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Dogwood to Host Virtual KOL Event to Discuss Halneuron® for the Treatment of Chemotherapy Induced Neuropathic Pain on September 1, 2026

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Dogwood Therapeutics (Nasdaq: DWTX) will host a virtual key opinion leader event on September 1, 2026 at 10:00 AM ET to discuss Halneuron® for treating chemotherapy induced neuropathic pain (CINP). Expert speakers and management will cover the NaV 1.7 pain-signaling mechanism, Halneuron’s selective non-opioid profile, and prior pre-clinical and clinical data.

According to Dogwood Therapeutics, the event will also review positive interim results from the ongoing randomized Phase 2b CINP trial (HAL-CINP; NCT06848348), where 210–240 U.S. patients receive 8 subcutaneous doses over 14 days, and will discuss synthetic Tetrodotoxin manufacturing to support planned Phase 3 development.

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Positive

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Negative

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Market Context

DWTX's active, effective S-3 is a resale registration for 6,433,126 shares, while this announcement ...
Analysis

DWTX's active, effective S-3 is a resale registration for 6,433,126 shares, while this announcement concerns Halneuron. The filing says Dogwood receives no proceeds; low short positioning provides additional context without establishing a reaction.

Key Figures

KOL Event Date: September 1, 2026 at 10:00 AM Eastern Time Patients Tested: more than 800 patients Trial Phase: Phase 2b +5 more
8 metrics
KOL Event Date September 1, 2026 at 10:00 AM Eastern Time Scheduled virtual event
Patients Tested more than 800 patients Halneuron clinical and pre-clinical development
Trial Phase Phase 2b HAL-CINP CINP study
Planned Sample Size approximately 210 to 240 patients HAL-CINP randomized trial
Doses 8 sub-cutaneous doses Administered over the treatment period
Dosing Period 14 days HAL-CINP treatment period
Follow-up 28 days HAL-CINP safety and effectiveness follow-up
Study Sites approximately 25 sites U.S. clinical trial sites

Historical Context

5 past events · Latest: Aug 13 (Negative)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Aug 13 Q2 earnings report Negative +1.8% Quarterly loss and impairment contrasted with clinical progress and funding-through-readout commentary.
Jul 20 Phase 2b enrollment Positive +0.0% Enrollment milestone and favorable interim separation from placebo produced no reported price change.
Jun 30 Leadership appointment Positive -9.6% OrbiMed venture partner joined the Scientific Advisory Board as chair.
May 18 Phase 2b extension Positive -7.1% Company began an open-label extension after a positive interim trial assessment.
May 14 Q1 earnings report Positive +6.5% Quarterly results included pipeline progress and a financing-supported cash position.

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

Pattern Detected

Recent company news showed mixed reactions, with positive clinical or operating updates frequently followed by negative or limited price reactions.

Key Terms

nav 1.7, tetrodotoxin, cmc, fast track designation, +1 more
5 terms
nav 1.7 medical
"the novel role of the NaV 1.7 sodium ion channel in pain signaling"
NAV 1.7 denotes a net asset value of 1.7 per share or unit, meaning the total value of a fund’s assets minus its liabilities divided by the number of shares, expressed as 1.7 in whatever currency or unit is being used. It matters to investors because NAV is a snapshot of what each share represents financially—like the per‑share “book value” of a pooled investment—used to compare prices, track performance, and value entries or exits.
tetrodotoxin medical
"the first ever synthetic formulation of Tetrodotoxin"
A naturally occurring neurotoxin that blocks sodium channels in nerve cells, preventing nerves from sending signals and causing paralysis or death at very small doses. It matters to investors because it is a public health and regulatory risk in food safety and marine products, a liability factor for companies involved in seafood and testing, and a focus of pharmaceutical research where its potent biological effect is studied for potential medical uses.
cmc technical
"all of the chemistry, manufacturing and controls (“CMC”)"
Chemistry, Manufacturing, and Controls (CMC) describes the technical documentation and processes that show how a drug or medical product is made, tested for consistent quality, and kept stable from batch to batch. Investors care because strong CMC means a product can be manufactured reliably at scale and meet regulatory standards—similar to proving a recipe can be cooked the same way in any kitchen before restaurants expand—affecting approval, production costs, and potential revenue.
fast track designation regulatory
"has been granted fast track designation from the FDA"
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.
lyophilized drug product technical
"the conversion to Halneuron®, the lyophilized drug product"
A lyophilized drug product is a medication that has been freeze-dried to remove water, leaving a stable powder or cake that is reconstituted with a liquid before use. Like dehydrated food that lasts longer and is easier to ship, this form improves shelf life and temperature stability but requires special manufacturing, packaging, and sometimes cold-chain handling—factors that affect production costs, regulatory review, and supply logistics relevant to investors.

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

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ALPHARETTA, Ga., Aug. 17, 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 that it will host a virtual key opinion leader (KOL) event on Tuesday, September 1, 2026 at 10:00 AM Eastern Time, featuring J. Mark Joyce, M.D. (CNS Healthcare), Iain D. Dukes, D.Phil. (OrbiMed Advisors, Chair Dogwood SAB), and Jerry Evarts, Ph.D. (expert CMC Specialist, Dogwood), who will join company management to discuss the unmet need and current treatment landscape for chemotherapy induced neuropathic pain (“CINP”). To register, click here.

The event will review the novel role of the NaV 1.7 sodium ion channel in pain signaling, which is key to the initiation and conduction of the electrical signals that the brain interprets as pain. Management will discuss Halneuron®’s selective and differentiated NaV 1.7 mechanism of action as compared to current and future NaV inhibitors. The speakers will also review prior Halneuron® pre-clinical and clinical research and the design and projected treatment outcomes of the ongoing Phase 2b CINP study design. Halneuron® has been tested on more than 800 patients to date, including patients suffering from cancer-related pain and CINP. Guest experts will discuss ion channel therapies as a newer approach to treating chronic pain, as well as the existing unmet medical need in treating CINP. The company will review positive interim results from its ongoing Phase 2b clinical trial in patients with a mean duration of five years of painful neuropathy due to their prior chemotherapy treatment and discuss the advancement of the first ever synthetic formulation of Tetrodotoxin to support Halneuron®’s' Phase 3 development.

A live question and answer session will follow the formal presentations.

About J. Mark Joyce, M.D.

J. Mark Joyce, M.D. became an investigator for CNS Healthcare of Jacksonville in September 2003. He earned his medical degree from the University of Alabama School of Medicine and completed his psychiatry residency training at Emory University School of Medicine in 1992. Board certified in psychiatry, Dr. Joyce has extensive experience in the public mental health field and owned a private practice in Atlanta, Georgia prior to relocating to Jacksonville.

About Iain D. Dukes, D.Phil.

Iain D. Dukes, D.Phil. is a Venture Partner and joined OrbiMed in 2016. Most recently, Iain was a Senior Vice President, Business Development & Licensing, at Merck where he oversaw all licensing deals for Merck Research Laboratories, including external research, out-licensing, regional deals, and academic alliances. Iain has more than 20 years of experience in pharmaceutical research, drug discovery, scientific and technology licensing, and start-up company leadership, as well as consulting for numerous biotech and venture capital organizations. Before joining Merck, he served as Vice President of External Research and Development at Amgen. He has also held positions as president and CEO of Essentialis Therapeutics and as Vice President, Scientific and Technology Licensing at GlaxoSmithKline. Iain received his D.Phil. degree from the University of Oxford and conducted post-doctoral studies at the University of Pennsylvania on the biophysics of cardiac ion channels.

About Jerry Evarts, Ph.D.

Jerry Evarts, Ph.D. is an expert chemistry and manufacturing consultant working with Dogwood, bringing over 20 years of industrial experience specializing in chemical synthesis of small molecules. Following his doctorate at Purdue University and a post-doctoral at Stanford, Dr. Evarts started his career with Icos Corporation in Bothell, Washington. After two years at the bench, he left to manage all of the chemistry, manufacturing and controls (“CMC”) that was out licensed to a startup, Calistoga Pharma. Dr. Evarts also worked as a bench chemist performing medicinal chemistry, and later pursuing process chemistry and CMC, he moved on to another startup, Acerta Pharma. Following the startup successes, Dr. Evarts turned his attention to consulting with emphasis on startups. Since 2016, he has experienced all levels of programs from early scouting and scale up support for medicinal chemistry, to Phase 3 programs and NDA submissions. Also, starting in 2019, Dr. Evarts managed all drug substance programs for Day One Bio. At Dogwood, he supports the synthetic manufacture of Tetrodotoxin, a molecule requiring over 30 steps of synthetic chemistry, and the conversion to Halneuron®, the lyophilized drug product.

Halneuron® CINP Phase 2b Trial (“HAL-CINP”) Overview (NCT06848348)

HAL-CINP is a randomized, Phase 2b clinical trial evaluating the efficacy and safety of Halneuron® compared with placebo in approximately 210 to 240 patients with moderate to severe neuropathic pain caused by prior platinum and/or taxane-based chemotherapy. Participants receive 8 sub-cutaneous doses of Halneuron® or placebo over a 14-day period and are followed for a total of 28 days for safety and effectiveness. The primary endpoint for this study is the change from baseline to week four in the weekly average of daily 24-hour recall pain intensity scores. The study is being conducted at approximately 25 sites in the U.S. Secondary measures will assess Halneuron’s® treatment effects on sleep, fatigue, neuropathy symptoms and overall patient health.

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 chemotherapy induced peripheral neuropathy 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.

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


FAQ

When is Dogwood Therapeutics' (Nasdaq: DWTX) virtual KOL event on Halneuron for CINP?

The virtual KOL event is scheduled for September 1, 2026 at 10:00 AM Eastern Time. According to Dogwood Therapeutics, expert clinicians and company management will discuss Halneuron®, chemotherapy induced neuropathic pain, and ongoing clinical development, followed by a live question-and-answer session.

What will Dogwood Therapeutics discuss about Halneuron at the September 1, 2026 DWTX KOL event?

The event will focus on Halneuron’s non-opioid NaV 1.7 mechanism and CINP treatment. According to Dogwood Therapeutics, speakers will review pre-clinical and clinical research, positive interim Phase 2b results, and the role of synthetic Tetrodotoxin in supporting future Phase 3 development.

What is the design of Dogwood Therapeutics' Halneuron CINP Phase 2b trial (HAL-CINP, NCT06848348)?

HAL-CINP is a randomized Phase 2b trial in about 210–240 CINP patients comparing Halneuron® to placebo. According to Dogwood Therapeutics, participants receive 8 subcutaneous doses over 14 days, are followed for 28 days, and the primary endpoint is change in weekly average pain intensity at week four.

How many patients have been treated with Halneuron to date, according to Dogwood Therapeutics (DWTX)?

Halneuron® has been tested in more than 800 patients to date. According to Dogwood Therapeutics, this includes individuals with cancer-related pain and chemotherapy induced neuropathic pain, providing a substantial clinical experience base for its non-opioid NaV 1.7 analgesic mechanism.

Does Halneuron for CINP have FDA fast track designation for Dogwood Therapeutics (DWTX)?

Yes, Halneuron® has received FDA fast track designation for treating chemotherapy induced neuropathic pain. According to Dogwood Therapeutics, Halneuron is a selective NaV 1.7 analgesic that has shown pain reduction in clinical studies for general cancer pain and chronic CINP.