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Damora Therapeutics Reports First Quarter 2026 Financial Results and Recent Corporate Highlights

Key Takeaway: Damora Therapeutics reported strong first-quarter results for 2026, highlighting significant progress in its mutCALR-targeted therapy pipeline. The company is on track to submit regulatory filings for its lead programs, DMR-001 and DMR-002, in mid-2026. Despite a net loss of $27.8 million, Damora maintains a robust cash position, expected to fund operations into 2029.
Price reaction · baseline $23.09 (2026-05-12 close) · hit pre-market · clean, no other DMRA news in the window
day 0 close · peak
+4.6%

Market Sentiment Analysis

POSITIVE FACTORS

  • DMR-001 shows potentially best-in-class potency and half-life.
  • Strong financial position with $533 million in cash.
  • On track for regulatory submissions for DMR-001 and DMR-002.

CONCERNS & RISKS

  • Net loss increased to $27.8 million compared to $2.5 million last year.
  • R&D expenses rose significantly due to increased preclinical research.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Cash runway
~75 mo
Minimal dilution risk
Lead asset
PAT-1251
Phase 1 · Healthy

Full Press Release Details

– DMR-001 preclinical data showcasing potentially best-in-class potency, half-life and anti-mutCALR activity to be presented at 2026 European Hematology Association Congress –
– On track to submit first regulatory submissions to enable clinical development for DMR-001, an Fc-null anti-mutCALR antibody, and DMR-002, an Fc-enhanced anti-mutCALR antibody,in mid-2026 and second-half 2026, respectively –
– Appointed CEO and key leadership team members to accelerate vision of redefining care for patients with mutCALR-driven myeloproliferative neoplasms –
– Strong financial position with approximately $533 million in cash and cash equivalents as of March 31, 2026, expected to fund operations into 2029 –
BOSTON, May 12, 2026 (GLOBE NEWSWIRE) -- Damora Therapeutics, Inc. (“Damora” or the “Company”) (NASDAQ: DMRA), a biotechnology company working to fundamentally redefine care for patients with blood disorders, today announced its operating and financial results for the quarter ended March 31, 2026, and recent corporate highlights.
“We are pleased with our meaningful progress in advancing our mutant calreticulin (mutCALR)-targeted therapy pipeline, including three highly differentiated assets with distinct mechanisms that uniquely position Damora to drive innovation across all forms of mutCALR-driven disease,” said Jennifer Jarrett, President and Chief Executive Officer of Damora Therapeutics. “Our lead program, DMR-001, remains on track for regulatory submission in mid-2026, and we have designed our first clinical study to generate data beginning in mid-2027 supporting differentiation in both mutCALR-driven essential thrombocythemia (ET) and myelofibrosis (MF), and to enable rapid initiation of Phase 3 development as early as mid-2028. With a strong balance sheet, experienced team and clear development strategy, we are well positioned to maintain or reduce the time to market entry following the current mutCALR leader and deliver a potentially best-in-class treatment to patients.”

Program Updates

Corporate Highlights

Anticipated Milestones

Damora anticipates the following upcoming milestones across its mutCALR programs:

First Quarter 2026 Financial Results

Financial results for the first quarter of 2026 represent the first quarterly results reported for Damora Therapeutics, following the acquisition of rights to the Company’s anti-mutCALR portfolio, appointment of new board and executive leadership, and the renaming of the Company.
Cash Position:Cash and cash equivalents were approximately $532.9 million as of March 31, 2026. The Company anticipates that its cash and cash equivalents will be sufficient to fund operations into 2029.
R&D Expenses:Research and development expenses were $23.8 million for the three months ended March 31, 2026, compared to $0.7 million for the three months ended March 31, 2025. The increase was primarily driven by increased preclinical research, manufacturing and personnel costs, including a non-cash stock-based compensation charge related to a warrant obligation pursuant to the Antibody Discovery and Option Agreement that the Company has with Paragon Therapeutics.
G&A Expenses:General and administrative expenses were $7.0 million for the three months ended March 31, 2026, compared to $1.9 million for the three months ended March 31, 2025. The increase was primarily driven by increased stock-based compensation and personnel costs, along with increased professional fees.

Net Loss:Net loss for the three months ended March 31, 2026, was $27.8 million, compared to $2.5 million for the three months ended March 31, 2025.

About Damora Therapeutics

Damora Therapeutics is an innovative biotechnology company that aims to fundamentally redefine care for people with hematologic disorders. We are advancing a new generation of biologics to treat mutant calreticulin-driven myeloproliferative neoplasms, including essential thrombocythemia and myelofibrosis, where there is significant medical need for disease-modifying treatments. With multiple programs with best-in-class potential on track to enter clinical development in 2026, our goal is to rapidly bring forward optimized therapies with broad mutation coverage and exceptional convenience to dramatically improve patient outcomes. For more information, visitwww.damoratx.comor follow us on LinkedIn.

Forward-Looking Statements

Certain statements in this press release, other than purely historical information, may constitute “forward-looking statements” within the meaning of the federal securities laws, including for purposes of the safe harbor provisions under the United States Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, express or implied statements relating to the Company’s expectations, hopes, beliefs, intentions or strategies regarding the future of its assets, pipeline and business including, without limitation, the timing for regulatory submissions for DMR-001, DMR-002 and DMR-003, the expected timing for Phase 1 data for DMR-001, the expected timing for initiation of Phase 3 development for DMR-001, the Company’s belief that its portfolio of assets have best-in-class potential, and the length of time that the Company believes its existing cash and cash equivalents will fund its operations. In addition, any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking statements. These forward-looking statements are based on current expectations and beliefs concerning future developments and their potential effects. There can be no assurance that future developments affecting the Company will be those that have been anticipated. These forward-looking statements involve a number of risks, uncertainties (some of which are beyond the Company’s control) or other assumptions that may cause actual results or performance to be materially different from those expressed or implied by these forward-looking statements. These risks and uncertainties include, but are not limited to, those uncertainties and factors described under the headings “Risk Factors,” “Cautionary Information Regarding Forward-Looking Statements” or “Cautionary Statement Regarding Forward-Looking Statements” in the Company’s most recent filings with the SEC. Should one or more of these risks or uncertainties materialize, or should any of the Company’s assumptions prove incorrect, actual results may vary in material respects from those projected in these forward-looking statements. Nothing in this press release should be regarded as a representation by any person that the forward-looking statements set forth therein will be achieved or that any of the contemplated results of such forward-looking statements will be achieved. You should not place undue reliance on forward-looking statements in this press release, which speak only as of the date they are made and are qualified in their entirety by reference to the cautionary statements herein. The Company does not undertake or accept any duty to make any updates or revisions to any forward-looking statements.

Investor/Media Contact:

Jim BakerChief Corporate Affairs OfficerDamora Therapeutics
DAMORA THERAPEUTICS, INC.
Condensed Consolidated Balance Sheets
(in thousands, except share and per share amounts)
March 31, December 31,
2026 2025
Assets (unaudited)
Current assets
Cash and cash equivalents $ 532,899 $ 257,624
Prepaid expenses and other current assets 2,509 2,799
Total current assets 535,408 260,423
Other assets, noncurrent 34 104
Total assets $ 535,442 $ 260,527
Liabilities and stockholders’ equity
Current liabilities
Accounts payable $ 819 $ 444
Accrued expenses and other current liabilities 5,997 2,401
Warrant Obligation 4,984
Related party accounts payable and other current liabilities 12,012 17,221
Total current liabilities 23,812 20,066
Other liabilities, noncurrent 27 81
Total liabilities 23,839 20,147
Commitments and contingencies (Note 7)
Mezzanine equity
Preferred stock 1,341 1,341
Stockholders’ equity
Series B non-voting convertible preferred stock 117,621 117,621
Series C non-voting convertible preferred stock 13,490 297,291
Common stock 1
Additional paid-in capital 893,542 310,688
Accumulated deficit (515,146 ) (487,363 )
Accumulated other comprehensive income 754 802
Total stockholders’ equity 511,603 240,380
Total liabilities and stockholders’ equity $ 535,442 $ 260,527
DAMORA THERAPEUTICS, INC.
Consolidated Statements of Operations and Comprehensive Loss
(unaudited, in thousands, except share and per share amounts)
Three Months Ended March 31,
2026 2025
Operating expenses
Research and development $ 23,777 $ 678
General and administrative 7,034 1,921
Total operating expenses 30,811 2,599
Loss from operations (30,811 ) (2,599 )
Other income (expense), net
Interest income, net 3,070 74
Foreign exchange transaction gain (loss), net (6 )
Total other income, net 3,070 68
Loss before income tax expense (27,741 ) (2,531 )
Income tax expense (42 ) (2 )
Net loss $ (27,783 ) $ (2,533 )
Net loss per share, basic and diluted, Series B Preferred Stock $ (353.72 ) $
Weighted-average Series B non-voting convertible preferred stock outstanding,basic and diluted 16,366
Net loss per share, basic and diluted, Series C Preferred Stock $ (33.07 ) $
Weighted-average Series C non-voting convertible preferred stock outstanding,basic and diluted 20,079
Net loss per share, basic and diluted, common stock $ (0.62 ) $ (1.92 )
Weighted-average number of shares used in computing net lossper common share, basic and diluted 34,299,182 1,322,011
Other comprehensive income (loss), net of tax
Currency translation gain (loss) $ (48 ) $ 203
Other comprehensive income (loss), net of tax (48 ) 203
Total comprehensive loss $ (27,831 ) $ (2,330 )

Frequently Asked Questions

What are the key highlights from Damora's Q1 2026 report?

Damora reported progress in its mutCALR-targeted therapies and a strong cash position.

When will Damora submit regulatory filings for its therapies?

Regulatory submissions for DMR-001 and DMR-002 are expected in mid-2026.

What was Damora's net loss for Q1 2026?

The net loss for Q1 2026 was $27.8 million, up from $2.5 million the previous year.

How much cash does Damora have as of March 31, 2026?

Damora has approximately $533 million in cash and cash equivalents.

What is the focus of Damora Therapeutics?

Damora focuses on redefining care for patients with mutCALR-driven blood disorders.

Last updated: May 13, 2026