Damora Therapeutics DMRA
Damora Therapeutics reported a $31.99 million net loss for Q3 2026.
Quarterly report, 8 new risk factors
- Form
- 10-Q
- Filed
- Importance
- Notable
- Accession
- 0001193125-26-447162
- Net loss: $31.99 million for the three months ended Sep 30, 2026
- Diluted EPS: -$0.40 for the three months ended Sep 30, 2026
- Cash and equivalents: $349.66 million at Sep 30, 2026
Written from the 10-Q on EDGAR. Check the filing before you rely on it.
What changed since last quarter
8 new risk factors · 8 removed
Compared with the 10-Q for the period ended Jun 30, 2026.
| This filing | Previous | Change vs prior 10-Q | |
|---|---|---|---|
| Operating income and margin | −$36.86M | −$34.99M | −5.3% |
| Net income | −$31.99M | −$31.17M | −2.6% |
| Operating cash flow | −$17.23M | −$21.87M | +21% |
| Cash | $349.66M | $540.52M | −35% |
New risk factors (8)
- We are substantially dependent on the success of DMR-001, and our ongoing Phase 1/1b clinical trial and any future clinical trial of such product candidates may not be successful.
- Moreover, enrolling patients in clinical trials for MPNs is challenging, as patients with ET or MF will typically first receive the applicable standard of care. Many patients who respond adequately to or tolerate the standard of care therapy (and thus do not enroll in clinical trials) may have disease that would have…
- Currently, many lower-risk ET patients are treated with aspirin alone, which may reduce the number of patients eligible for, or motivated to enroll in, our clinical trials. Higher-risk ET patients carry a greater risk of clotting and bleeding and are generally treated with hydroxyurea, which is not approved for the…
- Results of our clinical trials could reveal a high or unacceptable severity and prevalence of side effects, adverse events or unexpected characteristics. If significant adverse events or other side effects are observed in our ongoing or future clinical trials, we may have difficulty recruiting patients to such…
- Our future growth may depend, in part, on our ability to develop and commercialize our product candidates, if approved, in foreign markets for which we may rely on collaboration with third parties. Recent and ongoing changes in the United States trade policy with foreign countries, including the continued uncertainty…
- and 3 more in the filing
Removed risk factors (8)
- • There is no guarantee that our acquisition of Pre-Acquisition Damora in November 2025 will increase shareholder value.
- There is no guarantee that our acquisition of Pre-Acquisition Damora will increase shareholder value. +1 more paragraph
- Moreover, enrolling patients in clinical trials for cancer therapies is challenging, as cancer patients will first receive the applicable standard of care. Many patients who respond positively to the standard of care therapy (and thus do not enroll in clinical trials) are believed to have tumor types that may have…
- Currently, most ET patients are often treated with aspirin alone. However, the remaining ET patients carry a higher risk of clotting and bleeding and are generally treated with hydroxyurea, which is not approved for the treatment of ET in the United States, anagrelide or interferon.
- Our future growth may depend, in part, on our ability to develop and commercialize our product candidates, if approved, in foreign markets for which we may rely on collaboration with third parties. Recent and ongoing changes in the United States trade policy with foreign countries, including the continued uncertainty…
- and 3 more in the filing
The reading, claim by claim
- • other risks and uncertainties, including those listed under the section titled "Risk Factors."
- For the quarter ended September 30, 2026, Damora Therapeutics, Inc. reported: Net income -$32.0 million.
2 of 2 claims matched the filing text.
From the filing
Item 6.
Item 6.
Exhibits
73
Signatures
75 i
CAUTIONARY NOTE REGARDI NG FORWARD-LOOKING STATEMENTS
This Quarterly Report on Form 10-Q includes "forward-looking statements" within the meaning of Section 27A of the Securities Act of 1933, as amended (the "Securities Act") and Section 21E of the Securities Exchange Act of 1934, as amended (the "Exchange Act"). All statements other than statements of historical fact are "forward-looking statements" for purposes of this Quarterly Report on Form 10-Q. In some cases, you can identify forward-looking statements by terminology such as "may," "could," "will," "would," "should," "expect," "plan," "anticipate," "believe," "estimate," "intend," "predict," "seek," "contemplate," "project," "continue," "potential," "ongoing," "goal," or the negative of these terms or other comparable terminology. These forward-looking statements include, but are not limited to, statements regarding:
• our ability to successfully execute on our strategy for the discovery and development of DMR-001, DMR-002 and DMR-003;
• the success, cost and timing of our planned filing of investigational new drug applications or their equivalents, planned product development activities, and initiation of clinical trials of our current product candidates, including DMR-001, DMR-002, and DMR-003, and any future product candidates;
• our ability to retain the continued service of our directors, officers, key employees and consultants;
• our ability to continue to grow and manage our growth effectively;
• our ability to obtain regulatory approval for our current or future product candidates that we may identify or develop;
• our ability to ensure adequate supply of our current or future product candidates;
• our ability to maintain third-party relationships necessary to conduct our business;
• our ability to establish an adequate safety or efficacy profile for our current or future product candidates that we may pursue;
• the implementation and execution of our strategic plans for our business, our current or future product candidates we may develop and our technology;
• our intellectual property position, including the scope of protection we are able to establish and maintain for intellectual property rights covering our product candidates and technology;
• the rate and degree of market acceptance and clinical utility for our current or future product candidates we may develop;
• our estimates about the size of our market opportunity;
• our estimates of expenses, future revenues, capital requirements and our needs for additional financing;
• our ability to maintain and establish collaborations;
• our financial performance and liquidity;
• developments relating to our competitors and our industry, including the impact of government regulation;
• our ability to retain the continued service of our key professionals and consultants and to identify, hire and retain additional qualified professionals;
• our ability to maintain adequate internal controls over financial reporting;
• the effects of global economic uncertainty and financial market volatility caused by economic effects of volatility in inflation and interest rates, tariffs, geopolitical instability, changes in international trade relationships and conflicts; and
• other risks and uncertainties, including those listed under the section titled "Risk Factors.1"
These statements relate to future events or to our future financial performance and involve known and unknown risks, uncertainties, and other factors that may cause our actual results, performance, or achievements to be materially different from any future results, performance, or achievements expressed or implied by these forward-looking statements. Factors that may cause actual ii results to differ materially from current expectations include, among other things, the reasons described elsewhere in this Quarterly Report on Form 10-Q and those set forth in Part I, Item 1A - "Risk Factors" in our Annual Report on Form 10-K for the fiscal year ended December 31, 2025. Any forward-looking statement in this Quarterly Report on Form 10-Q reflects our current view with respect to future events and is subject to these and other risks, uncertainties, and assumptions relating to our operations, results of operations, industry, and future growth. Given these uncertainties, you should not place undue reliance on these forward-looking statements. Except as required by law, we assume no obligation to update or revise these forward-looking statements for any reason, even if new information becomes available in the future.
This Quarterly Report on Form 10-Q also contains estimates, projections, and other information concerning our industry, our business, and the markets for certain drugs, including data regarding the estimated size of those markets, their projected growth rates, and the incidence of certain medical conditions. Information that is based on estimates, forecasts, projections, or similar methodologies is inherently subject to uncertainties, and actual events or circumstances may differ materially from events and circumstances reflected in this information. Unless otherwise expressly stated, we obtained these industry, business, market, and other data from reports, research surveys, studies, and similar data prepared by third parties, industry, medical and general publications, government data, and similar sources. In some cases, we do not expressly refer to the sources from which these data are derived.
Except where the context otherwise requires, in this Quarterly Report on Form 10-Q, "we," "us," "our," "Damora," and the "Company" refer to Damora Therapeutics, Inc. and, where appropriate, its consolidated subsidiaries.
Trademarks
We have applied for various trademarks that we use in connection with the operation of our business. This Quarterly Report on Form 10-Q includes trademarks, service marks, and trade names owned by us or other companies. All trademarks, service marks, and trade na
Item 1. Finan cial Statements (Unaudited).
Item 1. Finan cial Statements (Unaudited).
DAMORA THERAPEUTICS, INC.
Condensed Consolidated Ba lance Sheets (in thousands, except share and per share amounts)
September 30,
December 31,
2026
2025
Assets (unaudited)
Current assets
Cash and cash equivalents
$
349,656
$
257,624
Marketable securities
178,822
—
Prepaid expenses and other current assets
2,839
2,799
Total current assets
531,317
260,423
Operating lease right-of-use asset
830
68
Other assets, noncurrent
480
36
Total assets
$
532,627
$
260,527
Liabilities and shareholders' equity
Current liabilities
Accounts payable
$
6,084
$
444
Accrued expenses and other current liabilities
12,830
2,401
Paramora warrant obligation
11,862
—
Related party accounts payable and other current liabilities
4,963
17,221
Operating lease liabilities, current
153
—
Total current liabilities
35,892
20,066
Operating lease liabilities, noncurrent
946
53
Other liabilities, noncurrent
28
28
Total liabilities
36,866
20,147
Commitments and contingencies (Note 9)
Mezzanine equity
Preferred shares, par value of $ 0.00001 per share; 10,000,000 shares authorized at September 30, 2026 and December 31, 2025; no shares and 159 shares issued and outstanding as of September 30, 2026 and December 31, 2025
—
1,341
Shareholders' equity
Series B non-voting convertible preferred shares, par value of $ 0.00001 per share;
16,366 shares authorized, issued and outstanding at September 30, 2026 and December 31, 2025
117,621
117,621
Series C non-voting convertible preferred shares, par value of $ 0.00001 per share;
43,882 shares authorized at September 30, 2026 and December 31, 2025; 1,722 and 43,882 shares issued and outstanding as of September 30, 2026 and December 31, 2025, respectively
12,376
297,291
Ordinary shares, par value of $ 0.00001 per share; 500,000,000 shares authorized at September 30, 2026 and 300,000,000 shares authorized at December 31, 2025;
1
—
Additional paid-in capital
944,307
310,688
Accumulated deficit
( 578,311
)
( 487,363
)
Accumulated other comprehensive (loss) income
( 233
)
802
Total shareholders' equity
495,761
239,039
Total liabilities and shareholders' equity
$
532,627
$
260,527
See accompanying notes to the unaudited interim condensed consolidated financial statements.
Damora Therapeutics, Inc.
Condensed Consolidated Statements of Oper ations and Comprehensive Loss (in thousands, except share and per share amounts)
(Unaudited)
Three Months Ended September 30,
Nine Months Ended September 30,
2026
2025
2026
2025
Operating expenses
Research and development
$
25,475
$
1,416
$
74,792
$
3,559
General and administrative
11,388
1,740
27,876
5,617
Total operating expenses
36,863
3,156
102,668
9,176
Loss from operations
( 36,863
)
( 3,156
)
( 102,668
)
( 9,176
)
Other income (expense), net
Gain on sale of IP
750
—
750
—
Interest income, net
4,159
42
11,288
166
Foreign exchange transaction loss, net
( 37
)
( 19
)
( 21
)
( 87
)
Total other income, net
4,872
23
12,017
79
Loss before income tax expense
( 31,991
)
( 3,133
)
( 90,651
)
( 9,097
)
Income tax expense
—
—
( 297
)
( 6
)
)
$
( 3,133
)
$
( 90,948
)
$
( 9,103
)
Net loss per share, basic and diluted, Series B Preferred Shares
$
( 400.40
)
$
—
$
( 1,188.20
)
$
—
Weighted-average Series B non-voting convertible preferred shares outstanding, basic and diluted
16,366
—
16,366
—
Net loss per share, basic and diluted, Series C Preferred Shares
$
( 400.40
)
$
—
$
( 1,188.20
)
$
—
Weighted-average Series C non-voting convertible preferred shares outstanding, basic and diluted
1,722
—
7,888
—
Net loss per share, basic and diluted, ordinary shares
$
( 0.40
)
$
( 2.36
)
$
( 1.19
)
$
( 6.88
)
Weighted-average number of shares used in computing net loss per ordinary share, basic and diluted
61,810,033
1,327,039
52,289,247
1,323,886
Other comprehensive (loss) income, net of tax
Currency translation gain (loss)
$
9
$
14
$
( 61
)
$
726
Unrealized loss on marketable securities, net of tax
( 974
)
-
( 974
)
-
Other comprehensive (loss) income, net of tax
( 965
)
14
( 1,035
)
726
Total comprehensive loss
$
( 32,956
)
$
( 3,119
)
$
( 91,983
)
$
( 8,377
)
See accompanying notes to the unaudited interim condensed consolidated financial statements.
2
Damora Therapeutics, Inc.
Condensed Consolidated Statemen ts of Changes in Shareholders' Equity (in thousands, except share amounts)
(Unaudited)
Mezzanine Equity
Shareholders' Equity
Three Months Ended September 30, 2025
Preferred Shares
Series B
Non-Voting
Convertible Preferred Shares
Series C
Non-Voting
Convertible Preferred Shares
Ordinary Shares
Additional
Paid-In
Accumulated
Accumulated
Other
Comprehensive
Total
Shareholders'
Shares
Amount
Shares
Amount
Shares
Amount
Shares
Amount
Capital
Deficit
Income
Equity
Balance at June 30, 2025
159
$ 1,341
—
$—
—
$—
1,324,560
$—
292,297
$( 283,494 )
$ 809
$ 9,612
Stock-based compensation expense
—
—
—
—
—
—
—
—
164
—
—
164
Issuance of common stock in connection with vesting of restricted stock units
—
—
—
—
—
—
2,652
—
9
—
—
9
Other comprehensive income, net
—
—
—
—
—
—
—
—
—
14
14
Net loss
—
—
—
—
—
—
—
—
—
( 3,133 )
—
( 3,133 )
Balance at September 30, 2025
159
$ 1,341
—
$—
—
$—
1,327,212
$—
$ 292,470
$( 286,627 )
$ 823
$ 6,666
Mezzanine Equity
Shareholders' Equity
Three Months Ended September 30, 2026
Preferred Shares
Series B
Non-Voting
Convertible Preferred Shares
Series C
Non-Voting
Convertible Preferred Shares
Ordinary Shares
Additional
Paid-In
Accumulated
Accumulated
Other
Comprehensive
Total
Shareholders'
Shares
Amount
Shares
Amount
Shares
Amount
Shares
Amount
Capital
Deficit
Income (Loss)
Equity
Balance at June 30, 2026
—
$-
16,366
$ 117,621
1,722
$ 12,376
61,734,601
$ 1
$ 931,649
$( 546,320 )
$ 732
$ 516,059
Share-based compensation expense
—
—
—
—
—
—
—
—
7,541
—
—
7,541
Issuance of ordinary shares in connection with vesting of restricted share units
—
—
—
—
—
—
918
—
—
—
—
—
Exercise of options
—
Similar companies
Companies of similar size in SIC 2834 and related industry codes: the same peer list as the financial tables.
- Synlogic SYBX public float $4M, Jun 30, 2025
- Matinas BioPharma Holdings MTNB public float $5M, Jun 30, 2025
- China Pharma Holdings CPHI public float $4M, Jun 30, 2025
- Soligenix SNGX public float $5M, Jun 30, 2025
- Target Group CBDY public float $5M, Jun 30, 2025
