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Dogwood Therapeutics Reports Fourth Quarter and Full Year 2025 Financial Results

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Dogwood Therapeutics (Nasdaq: DWTX) reported Q4 and full-year 2025 results and clinical updates. Key items: interim Phase 2b analysis showed Halneuron® separating from placebo in a 97-patient subset; 143 patients recruited; trial >50% enrolled with top-line data expected in Q3 2026. The company completed a financing of up to $26.9M, receiving $12.5M gross and $11.4M net in Jan 2026, and had $6.5M cash at Dec 31, 2025, expected to fund operations into Q4 2026.

Full-year R&D rose to $21.8M vs $3.5M in 2024; net loss was $35.5M or $7.13 per share.

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Positive

  • Interim Phase 2b signal in 97-patient subset
  • 143 patients recruited to Halneuron® trial
  • Financing up to $26.9M secured to fund Phase 2b
  • Company expects funding into Q4 2026

Negative

  • Full-year net loss $35.5M (2025)
  • Cash and cash equivalents of only $6.5M at Dec 31, 2025
  • R&D spend increased to $21.8M from $3.5M in 2024

News Market Reaction – DWTX

-7.76% 2.0x vol
5 alerts
-7.76% Session close to close
-12.5% Trough in 28 hr 56 min
$101.22M Market Cap
2.0x Rel. Volume

In the Mar 18 session, DWTX declined 7.76%, reflecting a notable negative market reaction. Argus tracked a trough of -12.5% from its starting point during tracking. Our momentum scanner triggered 5 alerts that day, indicating moderate trading interest and price volatility. Trading volume was elevated at 2.0x the daily average, suggesting increased selling activity.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock moved -7.8% in the session following this news. A negative reaction despite operational pr...
Analysis

The stock moved -7.8% in the session following this news. A negative reaction despite operational progress would fit a pattern where earnings-day updates focus attention on losses and dilution risk. FY 2025 net loss reached $35.5M and Q4 operating spend stayed meaningful, while an S‑3 registers 6,433,126 shares for resale. Historically, earnings news has averaged a -4.04% move, so further downside could be viewed within that established response range.

Key Figures

Halneuron Phase 2b enrollment: 143 patients Interim analysis cohort: 97 patients Planned sample size: 210–240 patients +5 more
8 metrics
Halneuron Phase 2b enrollment 143 patients Ongoing Halneuron® Phase 2b CINP trial recruitment
Interim analysis cohort 97 patients Subset in Halneuron® Phase 2b interim analysis
Planned sample size 210–240 patients Expected to provide 80–85% power vs placebo
Financing size up to $26.9M January 2026 financing to progress Halneuron® Phase 2b
Financing gross proceeds $12.5M Gross proceeds already received from January 2026 financing
Q4 2025 net loss $3.8M ($0.26/share) Net loss attributable to common stockholders, Q4 2025
FY 2025 net loss $35.5M ($7.13/share) Net loss attributable to common stockholders, year ended 2025
Cash and equivalents $6.5M Cash and cash equivalents as of December 31, 2025

Previous Earnings Reports

5 past events · Latest: Nov 06 (Neutral)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Nov 06 Q3 2025 earnings Neutral -6.5% Reported higher R&D from SP16 acquisition and increased net loss with limited cash runway.
Aug 13 Q2 2025 earnings Neutral -1.0% Updated Halneuron Phase 2b progress and cash runway with modest operating losses.
May 08 Q1 2025 earnings Neutral -1.5% Outlined early Phase 2b dosing, higher R&D and G&A, and Nasdaq compliance status.
Mar 31 FY 2024 earnings Neutral -11.2% Reported larger 2024 net loss, higher expenses, and strengthened cash via equity raises.
Nov 07 Q3 2024 earnings Neutral +0.0% Post-combination update on pipeline, new financing, and increased quarterly net loss.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Earnings releases have historically seen a modestly negative average move of -4.04%, suggesting past financial updates often weighed on sentiment.

Recent Company History

Across the last five earnings releases from Nov 2024 through Nov 2025, Dogwood coupled financial updates with progress on Halneuron® and capital structure moves, including debt-to-equity conversion and licensing SP16. These events typically produced small to moderate share price declines, averaging -4.04%. Compared with those periods, the current report adds higher 2025 R&D, a larger net loss, but also a streamlined Q4 G&A and a clearer cash runway tied to recent financings.

Key Terms

phase 2b, interim analysis, independent statistical review committee, placebo, +1 more
5 terms
phase 2b medical
"recruitment of 143 patients in our ongoing Halneuron® Phase 2b trial"
Phase 2b is a stage in the development of a new medicine or treatment where researchers test its effectiveness and safety in a larger group of people. This step helps determine whether the treatment works well enough to move forward and if it has manageable side effects, which is important for investors because successful results can lead to potential approval and market opportunity.
interim analysis medical
"In December 2025, the Company announced the results of an interim analysis of the Halneuron® Phase 2b trial."
An interim analysis is an early review of a project or process before it is fully completed. For investors, it provides a snapshot of progress or performance, helping to identify whether things are on track, need adjustment, or should be stopped early. Think of it as a progress report that can influence decisions before the final outcome is known.
independent statistical review committee medical
"The independent statistical review committee concluded that Halneuron® was separating from placebo"
A committee of outside experts who independently check how clinical or study data are analyzed and interpreted, acting like a neutral referee for the numbers. They verify that the analysis methods are appropriate, rerun or review results, and flag errors or bias so regulators, investors and management can trust the reported findings. Investors care because an independent review lowers the risk of misleading results and can affect regulatory approval, market value and confidence in a company’s claims.
placebo medical
"concluded that Halneuron® was separating from placebo in the 97 patient subset"
A placebo is an inactive pill, injection or procedure that looks and feels like the real treatment but contains no therapeutic ingredient, often called a sugar pill. Investors care because comparing a drug to a placebo reveals whether observed benefits come from the medicine itself or from expectation; clear superiority over placebo reduces regulatory and commercial risk, much like a blind taste test proves a new recipe really tastes better.
statistically significant medical
"expected to provide 80-85% power to see a statistically significant Halneuron® pain reduction result"
"Statistically significant" means that a result or difference observed in data is unlikely to have occurred by chance alone, suggesting there is a real underlying effect. For investors, it indicates that the findings or patterns they see are likely meaningful and not just random noise, helping them make more informed decisions based on reliable information. Think of it as a pattern that is strong enough to stand out clearly from background randomness.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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ATLANTA, March 18, 2026 (GLOBE NEWSWIRE) -- Dogwood Therapeutics, Inc. (Nasdaq: DWTX) (the “Company”), a development-stage biotechnology company developing new medicines to treat pain and neuropathy, today announced financial results for the fourth quarter and full year ended December 31, 2025.

“The Company continues to execute at a high level, including recruitment of 143 patients in our ongoing Halneuron® Phase 2b trial, commencement of a Phase 2b extension trial and the recent execution of a financing to provide us with operational runway through the Phase 2b final data readout later this year,” said Greg Duncan, Chief Executive Officer of Dogwood Therapeutics.

Key Highlights

  • In December 2025, the Company announced the results of an interim analysis of the Halneuron® Phase 2b trial. The independent statistical review committee concluded that Halneuron® was separating from placebo in the 97 patient subset included in the analysis.
  • The independent statistical review committee determined that a sample size of 210-240 is expected to provide 80-85% power to see a statistically significant Halneuron® pain reduction result versus placebo.
  • CINP Phase 2b study is over 50% enrolled, Company expects top-line results in Q3 2026.
  • In January 2026, the Company completed a financing of up to $26.9 million to progress Halneuron® through Phase 2b development, of which gross proceeds of $12.5 million have been received.

Fourth Quarter 2025 Financial Results

Research and development expenses for the fourth quarter of 2025 remained level with the fourth quarter of 2024 at $2.3 million.

General and administrative expenses for the fourth quarter of 2025 were $1.5 million, compared to $5.2 million for the fourth quarter of 2024. The $3.7 million decrease quarter over quarter was primarily due to a decrease in nonrecurring transaction costs of $3.9 million related to the combination with Pharmagesic (Holdings) Inc. in October 2024 and a decrease in salaries and related personnel costs of $0.2 million offset by an increase in legal and professional fees of $0.3 million and expenses associated with being a public company of $0.1 million.

Net loss attributable to common stockholders for the fourth quarter of 2025 was $3.8 million, or $0.26 basic and diluted net loss per share, compared to a net loss attributable to common stockholders of $8.2 million, or $6.29 basic and diluted net loss per share, for the fourth quarter of 2024.

Full Year 2025 Financial Results

Research and development expenses for the year ended December 31, 2025 were $21.8 million, compared to $3.5 million for the year ended December 31, 2024. The $18.3 million increase year over year was primarily related to acquired in-process research and development expenses of $12.0 million associated with the licensing agreement of SP16 and the impact of the business combination with Pharmagesic (Holdings) Inc., including increases in expenses for clinical trials of $6.1 million related to the Halneuron® CINP Phase 2b study, drug development and manufacturing costs of $0.3 million and salaries and related personnel costs of $0.3 million, offset by a decrease in research and preclinical costs of $0.4 million.

General and administrative expenses for the year ended December 31, 2025 were $6.1 million, compared to $8.7 million for the year ended December 31, 2024. The $2.6 million decrease year over year was primarily due to a decrease in nonrecurring transaction costs of $3.9 million related to the combination of Pharmagesic in October 2024 and a decrease in expenses associated with being a public company of $0.2 million offset by increases in salaries and related personnel costs of $0.5 million, legal and professional fees of $0.6 million, franchise tax fees of $0.2 million and other general and administrative costs of $0.2 million.

Net loss attributable to common stockholders for the year ended December 31, 2025 was $35.5 million, or $7.13 basic and diluted net loss per share, compared to a net loss attributable to common stockholders of $12.9 million, or $12.52 basic and diluted net loss per share, for the year ended December 31, 2024.

As of December 31, 2025, Dogwood Therapeutics’ cash and cash equivalents totaled $6.5 million. The Company believes that the cash and cash equivalents on hand at December 31, 2025 together with the net proceeds received in January 2026 of $11.4 million after deducting placement agent fees and offering expenses payable by the Company, is expected to fund operations through the Halneuron® Phase 2b final data readout and into the fourth quarter of 2026.

About Dogwood Therapeutics

Dogwood Therapeutics (Nasdaq: DWTX) is a development-stage biopharmaceutical company focused on developing new medicines to treat pain and neuropathic disorders. The Dogwood 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 Food and Drug Administration (“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 chemotherapy-induced neuropathic pain (“CINP”).

SP16 IV is a low-density lipoprotein receptor related protein-1 (LRP1) agonist 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 CINP trial will commence following consultation with FDA and is fully funded by the National Cancer Institute.

Dogwood Therapeutic’s 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).

For more information, please visit www.dwtx.com.

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. 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:

IR@dwtx.com

-Financial Tables Follow-

DOGWOOD THERAPEUTICS
Selected Financial Data         
(unaudited)

Condensed Statements of
Operations Data
 Three Months Ended
December 31,
  Year Ended
December 31,
 
  2025  2024  2025  2024 
Revenue $  $  $  $ 
Operating expenses:                
Research and development  2,337,788   2,315,950   21,866,071   3,530,913 
General and administrative  1,468,491   5,226,202   6,102,374   8,696,335 
Total operating expenses  3,806,279   7,542,152   27,968,445   12,227,248 
Loss from operations  (3,806,279)  (7,542,152)  (27,968,445)  (12,227,248)
Other income (expense):                
Loss on debt conversion with related party        (6,134,120)   
Loss on fixed asset disposal  (2,731)     (2,731)   
Interest income (expense), net  52,067   (155,436)  96,938   (92,192)
Exchange gain (loss), net  8,335   (30,787)  (27,916)  (30,787)
Total other income (expense)  57,671   (186,223)  (6,067,829)  (122,979)
Loss before income taxes  (3,748,608)  (7,728,375)  (34,036,274)  (12,350,227)
Deferred income tax (expense) benefit  (31,841)  503   (221,096)  503 
Net Loss  (3,780,449)  (7,727,872)  (34,257,370)  (12,349,724)
Accrual of paid-in-kind dividends on Series A Non-Voting Convertible Preferred Stock     (514,105)  (1,256,662)  (514,105)
Net loss attributable to common stockholders $(3,780,449) $(8,241,977) $(35,514,032) $(12,863,829)
Net loss per common share — basic and diluted $(0.26) $(6.29) $(7.13) $(12.52)
Weighted average number of shares outstanding — basic and diluted  14,521,199   1,310,474   4,977,446   1,027,788 
                 

   

Condensed Consolidated Balance Sheet DataDecember 31,  December 31, 
 2025  2024 
        
Cash and cash equivalents$6,524,744  $14,847,949 
Total assets 90,171,237   94,308,246 
Total liabilities 15,274,370   30,027,223 
Total stockholders’ equity (deficit) 74,896,867   (10,124,339)

Source: Dogwood Therapeutics, Inc.


FAQ

What did Dogwood Therapeutics (DWTX) report about the Halneuron® Phase 2b interim analysis on March 18, 2026?

The interim analysis showed Halneuron® separating from placebo in a 97-patient subset. According to the company, an independent statistical review committee observed separation and estimates a 210–240 sample size will provide 80–85% power for a significant pain reduction result.

How many patients has DWTX enrolled in the Halneuron® CINP Phase 2b trial as of March 18, 2026?

Dogwood Therapeutics has recruited 143 patients to date. According to the company, the study is over 50% enrolled and remains on track for top-line results expected in Q3 2026.

What financing did Dogwood Therapeutics announce and how much net proceeds were received in January 2026?

The company completed a financing of up to $26.9 million and received $12.5 million gross. According to the company, net proceeds of $11.4 million were received in January 2026 after fees and expenses.

How long does Dogwood Therapeutics expect its cash to fund operations after the January 2026 proceeds?

Dogwood expects funding through the Phase 2b final data readout and into Q4 2026. According to the company, Dec 31, 2025 cash plus January 2026 net proceeds provide the stated operational runway.

What were Dogwood Therapeutics’ full-year 2025 R&D expenses and net loss per share (basic and diluted)?

R&D expense for 2025 was $21.8 million and net loss per share was $7.13 basic and diluted. According to the company, the R&D increase largely reflects acquired IPRD and clinical trial costs tied to Halneuron® development.

When does Dogwood Therapeutics expect top-line results for the Halneuron® Phase 2b CINP study (DWTX)?

Top-line results are expected in Q3 2026. According to the company, the study is over 50% enrolled and the projected sample size aims to deliver 80–85% statistical power for pain reduction versus placebo.