Dogwood Therapeutics Q3 loss narrows to $4.88M
The company also reported a fully recruited 95-patient extension study and a closed $5 million private placement.
Sentiment and the balance of points
Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.
Rhea-AI Filing Summary
Dogwood Therapeutics, Inc. reported a third-quarter net loss attributable to common stockholders of $4,882,942, compared with $15,744,616 a year earlier. Revenue was $100,000, compared with no revenue in the third quarter of 2025, reflecting the first payment under the PRIDCor License Agreement. CVR expense was $88,104. Research and development expenses were $3,352,977, compared with $14,521,342; the company attributed the decrease primarily to the prior-year $12.0 million Serpin Licensing Agreement IPR&D expense. General and administrative expenses were $1,576,219, compared with $1,287,783. Cash and cash equivalents were $4,948,266 as of September 30, 2026, versus $6,524,744 as of December 31, 2025.
Dogwood completed the Halneuron Phase 2b trial in chemotherapy-induced neuropathy, with top-line results to be announced in November 2026. Its Phase 2b long-term extension study was fully recruited, with 95 patients enrolled to assess pain reduction over three months of treatment. The company also closed a $5 million private placement with Sealbond Limited, a subsidiary of CK Life Sciences Int’l. (Holdings) Inc., to advance Phase 3 preparatory activities.
How this balance works
Rhea-AI gives every point it takes from this document a weight. Minor counts 1, Moderate 3 and Major 9, so one Major point outweighs several Minor ones. The bar adds up the weights on each side, and when neither side holds more than 65% of the total the balance reads Mixed.
It reads the document as published, with the same rules for every company, and it does not look at what the market expected or at how the stock traded, so a point can be objectively good on a day the stock falls.
Rhea-AI Sentiment measures something else, the tone of the wording.
Positive
- Moderate pointQuarterly common-stockholder loss narrowed to $4,882,942 from $15,744,616.
Negative
- None.
Filing Explained
For the third quarter, Dogwood recognized
8-K Event Classification
Key Figures
Key Terms
contingent value rights financial
acquired in-process research and development financial
Chemotherapy Induced Neuropathy medical
LRP1 agonist medical
Earnings Snapshot
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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM
CURRENT REPORT
PURSUANT TO SECTION 13 OR 15(d) OF THE
SECURITIES EXCHANGE ACT OF 1934
Date of Report (Date of earliest event reported):
(Exact Name of Registrant as Specified in Charter)
(Address of principal executive offices) | (Zip Code) |
Registrant’s telephone number, including area code: (
(Former name or former address, if changed since last report): Not Applicable
Securities registered pursuant to Section 12(b) of the Act:
Title of each class | Trading Symbol(s) | Name of each exchange on which registered |
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) | |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) | |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) | |
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging growth company
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Item 2.02 Results of Operations and Financial Condition.
On November 5, 2026, Dogwood Therapeutics, Inc. (the “Company”) issued a press release announcing the results of operations for the third quarter ended September 30, 2026. A copy of the press release is included as Exhibit 99.1 to this Current Report on Form 8-K and is hereby incorporated by reference into this Item 2.02.
The information provided pursuant to this Item 2.02, including Exhibit 99.1, is being furnished and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934 (the “Exchange Act”) or otherwise subject to the liabilities under that Section and shall not be deemed to be incorporated by reference into any filing of the Company under the Securities Act of 1933 or the Exchange Act.
Item 9.01 Financial Statements and Exhibits.
(d)Exhibits.
Exhibit Number | | Description |
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SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
| DOGWOOD THERAPEUTICS, INC. | |
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| By: | /s/ Angela Walsh |
| Name: | Angela Walsh |
Title: | Chief Financial Officer, Corporate Secretary and Treasurer | |
November 5, 2026 | ||
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Exhibit 99.1
Dogwood Therapeutics Announces Third Quarter 2026 Financial Results
- Completed the Halneuron® Phase 2b trial in Chemotherapy Induced Neuropathy, top-line results to be announced in November 2026 -
- Phase 2b Long-Term Extension Study fully recruited, 95 patients enrolled, assessing Halneuron® reduction in pain over three months of treatment with Halneuron® -
- Closed $5M Private Placement with Sealbond Limited, a subsidiary of CK Life Sciences Int’l., (Holdings) Inc., to Advance Phase 3 Preparatory Activities -
ALPHARETTA, Ga., November 5, 2026 -- Dogwood Therapeutics, Inc. (Nasdaq: DWTX) (“Dogwood” or the “Company”), a company that focuses on developing first-in-class, new non-opioid medicines to treat pain and neuropathy, today announced financial results for the third quarter ended September 30, 2026.
“Tens of millions of cancer patients worldwide previously treated with chemotherapy suffer from long-term, moderate-to-severe neuropathic pain (“CINP”),” said Greg Duncan, Chief Executive Officer of Dogwood Therapeutics. “Despite the massive unmet medical need associated with significant pain from ‘off-target’ chemotherapy-related nerve damage, there are no FDA approved medicines to treat CINP. Halneuron® has demonstrated statistically and/or clinically significant and durable pain reduction in cancer and CINP clinical trials to date. With results from the recently completed Phase 2b CINP study to be reported in November, we believe that if successful, Halneuron® could represent the first new therapeutic agent for millions of CINP patients in the US and tens of millions of CINP patients across the globe.”
Key Highlights
| • | The Company completed its Halneuron® Phase 2b Chemotherapy Induced Neuropathic Pain (“CINP”) study, enrolling 239 patients. Top-line results are expected to be announced in November 2026. |
| • | Dogwood has fully enrolled 95 patients in its Phase 2b long-term extension study to assess Halneuron®’s reduction in pain over three months of treatment. Patients who completed the ongoing Halneuron® 4-week CINP Phase 2b study were eligible to enroll in the 12-week open-label follow-on trial. The long-term extension study is expected to be completed in early 2027. |
| • | The Company closed a $5 million private placement with Sealbond Limited, its largest shareholder, and a subsidiary of CK Life Sciences Int’l., (Holdings) Inc. to advance Phase 3 preparatory activities for Halneuron® and for working capital and general corporate purposes. |
| • | Cash on hand of $4.9 million along with the private placement of $5 million provides operational runway through the first quarter of 2027. |
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Third Quarter 2026 Financial Results
Revenue and CVR expense for the third quarter of 2026 were $0.1 million and $0.1 million, respectively, compared to no revenue and no CVR expense in the third quarter of 2025. In the third quarter of 2026, the Company received and recognized $0.1 million in licensing revenue for its first payment under the PRIDCor License Agreement and recognized cost of goods sold of $0.1 million related to the corresponding payment to its CVR Holders under the CVR Agreement.
Research and development expenses for the third quarter of 2026 were $3.3 million, compared to $14.5 million for the third quarter of 2025. The $11.2 million decrease year over year primarily related to a decrease in acquired in-process research and development (“IPR&D”) expenses of $12.0 million related to the Serpin Licensing Agreement that took place in the third quarter of 2025 offset by an increase in the Halneuron® Phase 2b CINP study costs of $0.5 million, an increase in drug development and manufacturing costs of $0.2 million and an increase in salaries and related personnel costs of $0.1 million.
General and administrative expenses for the third quarter of 2026 were $1.6 million, compared to $1.3 million for the third quarter of 2025. The $0.3 million increase year over year was primarily due to increases in salaries and related personnel costs of $0.4 million offset by a decrease in legal and accounting fees of $0.1 million.
Net loss attributable to common stockholders for the third quarter of 2026 was $4.9 million, or $0.14 basic and diluted net loss per share, compared to a net loss attributable to common stockholders of $15.7 million, or $8.20 basic and diluted net loss per share, for the third quarter of 2025.
About Dogwood Therapeutics
Dogwood Therapeutics (Nasdaq: DWTX) is a development-stage biopharmaceutical company focused on developing first-in-class, non-opioid medicines to treat pain and neuropathic disorders. Dogwood’s research pipeline includes two first-in-class development candidates, Halneuron® and SP16 IV.
Our lead product candidate, Halneuron®, is in Phase 2b development to treat pain conditions including the neuropathic pain associated with chemotherapy treatment. Halneuron® has been granted fast track designation from the FDA for the treatment of CINP. Halneuron® is a non-opioid, NaV 1.7 analgesic which is a highly specific voltage-gated sodium channel modulator, a mechanism known to be effective for reducing pain transmission. In clinical studies, Halneuron® treatment has demonstrated pain reduction in pain related to general cancer and in pain related to chronic CINP.
SP16 IV is a low-density lipoprotein receptor related protein-1 agonist (“LRP1”) with potential to treat neuropathy and prevent or repair nerve damage following chemotherapy. SP16 acts as an LRP1 agonist that in turn provides alpha-1-antitrypsin-like activity. Consistent with alpha-1-antitrypsin anti-inflammatory and immunomodulatory actions, SP16 preclinically demonstrated anti-inflammatory (analgesic) action via potential reductions in IL-6, IL-8, IL1B and TNF-alpha levels, as well as potential to repair damaged tissue via increases in pAKT and pERK that regulate fundamental processes like growth, proliferation and survival. The forthcoming SP16 IV Phase 1b CIPN trial is fully funded by the National Cancer Institute.
Dogwood Therapeutics’ largest shareholder is a member of CK Life Sciences Int’l., (Holdings) Inc., which is listed on the Hong Kong Stock Exchange (Stock code: 0775).
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For more information, please visit www.dwtx.com.
Development and Commercialization Partnership Payments
To the extent that any payment to Dogwood resulting from the development and commercialization partnership constitutes either an “Upfront Payment” or a “Milestone Payment” under the terms and conditions applicable to the contingent value rights (“CVRs”) issued by Dogwood on October 17, 2024, Dogwood will cause any required amounts to be delivered to the rights agent for further payment to holders of the CVRs.
Forward-Looking Statements:
Statements in this press release contain “forward-looking statements,” within the meaning of the U.S. Private Securities Litigation Reform Act of 1995, that are subject to substantial risks and uncertainties. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as “anticipate,” “believe,” “contemplate,” “could,” “estimate,” “expect,” “intend,” “seek,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “suggest,” “target,” “aim,” “should,” "will,” “would,” or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements are based on Dogwood’s current expectations and are subject to inherent uncertainties, risks and assumptions that are difficult to predict, including risks related to the completion, timing and results of current and future clinical studies relating to Dogwood’s product candidates. Further, certain forward-looking statements are based on assumptions as to future events that may not prove to be accurate. These and other risks and uncertainties are described more fully in the section titled “Risk Factors” in the most recently filed Annual Report on Form 10-K, which has been filed with the Securities and Exchange Commission (the “SEC”). Forward-looking statements contained in this announcement are made as of this date, and Dogwood undertakes no duty to update such information except as required under applicable law.
Investor Relations:
Dan Ferry
Managing Director
LifeSci Advisors, LLC
daniel@lifesciadvisors.com
-Financial Tables Follow-
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DOGWOOD THERAPEUTICS
Selected Financial Data
(unaudited)
Condensed Consolidated Statements of Operations Data | | Three Months Ended September 30, | | | Nine Months Ended September 30, | | |||||||||||
| | 2026 | | | 2025 | | | 2026 | | | 2025 | | |||||
Licensing revenue | | $ | 100,000 | | | $ | — | | | $ | 100,000 | | | $ | — | | |
CVR expense | | | 88,104 | | | | — | | | | 88,104 | | | | — | | |
Gross profit | | | 11,896 | | | | — | | | | 11,896 | | | | — | | |
Operating expenses: | | | | | | | | | | | | | | | | | |
Research and development | | | 3,352,977 | | | | 14,521,342 | | | | 9,269,275 | | | | 19,528,283 | | |
General and administrative | | | 1,576,219 | | | | 1,287,783 | | | | 5,608,915 | | | | 4,633,883 | | |
IPR&D impairment | | | — | | | | — | | | | 9,190,897 | | | | — | | |
Total operating expenses | | | 4,929,196 | | | | 15,809,125 | | | | 24,069,087 | | | | 24,162,166 | | |
Loss from operations | | | (4,917,300 | ) | | | (15,809,125 | ) | | | (24,057,191 | ) | | | (24,162,166 | ) | |
Other income (expense): | | | | | | | | | | | | | | | | | |
Sublease income | | | 27,241 | | | | — | | | | 64,138 | | | | — | | |
Loss on debt conversion with related party | | | — | | | | — | | | | — | | | | (6,134,120 | ) | |
Interest income, net | | | 42,035 | | | | 80,582 | | | | 185,734 | | | | 44,871 | | |
Exchange loss, net | | | (35,757 | ) | | | (17,509 | ) | | | (72,186 | ) | | | (36,251 | ) | |
Total other income (expense), net | | | 33,519 | | | | 63,073 | | | | 177,686 | | | | (6,125,500 | ) | |
Loss before income taxes | | | (4,883,781 | ) | | | (15,746,052 | ) | | | (23,879,505 | ) | | | (30,287,666 | ) | |
Deferred income tax benefit (expense) | | | 839 | | | | 1,436 | | | | 2,480,340 | | | | (189,255 | ) | |
Net Loss | | | (4,882,942 | ) | | | (15,744,616 | ) | | | (21,399,165 | ) | | | (30,476,921 | ) | |
Accrual of paid-in-kind dividends on Series A non-voting convertible preferred stock | | | — | | | | — | | | | — | | | | (1,256,662 | ) | |
Net loss attributable to common stockholders | | $ | (4,882,942 | ) | | $ | (15,744,616 | ) | | $ | (21,399,165 | ) | | $ | (31,733,583 | ) | |
Net loss per share of common stock — basic and diluted | | $ | (0.14 | ) | | $ | (8.20 | ) | | $ | (0.63 | ) | | $ | (18.02 | ) | |
Weighted average shares outstanding — basic and diluted | | | 34,129,553 | | | | 1,919,433 | | | | 33,936,760 | | | | 1,761,237 | | |
| | | | | | | | | | | | | | | | | |
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Condensed Consolidated Balance Sheet Data | September 30, | | | December 31, | | ||
| 2026 | | | 2025 | | ||
| | | | | | | |
Cash and cash equivalents | $ | 4,948,266 | | | $ | 6,524,744 | |
Total assets | | 75,608,219 | | | | 90,171,237 | |
Total liabilities | | 11,475,000 | | | | 15,274,370 | |
Total stockholders’ equity | | 64,133,219 | | | | 74,896,867 | |
Source: Dogwood Therapeutics, Inc.
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