STOCK TITAN

Dogwood Therapeutics Announces First Quarter 2026 Financial Results

(Moderate)
(Very Positive)
Tags

Dogwood Therapeutics (Nasdaq:DWTX) reported Q1 2026 results and pipeline progress. The Halneuron® Phase 2b CINP trial has enrolled 164 patients, with top-line data expected in fall 2026. SP16 received FDA IND clearance for a fully NCI-funded Phase 1b CIPPN trial.

The company announced a worldwide development and commercialization partnership for legacy antiviral assets with potential value up to $100M. Q1 2026 R&D expenses were $2.7M and G&A $2.4M. Net loss was $5.0M ($0.15/share). Cash of $13.2M is expected to fund operations into Q4 2026.

Loading...
Loading translation...

Positive

  • Halneuron® Phase 2b trial enrolled 164 patients; top-line data fall 2026
  • SP16 FDA IND clearance; Phase 1b CIPPN trial fully funded by NCI
  • Antiviral partnership with potential value up to $100M to Dogwood and shareholders
  • January 2026 financing of up to $26.9M; $12.5M gross proceeds received
  • Q1 2026 net loss reduced to $5.0M from $12.2M year over year
  • Cash of $13.2M expected to provide runway into Q4 2026

Negative

  • Company reports Q1 2026 net loss of $5.0M, or $0.15 per share
  • R&D expenses rose to $2.7M from $2.4M year over year
  • G&A expenses increased to $2.4M from $2.0M year over year

News Market Reaction – DWTX

+6.45%
6 alerts
+6.45% Session close to close
+7.3% Peak Tracked
-2.8% Trough Tracked
$66.14M Market Cap
0.4x Rel. Volume

In the May 14 session, DWTX gained 6.45%, reflecting a notable positive market reaction. Argus tracked a peak move of +7.3% during that session. Argus tracked a trough of -2.8% from its starting point during tracking. Our momentum scanner triggered 6 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The stock moved +6.5% in the session following this news. A strong positive reaction aligns with a q...
Analysis

The stock moved +6.5% in the session following this news. A strong positive reaction aligns with a quarter that combined clinical progress, improved net loss of $5.0M and a partnership with potential value up to $100M. Historically, DWTX’s earnings days averaged about -5.59%, so a +9.41% move represented a break from prior selling pressure. However, an effective resale shelf for 6,433,126 shares and prior going‑concern language remained key overhangs to monitor.

Key Figures

Antiviral partnership: up to $100M Halneuron® enrollment: 164 patients Financing size: $26.9M +5 more
8 metrics
Antiviral partnership up to $100M Potential value to Dogwood and current/former shareholders
Halneuron® enrollment 164 patients Phase 2b CINP study enrolled as of Q1 2026
Financing size $26.9M Financing completed in January 2026 to progress Halneuron®
Financing proceeds $12.5M Gross proceeds received from January 2026 financing
Cash balance $13.2M Cash on hand at March 31, 2026; runway into Q4 2026
R&D expenses $2.7M vs $2.4M Q1 2026 vs Q1 2025 research and development spend
Net loss $5.0M vs $12.2M Q1 2026 net loss vs Q1 2025
Net loss per share $0.15 vs $8.45 Q1 2026 basic/diluted loss per share vs Q1 2025

Previous Earnings Reports

5 past events · Latest: Mar 18 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Mar 18 Earnings & pipeline Positive -7.8% Q4 and 2025 results with Halneuron® progress and new financing details.
Nov 06 Quarterly earnings Positive -6.5% Q3 2025 results, Halneuron® enrollment updates and SP16 license closing.
Aug 13 Quarterly earnings Positive -1.0% Q2 2025 results highlighting Halneuron® enrollment and CINP trial progress.
May 08 Quarterly earnings Positive -1.5% Q1 2025 results, initial Halneuron® Phase 2b dosing and cash runway detail.
Mar 31 Annual results Positive -11.2% Q4 and 2024 results with debt-to-equity conversion and cash runway extension.

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 typically been followed by negative price reactions, despite operational and pipeline progress.

Recent Company History

Over the past several quarters, Dogwood’s earnings updates have consistently paired pipeline advances with share-price weakness. Prior reports from Mar 18, 2026, Nov 6, 2025, Aug 13, 2025, May 8, 2025, and Mar 31, 2025 all saw negative next‑day moves despite milestones such as growing Halneuron® Phase 2b enrollment, SP16 licensing, and extended cash runway. Today’s first‑quarter 2026 results continue the narrative of clinical and financial progress but coincide with a positive pre‑news setup, contrasting with the historical pattern of post‑earnings weakness.

Key Terms

phase 2b, investigational new drug application, nav 1.7 inhibitor, fast track designation, +3 more
7 terms
phase 2b medical
"Halneuron® Phase 2b trial in Chemotherapy Induced Neuropathy on track"
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.
investigational new drug application regulatory
"FDA acceptance of SP16 Investigational New Drug Application for the treatment"
An investigational new drug application is a formal request made to regulatory authorities to begin testing a new medication in humans. It is a critical step in the drug development process, as approval indicates the drug has passed initial safety checks and can be studied further. For investors, this signals that a potential new treatment is progressing through its early testing stages, which can impact the company's future growth prospects.
nav 1.7 inhibitor medical
"Halneuron® is in Phase 2b clinical development as a non-opioid, NaV 1.7 inhibitor"
A Nav 1.7 inhibitor is a drug that blocks the Nav1.7 protein, a specific pathway nerve cells use to send pain signals to the brain. Investors care because drugs targeting this channel aim to relieve pain without the addiction risks of opioids, so successful candidates can create large markets or change prescribing patterns; however, clinical and regulatory success is uncertain, making such programs high-risk, high-reward for biotech investors.
fast track designation regulatory
"Halneuron® has been granted fast track designation from the Food and Drug Administration"
Fast track designation is a status the U.S. Food and Drug Administration grants to drugs intended to treat serious conditions and address an unmet medical need. It gives the developer more frequent communication with the FDA and can allow parts of the application to be reviewed on a rolling basis, and it may pave the way to priority review or accelerated approval. It can shorten development timelines, though it does not guarantee approval.
alpha-1-antitrypsin medical
"provides alpha-1-antitrypsin-like activity. Consistent with alpha-1-antitrypsin"
Alpha-1-antitrypsin is a protective protein made by the liver that acts like a brake or shield in the lungs, preventing other proteins from damaging lung tissue; inherited deficiency can lead to serious lung and liver disease. Investors care because tests, replacement therapies, gene treatments and diagnostics aimed at correcting or detecting this deficiency can drive regulatory approvals, pricing decisions and revenue opportunities in the rare-disease and respiratory markets.
tnf-alpha medical
"potential reductions in IL-6, IL-8, IL1B and TNF-alpha levels"
Tumor necrosis factor-alpha (TNF-alpha) is a small signaling protein the body uses to trigger and regulate inflammation, like a fire alarm that summons immune cells to a problem site. Investors watch it because elevated or controlled TNF-alpha levels are central to many inflammatory and autoimmune diseases, making it a common target for drugs and diagnostics; success or failure of therapies that block or measure TNF-alpha can greatly affect company value and market prospects.

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

See more from StockTitan in Google Search and AI answers. Adds StockTitan as a preferred source · opens Google
Add on Google

Halneuron® Phase 2b trial in Chemotherapy Induced Neuropathy on track for top-line results in fall 2026 -

- FDA acceptance of SP16 Investigational New Drug Application for the treatment of Chemotherapy Induced Pain and Neuropathy –

- Announces Worldwide Development and Commercialization Partnership for Legacy Antiviral Assets with potential value up to $100M to Dogwood and its current and former shareholders -

ALPHARETTA, Ga., May 14, 2026 (GLOBE NEWSWIRE) -- 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 first quarter ended March 31, 2026.

“Dogwood is off to a strong operational start to 2026 driven by significant pipeline progress for both Halneuron®, with Phase 2b data anticipated this fall, and SP16, which received FDA clearance to progress into Phase 1b development this quarter,” said Greg Duncan, Chief Executive Officer of Dogwood Therapeutics. “Furthermore, we executed a global development license for our legacy combination antiviral assets.”

Key Highlights

  • The Company currently has enrolled 164 patients in its Halneuron® Phase 2b Chemotherapy Induced Neuropathic Pain (“CINP”) study, with top-line results expected fall of 2026.
  • SP16 granted IND approval from the FDA. Study to begin enrolling in mid-2026 for the treatment of chemotherapy-induced pain and peripheral neuropathy (“CIPPN”). It is fully funded by the National Cancer Institute and will be conducted at the University of Virginia.
  • 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.
  • Cash on hand of $13.2 million provides operational runway into the fourth quarter of 2026.

Dogwood Therapeutics Proprietary Pipeline Includes:

  • Halneuron® is in Phase 2b clinical development as a non-opioid, NaV 1.7 inhibitor 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. Top line results from the ongoing Phase 2b trial are expected in the fall of 2026.
  • 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 Phase 1b CIPPN trial is fully funded by the National Cancer Institute.

First Quarter 2026 Financial Results

Research and development expenses for the first quarter of 2026 were $2.7 million, compared to $2.4 million for the first quarter of 2025. The $0.3 million increase quarter over quarter was primarily related to an increase in drug development costs for Halneuron® of $0.1 million and salaries and related personnel costs of $0.2 million.

General and administrative expenses for the first quarter of 2026 were $2.4 million, compared to $2.0 million for the first quarter of 2025. The $0.4 million increase quarter over quarter was primarily due to an increase in salaries and related personnel costs of $0.5 million offset by a decrease in franchise fees of $0.1 million.

Net loss attributable to common stockholders for the first quarter of 2026 was $5.0 million or $0.15 basic and diluted net loss per share, compared to a net loss attributable to common stockholders of $12.2 million, or $8.45 basic and diluted net loss per share, for the first 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. 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 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 CIPPN 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).

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. 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-

DOGWOOD THERAPEUTICS, INC.
Selected Financial Data
(unaudited)

   
Condensed Consolidated
Statements of Operations Data
Three Months Ended
March 31,
 
   2026   2025 
Revenue $  $ 
Operating expenses:        
Research and development  2,669,779   2,436,998 
General and administrative  2,406,587   1,992,928 
Total operating expenses  5,076,366   4,429,926 
Loss from operations  (5,076,366)  (4,429,926)
Other income (expense):        
Sublease income  19,455    
Loss on debt conversion with related party     (6,134,120)
Interest income (expense), net  77,350   (147,090)
Exchange loss, net  (5,860)  (23,274)
Total other income (expense), net  90,945   (6,304,484)
Loss before income taxes  (4,985,421)  (10,734,410)
Deferred income tax expense  (1,193)  (190,542)
Net Loss  (4,986,614)  (10,924,952)
Accrual of paid-in-kind dividends on Series A non-voting convertible preferred stock     (1,256,662)
Net loss attributable to common stockholders $(4,986,614) $(12,181,614)
Net loss per share of common stock — basic and diluted $(0.15) $(8.45)
Weighted average shares outstanding — basic and diluted  33,544,748   1,441,535 
         


Condensed Consolidated Balance Sheet DataMarch 31,  December 31, 
 2026  2025 
        
Cash and cash equivalents$13,227,839  $6,524,744 
Total assets 95,207,871   90,171,237 
Total liabilities 14,584,519   15,274,370 
Total stockholders’ equity 80,623,352   74,896,867 
        

Source: Dogwood Therapeutics, Inc.


FAQ

What were Dogwood Therapeutics (DWTX) first quarter 2026 financial results?

Dogwood Therapeutics reported a Q1 2026 net loss of $5.0 million, or $0.15 per share. According to Dogwood Therapeutics, R&D expenses were $2.7 million and G&A expenses were $2.4 million, with $13.2 million in cash on hand.

How is Dogwood Therapeutics (DWTX) progressing its Halneuron Phase 2b trial in 2026?

Dogwood Therapeutics has enrolled 164 patients in its Halneuron Phase 2b CINP study. According to Dogwood Therapeutics, top-line results from this non-opioid NaV 1.7 inhibitor trial are expected in the fall of 2026, supporting development in chemotherapy-induced neuropathic pain.

What is the status of Dogwood Therapeutics’ SP16 program for chemotherapy-induced pain?

SP16 received FDA acceptance of its IND for chemotherapy-induced pain and neuropathy. According to Dogwood Therapeutics, a fully National Cancer Institute-funded Phase 1b CIPPN trial at the University of Virginia is expected to begin enrolling patients in mid-2026.

What does the antiviral partnership mean for Dogwood Therapeutics (DWTX) and shareholders?

Dogwood Therapeutics announced a worldwide development and commercialization partnership for its legacy antiviral assets. According to Dogwood Therapeutics, the agreement has potential value of up to $100 million to the company and its current and former shareholders, adding non-dilutive upside.

How long can Dogwood Therapeutics’ cash runway support operations after Q1 2026?

Dogwood Therapeutics reported $13.2 million in cash on hand as of Q1 2026. According to Dogwood Therapeutics, this balance, alongside prior financing, is expected to fund operations into the fourth quarter of 2026, assuming current plans and spending levels.

How did Dogwood Therapeutics’ expenses change year over year in Q1 2026?

Dogwood Therapeutics’ Q1 2026 R&D expenses rose to $2.7 million and G&A to $2.4 million. According to Dogwood Therapeutics, R&D increased $0.3 million and G&A $0.4 million versus Q1 2025, mainly from higher salaries and development costs.