:<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
Accounts payable<\/td>\n1,493<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n1,967<\/td>\n\u00a0<\/td>\n<\/tr>\n
Current portion of operating lease liabilities<\/td>\n2,501<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n2,408<\/td>\n\u00a0<\/td>\n<\/tr>\n
Accrued expenses and other current liabilities<\/td>\n8,859<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n16,039<\/td>\n\u00a0<\/td>\n<\/tr>\n
Total current liabilities<\/td>\n12,853<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n20,414<\/td>\n\u00a0<\/td>\n<\/tr>\n
Operating lease liabilities, net of current portion<\/td>\n13,810<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n14,475<\/td>\n\u00a0<\/td>\n<\/tr>\n
Total liabilities<\/td>\n26,663<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n34,889<\/td>\n\u00a0<\/td>\n<\/tr>\n
STOCKHOLDERS’ EQUITY:<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n<\/tr>\n
Preferred stock, par value of $0.0001 per share; 10,000,000 shares authorized as of March 31, 2026 and December 31, 2025; no shares issued and outstanding<\/td>\n\u2014<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u2014<\/td>\n\u00a0<\/td>\n<\/tr>\n
Series A junior participating preferred stock, par value of $0.0001 per share; 500,000 authorized as of March 31, 2026 and December 31, 2025; no shares issued and outstanding<\/td>\n\u2014<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n\u2014<\/td>\n\u00a0<\/td>\n<\/tr>\n
Common stock, par value of $0.0001 per share; 200,000,000 shares authorized as of March 31, 2026 and December 31, 2025; 40,859,597 shares issued and 19,732,837 shares outstanding as of March 31, 2026 and 40,670,466 shares issued and 19,543,706 shares outstanding as of December 31, 2025<\/td>\n4<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n4<\/td>\n\u00a0<\/td>\n<\/tr>\n
Treasury stock, at cost; 21,126,760 shares as of March 31, 2026 and December 31, 2025<\/td>\n(384,558<\/td>\n)<\/td>\n\u00a0<\/td>\n(384,558<\/td>\n)<\/td>\n<\/tr>\n
Additional paid-in capital<\/td>\n1,175,657<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n1,169,451<\/td>\n\u00a0<\/td>\n<\/tr>\n
Accumulated deficit<\/td>\n(505,473<\/td>\n)<\/td>\n\u00a0<\/td>\n(481,765<\/td>\n)<\/td>\n<\/tr>\n
Total stockholders’ equity<\/td>\n285,630<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n303,132<\/td>\n\u00a0<\/td>\n<\/tr>\n
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY<\/td>\n312,293<\/td>\n\u00a0<\/td>\n\u00a0<\/td>\n338,021<\/td>\n\u00a0<\/td>\n<\/tr>\n<\/table>\n

\"\"
\n
\n \"\"\n <\/div>\n

<\/div>\n","protected":false},"excerpt":{"rendered":"

LEXINGTON, Mass., May 14, 2026 (GLOBE NEWSWIRE) — Keros Therapeutics, Inc. (\u201cKeros\u201d or the \u201cCompany\u201d) (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 (\u201cTGF-\u00df\u201d) family of proteins, today reported financial results for the quarter ended March 31, 2026. \u201cContinuing to progress our pipeline remains our top priority, setting the stage for future catalysts and growth opportunities,\u201d said Jasbir S. Seehra, Ph.D., President and Chief Executive Officer. \u201cIn addition, we are excited that our partner, Takeda Pharmaceuticals U.S.A., Inc. (\u201cTakeda\u201d), plans to advance elritercept into a Phase 3 clinical trial to evaluate elritercept as a treatment … <\/p>\n

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(\u201cKeros\u201d or the \u201cCompany\u201d) (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 (\u201cTGF-\u00df\u201d) family of proteins, today reported financial results for the quarter ended March 31, 2026. \u201cContinuing to progress our pipeline remains our top priority, setting the stage for future catalysts and growth opportunities,\u201d said Jasbir S. Seehra, Ph.D., President and Chief Executive Officer. \u201cIn addition, we are excited that our partner, Takeda Pharmaceuticals U.S.A., Inc. 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(\u201cKeros\u201d or the \u201cCompany\u201d) (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 (\u201cTGF-\u00df\u201d) family of proteins, today reported financial results for the quarter ended March 31, 2026. \u201cContinuing to progress our pipeline remains our top priority, setting the stage for future catalysts and growth opportunities,\u201d said Jasbir S. Seehra, Ph.D., President and Chief Executive Officer. \u201cIn addition, we are excited that our partner, Takeda Pharmaceuticals U.S.A., Inc. 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