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Neuphoria Responds to the announcement made by London-listed Scancell Holdings plc

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Neuphoria Therapeutics (NASDAQ: NEUP) confirmed it is in discussions with London-listed Scancell Holdings about a potential acquisition of Neuphoria by Scancell. Any deal could result in Scancell becoming a Nasdaq-listed company. There is currently no certainty on reaching agreement, final terms, or completion.

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Positive

  • Formal confirmation of acquisition talks between Neuphoria and Scancell
  • Potential transaction could lead to Scancell becoming Nasdaq-listed

Negative

  • Company states there is no certainty any agreement or transaction will be reached
  • No financial terms, structure, or timing of the potential deal disclosed

News Market Reaction – NEUP

-3.72%
5 alerts
-3.72% Session close to close
+3.8% Peak Tracked
-13.8% Trough Tracked
$24.70M Market Cap
0.1x Rel. Volume

In the Jun 29 session, NEUP declined 3.72%, reflecting a moderate negative market reaction. Argus tracked a peak move of +3.8% during that session. Argus tracked a trough of -13.8% from its starting point during tracking. Our momentum scanner triggered 5 alerts that day, indicating moderate trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement highlights active combination talks following Neuphoria’s strategic shift, with ca...
Analysis

This announcement highlights active combination talks following Neuphoria’s strategic shift, with cash of $19.4M and prior restructuring weighing on context. Key risks are deal uncertainty and terms; investors will watch for a definitive agreement or termination update.

Key Figures

Share price: $4.35 Daily price move: -3.12% Market cap: $24,266,434 +5 more
8 metrics
Share price $4.35 Prior to combination talks announcement
Daily price move -3.12% 24h change before news
Market cap $24,266,434 Equity value prior to announcement
Quarterly net loss $0.5M Three months ended March 31, 2026
Equity raised $17.9M Net proceeds from equity sales reported in 10-Q
Cash & equivalents $19.4M Balance at March 31, 2026
Working capital $20.1M As of March 31, 2026
Restructuring costs $1.3M Recorded over nine months tied to strategic shift

Key Terms

phase 3, restricted stock units, schedule 13g
3 terms
phase 3 medical
"AFFIRM‑1 phase 3 trial in social anxiety disorder"
Phase 3 is the late-stage clinical testing step for a new drug or medical treatment, where the product is given to large groups of patients to confirm effectiveness, monitor side effects, and compare it to standard care. Successful Phase 3 results are often the final scientific hurdle before regulators decide on approval and market launch—like passing a final exam before graduation—and can sharply change a company's valuation and future revenue prospects.
restricted stock units financial
"reported receiving 8,537 restricted stock units (RSUs) of the company"
Restricted stock units are a type of company reward where employees are promised shares of stock, but they only fully own these shares after meeting certain conditions, like staying with the company for a set time. They matter because they can become valuable assets and are often used to motivate employees to help the company succeed.
schedule 13g regulatory
"filed an amended Schedule 13G reporting a passive ownership stake"
A Schedule 13G is a formal document that investors file with the government when they acquire a large ownership stake in a company, usually for investment purposes rather than control. It helps keep the public informed about who owns significant parts of a company's shares, which can influence how the company is managed and how investors make decisions. Filing this schedule is important for transparency and understanding the ownership landscape of publicly traded companies.

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

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Neuphoria Therapeutics confirms it is in talks with Scancell Holdings plc about a possible combination

BURLINGTON, Mass., June 26, 2026 (GLOBE NEWSWIRE) -- Neuphoria Therapeutics Inc. (“Neuphoria” or the “Company”) (NASDAQ: NEUP), a clinical-stage biotechnology company dedicated to developing therapies that address the complex needs of individuals affected by neuropsychiatric disorders, today issued the following statement in response to an announcement made by London-listed biotechnology company Scancell Holdings plc (“Scancell”).

The Neuphoria Board notes the announcement made by Scancell earlier today about a possible combination with Neuphoria. The Scancell announcement was made following speculation in the UK press and in compliance with UK regulations.

The Board can confirm that it is in discussions with Scancell about the potential acquisition of Neuphoria by Scancell, with Scancell becoming a Nasdaq-listed company following closing of any such transaction.

There can be no certainty that any agreement will be reached with Scancell, the terms of any transaction or if any transaction will proceed at all.

Any further announcements will be made in compliance with applicable SEC and Nasdaq regulations.

About Neuphoria Therapeutics Inc.

Neuphoria Therapeutics Inc. (Nasdaq: NEUP) is a public company incorporated in Delaware. The Company is a clinical-stage biotechnology company dedicated to developing therapies that address the complex needs of individuals affected by neuropsychiatric disorders. Neuphoria is advancing the lead drug candidate, BNC210, an oral, proprietary, selective negative allosteric modulator of the α7 nicotinic acetylcholine receptor for the treatment of post-traumatic stress disorder (“PTSD”). BNC210 is a first-of-its-kind, well tolerated, broad spectrum anti-anxiety experimental therapeutic, designed to restore neurotransmitter balance in relevant brain areas, providing rapid relief from stress and anxiety symptoms without the common pitfalls of sedation, cognitive impairment, or addiction. Following the announcement from the AFFIRM-1 Phase 3 clinical trial on October 20, 2025, in which the Company announced that the trial missed its primary and secondary endpoints, the Company has halted development of BNC210 in social anxiety disorder and is conducting a strategic review. In addition, Neuphoria has a strategic partnership with two drugs in early-stage clinical trials for the treatment of cognitive deficits in Alzheimer’s disease and other central nervous system conditions. Neuphoria’s pipeline also includes the α7 nicotinic acetylcholine receptor next generation and the Kv3.1/3.2 preclinical programs, both in the lead optimization development stage.

Forward-Looking Statements

Neuphoria cautions that statements included in this press release that are not a description of historical facts are forward-looking statements. Words such as “may,” “could,” “will,” “would,” “should,” “expect,” “plan,” “anticipate,” “believe,” “estimate,” “intend,” “predict,” “seek,” “contemplate,” “potential,” “continue” or “project” or the negative of these terms or other comparable terminology are intended to identify forward-looking statements. The forward-looking statements are based on our current beliefs, plans, burn rate and expectations. Certain forward-looking statements, including (without limitation) about (1) Neuphoria’s ability to develop and expand its business, successfully complete development of its current product candidates, the timing of commencement and/or completion, as well as any successful or other outcome of various clinical trials, and receipt of data and current and future collaborations for the development and commercialization of its product candidates, (2) the market for drugs to treat central nervous system diseases and pain conditions, and the Company’s ability to realize the commercial potential of its products, as well as its regulatory strategy related to its clinical trials and, if successful, the regulatory pathway to any next stage in development or commercialization, (3) Neuphoria’s financial resources, and capital allocation and corporate development strategy, (4) the Board’s review of strategic alternatives and evaluation of offers from third parties, and (5) assumptions underlying any such statements. The inclusion of forward-looking statements should not be regarded as a representation by Neuphoria that any of its plans will be achieved. Future events and actual results could differ materially from those set out in, contemplated by or underlying the forward-looking statements due to a number of important factors. Certain forward-looking statements involve contracts, licenses and arrangements involving third parties and their respective clinical trial and research and development projects that are out of our control, including our agreements with our strategic partners. They may terminate or delay any or all such projects in their discretion pursuant to the terms of our agreements with them, which could result in the Company not realizing any further milestone payments or further progress on the respective product pathways. Actual results may differ materially from those set forth in this release due to the risks and uncertainties inherent in the Company’s business and other risks described in the Company’s filings with the SEC, including the Company’s Annual Report on Form 10-K, Quarterly Report on Form 10-Q, Current Reports on Form 8-K, each filed with the SEC, and its other reports. Investors are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date hereof, and Neuphoria undertakes no obligation to revise or update this news release to reflect events or circumstances after the date hereof. Further information regarding these and other risks, uncertainties and other factors is included in Neuphoria’s filings with the SEC, copies of which are available from the SEC’s website (www.sec.gov) and on Neuphoria’s website (www.neuphoriatx.com) under the heading “Investor Center.” All forward-looking statements are qualified in their entirety by this cautionary statement. This caution is made under the safe harbor provisions of Section 21E of the Private Securities Litigation Reform Act of 1995. Neuphoria expressly disclaims all liability in respect to actions taken or not taken based on any or all the contents of this press release. 

FOR FURTHER INFORMATION PLEASE CONTACT:

General

Spyridon (Spyros) Papapetropoulos
spyros@neuphoriatx.com 

IR & PR

Argot Partners
neuphoria@argotpartners.com


FAQ

What acquisition talks did Neuphoria Therapeutics (NASDAQ: NEUP) confirm with Scancell on June 26, 2026?

Neuphoria confirmed it is in discussions with Scancell about a potential acquisition of Neuphoria by Scancell. According to Neuphoria, the talks follow Scancell’s earlier announcement and UK press speculation, but no binding agreement or transaction terms have been reached.

Could the potential Scancell acquisition of Neuphoria (NEUP) lead to a Nasdaq listing for Scancell?

Neuphoria stated that any completed acquisition could result in Scancell becoming a Nasdaq-listed company. According to Neuphoria, this outcome would follow closing of a potential transaction, which remains uncertain and subject to reaching a definitive agreement and regulatory compliance.

How certain is it that Scancell will acquire Neuphoria Therapeutics (NEUP)?

Neuphoria emphasized there can be no certainty that any agreement or transaction with Scancell will occur. According to Neuphoria, details such as final terms, structure, and timing remain undecided, and discussions may end without a completed acquisition or listing change.

Why did Neuphoria issue a statement about Scancell on June 26, 2026?

Neuphoria issued the statement in response to Scancell’s earlier announcement about a possible combination and related UK press speculation. According to Neuphoria, the communication also aligns with UK, SEC, and Nasdaq regulatory requirements for disclosure during ongoing transaction discussions.

What regulatory steps will Neuphoria (NEUP) follow regarding any potential Scancell transaction?

Neuphoria said that any further announcements about a potential Scancell acquisition will follow applicable SEC and Nasdaq regulations. According to Neuphoria, Scancell’s initial announcement was made to comply with UK regulations, and both parties must adhere to their respective market disclosure rules.