Neuphoria Responds to Lynx1’s Revised Indication of Interest at a Reduced Price and Premium
Rhea-AI Summary
Neuphoria (NASDAQ: NEUP) said it will continue a robust strategic alternatives review and urged stockholders to vote for its nominees on the WHITE proxy card on Dec 4, 2025. The company paused R&D spending for BNC210 in PTSD while evaluating options and says it has received multiple indications of interest, including nearly a dozen advanced to NDAs and separate process letters. Neuphoria characterized Lynx1’s revised unsolicited bid of $4.75 per share as reduced, near cash value, and not reflecting licensing agreements that generated tens of millions in revenue. The Board said it will review Lynx1’s proposal alongside other offers and warned electing dissident nominees could jeopardize an independent review.
Positive
- $4.75 revised Lynx1 bid disclosed
- Paused R&D for BNC210 to conserve resources during review
- Multiple indications of interest; ~12 advanced to NDAs
- Licensing agreements generated tens of millions in revenue
Negative
- Lynx1 bid priced near estimated cash value, per company
- Electing dissident nominees could truncate strategic review
News Market Reaction
On the day this news was published, NEUP gained 1.43%, reflecting a mild positive market reaction.
Data tracked by StockTitan Argus on the day of publication.
Key Figures
Market Reality Check
Peers on Argus
Peers show mixed moves: AKTX up 4.33%, RNTX up 2.67%, while BOLD and KZR are down 2.54% and 0.79%, respectively. With no peers in momentum scanners and only one peer with news, trading in NEUP appears more company-specific than sector-driven.
Historical Context
| Date | Event | Sentiment | Move | Catalyst |
|---|---|---|---|---|
| Dec 04 | Bid response | Positive | +1.4% | Board criticizes reduced <b>$4.75</b> bid and highlights multiple competing interests. |
| Dec 01 | Proxy dispute | Neutral | -2.9% | Company counters Lynx1 narratives during ongoing proxy contest over board seats. |
| Nov 24 | Stockholder letter | Neutral | -0.7% | Letter to stockholders during contested proxy and strategic review process. |
| Nov 11 | Strategic review start | Positive | -0.2% | Launch of strategic review and disclosure of initial <b>$5.20</b> per-share Lynx1 bid. |
| Oct 27 | Rights plan | Negative | -27.4% | Adoption of limited-duration stockholder rights plan with <b>15%</b> ownership trigger. |
News around the strategic review and governance has produced mixed reactions, with sharp downside on the rights plan but modest moves around bid and proxy communications.
This announcement continues a series of governance and strategic review developments for Neuphoria. Since October 27, 2025, the company adopted a stockholder rights plan with a 15% trigger and later formally initiated a strategic review with H.C. Wainwright as advisor. An unsolicited $5.20 per-share bid from Lynx1 and a contested proxy process have dominated recent news. The current response to Lynx1’s reduced $4.75 bid fits into this ongoing effort to manage competing offers and protect the review process.
Market Pulse Summary
This announcement underscores Neuphoria’s intent to continue a structured strategic alternatives review while rejecting Lynx1’s reduced $4.75 per-share indication as inadequate. It highlights paused R&D on BNC210 in PTSD, existing licensing agreements, and a crowded field of potential counterparties. Recent history features a rights plan, an earlier $5.20 bid, and an active proxy contest. Investors may watch upcoming meeting outcomes and any revised proposals for clarity on ultimate deal terms and governance control.
Key Terms
strategic alternatives review financial
Phase 3 medical
non-disclosure agreement regulatory
proxy contest financial
proxy card financial
AI-generated analysis. Not financial advice.
Neuphoria Will Continue its Well-Planned Strategic Alternatives Review, Which has Garnered Significant Positive Interest
Urges Stockholders to Vote “FOR” BOTH of Neuphoria’s Nominees on the WHITE Proxy Card
BURLINGTON, Mass., Dec. 04, 2025 (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 dissident stockholder, Lynx1 Master Fund LP’s (“Lynx1”), revised indication of interest to acquire the Company.
Lynx1 Operating Outside Neuphoria’s Robust and Ongoing Strategic Alternatives Review Process
As previously announced, the Board – with assistance of its independent financial and legal advisors – is in the midst of a robust and comprehensive review of strategic alternatives to consider alternative assets, strategic pathways and/or to advance the Company’s promising pipeline program to maximize value for all stockholders. The Company has paused its research and development expenditures for BNC210 in PTSD and is evaluating all possibilities as part of the Company’s strategic review. This process is well underway and the Company has received substantial reciprocal interest from potential counterparties across a range of sectors. In addition, several parties have already engaged with the Company under confidentiality arrangements, and discussions are ongoing through the Company’s financial advisor, H.C. Wainwright & Co, and its independent legal advisors. The Board is continuing to evaluate all proposals, including the new unsolicited proposal submitted by Lynx1. The Board, in consultation with its advisors, will review Lynx1’s new proposal in the same manner that it reviews any other proposals received as part of its strategic alternative review process and subject it to all the same processes and procedures that apply to any other proposal – despite Lynx1’s seeming determination to operate outside that process, the only such party doing so at this time.
The Company believes it is important for stockholders to understand that the Company’s actions reflect a thoughtful and proactive strategy for the Company’s future—not a reactive one. A substantial amount of advanced planning for this strategic review was completed before the data readout of the AFFIRM-1 Phase 3 trial of BNC210 in SAD, which enabled the Company to launch the strategic review process expeditiously. The Company’s strategy has been built through meticulous work, including meetings with external stakeholders, comprehensive internal diligence, and constructive discussions with the Food and Drug Administration. The Board remains fully committed to executing this strategic review process, with the goal of delivering substantial value for all stockholders.
Lynx1’s Revised Bid Does Not Appropriately Value the Company
The Board has carefully evaluated Lynx1’s new unsolicited proposal. The new bid is lower than its initial bid at
While the Board remains open to all paths that enhance stockholder value, the Company will NOT pursue any transaction that undervalues the Company from a commercial perspective, ignores participants that form an important part of the Company’s stakeholders, and prematurely truncates and avoids the robust ongoing strategic review. Simply stated, Lynx1’s non-binding proposal does not present an attractive value, and certainly not one that would compel the Board to consider abandoning its ongoing strategic review process – especially given that the Company has already received a substantial number of competing indications of interest, with nearly a dozen that have already advanced to NDAs and separate process letter proposals. The Company will evaluate the Lynx1 proposal as part of its consideration of all the offers it has received – but not to the exclusion of other viable offers.
In addition, if Lynx1 succeeds in electing its nominees, their directors may favor Lynx1’s proposal, rather than objectively evaluating all proposals received. This creates a significant risk that superior, more value-enhancing, or better-aligned strategic opportunities may be disregarded or never fully considered. For this reason, we strongly urge you to stand firm with the Company’s Board by supporting the election of the Company’s existing highly qualified and experienced Board nominees—whose only interest is protecting and maximizing value for ALL our stockholders.
Revised Lynx1 Bid Does Not Consider our Complex Agreements
Lynx1 has not done sufficient diligence on the Company before submitting their new reduced price and reduced premium bid, as it significantly undervalues the Company’s potential based on its relationships, and by not conducting proper due diligence, Lynx1 fails to take into consideration the complex nature of Neuphoria’s existing contractual arrangements.
Lynx1 Complains About Not Receiving Special Treatment, While Acting Outside the Strategic Review Process
Neuphoria and its financial advisors have been diligently working to conduct a thorough and fair strategic review process, providing all interested parties with the same information and documentation. In fact, Lynx1 received the same non-disclosure agreement as all other interested parties and became quite upset that they were being asked to sign a typical non-disclosure agreement for a strategic review process seemingly because they feared it would prohibit them from continuing its self-interested proxy contest. Lynx1 returned comments to the Company on the non-disclosure agreement that were off market in that they entirely deleted the customary standstill provision, and in response the Company acting in good faith sent Lynx1 back a revised agreement that specifically exempted Lynx1’s proxy contest from the standstill provisions. The Company intends to be fair and treat all bidders in a similar fashion, including Lynx1, even though Lynx1 seems to be expecting special treatment due to their ongoing proxy contest.
In addition, by submitting a new and lower unsolicited bid, Lynx1 is trying to circumvent the Company’s ongoing strategic review process and inexplicably hoping to get preference over the other interested parties. The Company plans to stay the course and continue with their thorough strategic review process in order to meet their goal of maximizing stockholder value.
The Company therefore urges stockholders to vote “FOR” BOTH of Neuphoria’s nominees — Davies and Wilson — and vote “WITHHOLD” on both of Lynx1’s nominees on the WHITE proxy card TODAY. If you have any questions or need assistance voting please contact Sodali & Co at (203) 658-9400 or NEUP@investor.sodali.com.
Advisors
H.C. Wainwright & Co. is serving as financial advisor, and Rimon PC and Paul Hastings LLP are serving as legal counsel to Neuphoria. Sodali & Co is serving as proxy solicitor.
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