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[8-K] Scilex Holding Company Warrant Reports Material Event

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8-K
Rhea-AI Filing Summary

On 22 Jul 2025 Opus Genetics (Nasdaq: IRD) executed a Funding & License Agreement with Eyes on the Future and RDH12 Fund for Sight to advance its RDH12 gene-therapy program for inherited retinal degeneration. The Funding Parties will supply up to $1.6 million in milestone-driven, non-dilutive capital that must be used under a mutually agreed development plan.

Opus must meet specific development milestones; failure to do so or other License Trigger Events would give the Funding Parties a non-exclusive, worldwide, royalty-free license to the program. Opus would gain reciprocal access to the generated data and may negotiate for exclusivity, but it cannot grant a third party an exclusive U.S. license during the term without Funding Party consent.

The agreement ends upon (i) dosing three patients in a Phase 1a/2b trial before a trigger event, or (ii) first commercial sale after regulatory approval, and includes standard termination for breach or bankruptcy. The deal is disclosed under Item 1.01; a related press release is furnished as Exhibit 99.1.

Il 22 luglio 2025 Opus Genetics (Nasdaq: IRD) ha stipulato un Accordo di Finanziamento e Licenza con Eyes on the Future e RDH12 Fund for Sight per avanzare il suo programma di terapia genica RDH12 per la degenerazione retinica ereditaria. Le Parti Finanziatrici forniranno fino a 1,6 milioni di dollari in capitale non diluitivo basato su traguardi, da utilizzare secondo un piano di sviluppo concordato reciprocamente.

Opus deve raggiungere specifici traguardi di sviluppo; il mancato raggiungimento o altri Eventi Scatenanti della Licenza conferirebbero alle Parti Finanziatrici una licenza non esclusiva, mondiale e senza royalty sul programma. Opus otterrà accesso reciproco ai dati generati e potrà negoziare l'esclusività, ma non potrà concedere a terzi una licenza esclusiva negli Stati Uniti durante la durata senza il consenso delle Parti Finanziatrici.

L'accordo termina al verificarsi di (i) somministrazione a tre pazienti in uno studio di Fase 1a/2b prima di un evento scatenante, o (ii) prima vendita commerciale dopo l'approvazione regolatoria, includendo clausole standard di risoluzione per inadempienza o fallimento. L'accordo è reso noto ai sensi dell'Articolo 1.01; un comunicato stampa correlato è fornito come Allegato 99.1.

El 22 de julio de 2025, Opus Genetics (Nasdaq: IRD) firmó un Acuerdo de Financiamiento y Licencia con Eyes on the Future y RDH12 Fund for Sight para avanzar en su programa de terapia génica RDH12 para la degeneración retinal hereditaria. Las Partes Financiadoras proporcionarán hasta 1,6 millones de dólares en capital no dilutivo basado en hitos, que debe usarse bajo un plan de desarrollo mutuamente acordado.

Opus debe cumplir con hitos específicos de desarrollo; el incumplimiento o la ocurrencia de otros Eventos Desencadenantes de la Licencia otorgarían a las Partes Financiadoras una licencia no exclusiva, mundial y libre de regalías sobre el programa. Opus obtendrá acceso recíproco a los datos generados y podrá negociar la exclusividad, pero no podrá conceder una licencia exclusiva en EE. UU. a terceros durante el término sin el consentimiento de las Partes Financiadoras.

El acuerdo finaliza al (i) administrar dosis a tres pacientes en un ensayo de Fase 1a/2b antes de un evento desencadenante, o (ii) la primera venta comercial tras la aprobación regulatoria, e incluye terminación estándar por incumplimiento o bancarrota. El acuerdo se divulga conforme al Punto 1.01; un comunicado de prensa relacionado se presenta como Anexo 99.1.

2025년 7월 22일, Opus Genetics(Nasdaq: IRD)는 Eyes on the Future 및 RDH12 Fund for Sight와 유전성 망막 퇴행을 위한 RDH12 유전자 치료 프로그램을 진전시키기 위한 자금 지원 및 라이선스 계약을 체결했습니다. 자금 제공 당사자들은 상호 합의된 개발 계획에 따라 사용되어야 하는 160만 달러까지의 마일스톤 기반 비희석 자본을 제공할 예정입니다.

Opus는 특정 개발 마일스톤을 충족해야 하며, 이를 달성하지 못하거나 다른 라이선스 발동 이벤트가 발생할 경우 자금 제공 당사자들은 해당 프로그램에 대해 비독점적, 전 세계적, 로열티 없는 라이선스를 갖게 됩니다. Opus는 생성된 데이터에 상호 접근할 수 있으며 독점권 협상을 할 수 있으나, 자금 제공 당사자의 동의 없이 계약 기간 중 제3자에게 미국 내 독점 라이선스를 부여할 수 없습니다.

계약은 (i) 트리거 이벤트 이전에 1a/2b상 시험에서 세 명의 환자 투여 완료 시 또는 (ii) 규제 승인 후 첫 상업 판매 시 종료되며, 위반 또는 파산 시 표준 해지 조항도 포함합니다. 이 계약은 항목 1.01에 따라 공시되었으며, 관련 보도자료는 부속서 99.1로 제공됩니다.

Le 22 juillet 2025, Opus Genetics (Nasdaq : IRD) a conclu un accord de financement et de licence avec Eyes on the Future et RDH12 Fund for Sight afin de faire avancer son programme de thérapie génique RDH12 pour la dégénérescence rétinienne héréditaire. Les parties financées fourniront jusqu'à 1,6 million de dollars de capital non dilutif basé sur des jalons, devant être utilisé selon un plan de développement mutuellement convenu.

Opus doit atteindre des jalons de développement spécifiques ; le non-respect ou d'autres événements déclencheurs de licence donneraient aux parties financées une licence non exclusive, mondiale et sans redevance sur le programme. Opus bénéficiera d'un accès réciproque aux données générées et pourra négocier une exclusivité, mais ne pourra pas accorder à un tiers une licence exclusive aux États-Unis pendant la durée sans le consentement des parties financées.

L'accord prend fin lors de (i) l'administration à trois patients dans un essai de phase 1a/2b avant un événement déclencheur, ou (ii) la première vente commerciale après l'approbation réglementaire, et inclut des clauses standard de résiliation en cas de manquement ou de faillite. L'accord est divulgué conformément à l'article 1.01 ; un communiqué de presse associé est fourni en annexe 99.1.

Am 22. Juli 2025 schloss Opus Genetics (Nasdaq: IRD) eine Finanzierungs- und Lizenzvereinbarung mit Eyes on the Future und RDH12 Fund for Sight ab, um sein RDH12-Gentherapieprogramm für erbliche Netzhautdegeneration voranzutreiben. Die Finanzierungspartner stellen bis zu 1,6 Millionen US-Dollar an meilensteinabhängigem, nicht verwässerndem Kapital bereit, das gemäß einem gemeinsam vereinbarten Entwicklungsplan verwendet werden muss.

Opus muss bestimmte Entwicklungsmeilensteine erreichen; das Nichterreichen oder andere Lizenz-Auslöseereignisse würden den Finanzierungspartnern eine nicht-exklusive, weltweite, lizenzgebührenfreie Lizenz am Programm einräumen. Opus erhält im Gegenzug Zugriff auf die generierten Daten und kann Exklusivität verhandeln, darf jedoch ohne Zustimmung der Finanzierungspartner während der Laufzeit keine exklusive US-Lizenz an Dritte vergeben.

Die Vereinbarung endet, wenn (i) vor einem Auslöseereignis drei Patienten in einer Phase 1a/2b-Studie behandelt wurden oder (ii) der erste kommerzielle Verkauf nach behördlicher Zulassung erfolgt, und umfasst Standardkündigungen bei Vertragsbruch oder Insolvenz. Die Vereinbarung wird gemäß Punkt 1.01 offengelegt; eine zugehörige Pressemitteilung ist als Anlage 99.1 beigefügt.

Positive
  • $1.6 M in non-dilutive funding strengthens cash position for early RDH12 development.
  • External stakeholders’ participation validates scientific approach and may attract further support.
Negative
  • Funding amount is relatively small and unlikely to cover later-stage clinical costs.
  • Failure to meet milestones could trigger a royalty-free license transfer, eroding future exclusivity and value.
  • Agreement restricts out-licensing in the U.S., limiting strategic and M&A flexibility.

Insights

TL;DR – $1.6 M non-dilutive cash aids pipeline, but milestone slippage risks loss of exclusivity.

The agreement provides modest yet helpful capital without share dilution, signalling external confidence in Opus’s RDH12 asset. However, the small amount will cover only early work; investors should focus on Opus’s ability to hit the milestone of dosing three patients in Phase 1a/2b. Missing that or other trigger events hands development rights to the funders, reducing Opus’s economic upside. Restrictions on out-licensing also limit strategic optionality. Overall impact is balanced: slight financial positive, offset by execution risk.

TL;DR – Conditional license clauses increase IP risk if diligence falters.

The royalty-free, global, non-exclusive license that activates upon a trigger event is unusually generous to the funders and could undermine Opus’s bargaining power with future partners. While Opus keeps a back-license and negotiation rights, any lapse in diligence could erode exclusivity and future revenue streams. The contractual bar on granting exclusive U.S. licenses without consent further narrows strategic flexibility. Investors should monitor compliance closely.

Il 22 luglio 2025 Opus Genetics (Nasdaq: IRD) ha stipulato un Accordo di Finanziamento e Licenza con Eyes on the Future e RDH12 Fund for Sight per avanzare il suo programma di terapia genica RDH12 per la degenerazione retinica ereditaria. Le Parti Finanziatrici forniranno fino a 1,6 milioni di dollari in capitale non diluitivo basato su traguardi, da utilizzare secondo un piano di sviluppo concordato reciprocamente.

Opus deve raggiungere specifici traguardi di sviluppo; il mancato raggiungimento o altri Eventi Scatenanti della Licenza conferirebbero alle Parti Finanziatrici una licenza non esclusiva, mondiale e senza royalty sul programma. Opus otterrà accesso reciproco ai dati generati e potrà negoziare l'esclusività, ma non potrà concedere a terzi una licenza esclusiva negli Stati Uniti durante la durata senza il consenso delle Parti Finanziatrici.

L'accordo termina al verificarsi di (i) somministrazione a tre pazienti in uno studio di Fase 1a/2b prima di un evento scatenante, o (ii) prima vendita commerciale dopo l'approvazione regolatoria, includendo clausole standard di risoluzione per inadempienza o fallimento. L'accordo è reso noto ai sensi dell'Articolo 1.01; un comunicato stampa correlato è fornito come Allegato 99.1.

El 22 de julio de 2025, Opus Genetics (Nasdaq: IRD) firmó un Acuerdo de Financiamiento y Licencia con Eyes on the Future y RDH12 Fund for Sight para avanzar en su programa de terapia génica RDH12 para la degeneración retinal hereditaria. Las Partes Financiadoras proporcionarán hasta 1,6 millones de dólares en capital no dilutivo basado en hitos, que debe usarse bajo un plan de desarrollo mutuamente acordado.

Opus debe cumplir con hitos específicos de desarrollo; el incumplimiento o la ocurrencia de otros Eventos Desencadenantes de la Licencia otorgarían a las Partes Financiadoras una licencia no exclusiva, mundial y libre de regalías sobre el programa. Opus obtendrá acceso recíproco a los datos generados y podrá negociar la exclusividad, pero no podrá conceder una licencia exclusiva en EE. UU. a terceros durante el término sin el consentimiento de las Partes Financiadoras.

El acuerdo finaliza al (i) administrar dosis a tres pacientes en un ensayo de Fase 1a/2b antes de un evento desencadenante, o (ii) la primera venta comercial tras la aprobación regulatoria, e incluye terminación estándar por incumplimiento o bancarrota. El acuerdo se divulga conforme al Punto 1.01; un comunicado de prensa relacionado se presenta como Anexo 99.1.

2025년 7월 22일, Opus Genetics(Nasdaq: IRD)는 Eyes on the Future 및 RDH12 Fund for Sight와 유전성 망막 퇴행을 위한 RDH12 유전자 치료 프로그램을 진전시키기 위한 자금 지원 및 라이선스 계약을 체결했습니다. 자금 제공 당사자들은 상호 합의된 개발 계획에 따라 사용되어야 하는 160만 달러까지의 마일스톤 기반 비희석 자본을 제공할 예정입니다.

Opus는 특정 개발 마일스톤을 충족해야 하며, 이를 달성하지 못하거나 다른 라이선스 발동 이벤트가 발생할 경우 자금 제공 당사자들은 해당 프로그램에 대해 비독점적, 전 세계적, 로열티 없는 라이선스를 갖게 됩니다. Opus는 생성된 데이터에 상호 접근할 수 있으며 독점권 협상을 할 수 있으나, 자금 제공 당사자의 동의 없이 계약 기간 중 제3자에게 미국 내 독점 라이선스를 부여할 수 없습니다.

계약은 (i) 트리거 이벤트 이전에 1a/2b상 시험에서 세 명의 환자 투여 완료 시 또는 (ii) 규제 승인 후 첫 상업 판매 시 종료되며, 위반 또는 파산 시 표준 해지 조항도 포함합니다. 이 계약은 항목 1.01에 따라 공시되었으며, 관련 보도자료는 부속서 99.1로 제공됩니다.

Le 22 juillet 2025, Opus Genetics (Nasdaq : IRD) a conclu un accord de financement et de licence avec Eyes on the Future et RDH12 Fund for Sight afin de faire avancer son programme de thérapie génique RDH12 pour la dégénérescence rétinienne héréditaire. Les parties financées fourniront jusqu'à 1,6 million de dollars de capital non dilutif basé sur des jalons, devant être utilisé selon un plan de développement mutuellement convenu.

Opus doit atteindre des jalons de développement spécifiques ; le non-respect ou d'autres événements déclencheurs de licence donneraient aux parties financées une licence non exclusive, mondiale et sans redevance sur le programme. Opus bénéficiera d'un accès réciproque aux données générées et pourra négocier une exclusivité, mais ne pourra pas accorder à un tiers une licence exclusive aux États-Unis pendant la durée sans le consentement des parties financées.

L'accord prend fin lors de (i) l'administration à trois patients dans un essai de phase 1a/2b avant un événement déclencheur, ou (ii) la première vente commerciale après l'approbation réglementaire, et inclut des clauses standard de résiliation en cas de manquement ou de faillite. L'accord est divulgué conformément à l'article 1.01 ; un communiqué de presse associé est fourni en annexe 99.1.

Am 22. Juli 2025 schloss Opus Genetics (Nasdaq: IRD) eine Finanzierungs- und Lizenzvereinbarung mit Eyes on the Future und RDH12 Fund for Sight ab, um sein RDH12-Gentherapieprogramm für erbliche Netzhautdegeneration voranzutreiben. Die Finanzierungspartner stellen bis zu 1,6 Millionen US-Dollar an meilensteinabhängigem, nicht verwässerndem Kapital bereit, das gemäß einem gemeinsam vereinbarten Entwicklungsplan verwendet werden muss.

Opus muss bestimmte Entwicklungsmeilensteine erreichen; das Nichterreichen oder andere Lizenz-Auslöseereignisse würden den Finanzierungspartnern eine nicht-exklusive, weltweite, lizenzgebührenfreie Lizenz am Programm einräumen. Opus erhält im Gegenzug Zugriff auf die generierten Daten und kann Exklusivität verhandeln, darf jedoch ohne Zustimmung der Finanzierungspartner während der Laufzeit keine exklusive US-Lizenz an Dritte vergeben.

Die Vereinbarung endet, wenn (i) vor einem Auslöseereignis drei Patienten in einer Phase 1a/2b-Studie behandelt wurden oder (ii) der erste kommerzielle Verkauf nach behördlicher Zulassung erfolgt, und umfasst Standardkündigungen bei Vertragsbruch oder Insolvenz. Die Vereinbarung wird gemäß Punkt 1.01 offengelegt; eine zugehörige Pressemitteilung ist als Anlage 99.1 beigefügt.

Scilex Holding Co false 0001820190 0001820190 2025-07-22 2025-07-22 0001820190 us-gaap:CommonStockMember 2025-07-22 2025-07-22 0001820190 us-gaap:WarrantMember 2025-07-22 2025-07-22
 
 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

 

FORM 8-K

 

 

CURRENT REPORT

PURSUANT TO SECTION 13 OR 15(d)

OF THE SECURITIES EXCHANGE ACT OF 1934

Date of Report (Date of earliest event reported): July 22, 2025

 

 

SCILEX HOLDING COMPANY

(Exact name of registrant as specified in its charter)

 

 

 

Delaware   001-39852   92-1062542

(State or other jurisdiction

of incorporation)

 

(Commission

File Number)

 

(IRS Employer

Identification No.)

960 San Antonio Road, Palo Alto, California, 94303

(Address of principal executive offices, including zip code)

Registrant’s telephone number, including area code: (650) 516-4310

N/A

(Former name or former address, if changed since last report)

 

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

 

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

 

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

 

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act

 

Title of each class

 

Trading
Symbol(s)

 

Name of each exchange
on which registered

Common stock, par value $0.0001 per share   SCLX   The Nasdaq Stock Market LLC
Warrants to purchase common stock at an exercise price of $402.50 per share   SCLXW   The Nasdaq Stock Market LLC

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. 

 

 
 


Item 1.01.

Entry into a Material Definitive Agreement.

Amendment to Merger Agreement

As previously disclosed by Scilex Holding Company (the “Company”), Semnur Pharmaceuticals, Inc. (“Semnur”), a Delaware corporation and wholly owned subsidiary of the Company, entered into an agreement and plan of merger (as amended by Amendment No. 1 to the Agreement and Plan of Merger, dated April 16, 2025, the “Merger Agreement”) with Denali Capital Acquisition Corp., a Cayman Islands exempted company (“Denali” or “Parent”), and Denali Merger Sub Inc., a Delaware corporation and wholly owned subsidiary of Denali (“Merger Sub”), pursuant to which, among other things, Merger Sub will merge with and into Semnur with Semnur surviving the merger as a wholly owned subsidiary of Denali (the “Merger”). The Merger and the other transactions contemplated by the Merger Agreement are hereinafter referred to as the “Business Combination”. All capitalized terms used and not otherwise defined herein shall have the meanings set forth in Amendment No. 2 (as defined below) and the Merger Agreement.

On July 22, 2025, Semnur entered into Amendment No. 2 to the Merger Agreement with Denali and Merger Sub (“Amendment No. 2”). Amendment No. 2 amends the Merger Agreement to, among other things, modify the definitions of the “Exchange Ratio” and “Merger Consideration” to facilitate the issuance of additional shares of common stock of Semnur prior to the closing of the Business Combination in connection with any potential private placement financing or for issuance to advisors and other service providers for services rendered and maintain the 1.25-to-1 exchange ratio.

The foregoing description of Amendment No. 2 does not purport to be complete and is qualified in its entirety by reference to Amendment No. 2, a copy of which is filed with this Current Report on Form 8-K as Exhibit 2.1 hereto and is incorporated herein by reference.

Additional Information

In connection with the Business Combination, Denali filed with the SEC a Registration Statement on Form S-4 (the “Denali Registration Statement”), which includes a preliminary prospectus and preliminary proxy statement. Denali will mail a definitive proxy statement/final prospectus and other relevant documents to its shareholders. This communication is not a substitute for the Denali Registration Statement, the definitive proxy statement/final prospectus or any other document that Denali will send to its shareholders in connection with the Business Combination. Investors and security holders of Denali are advised to read the proxy statement/prospectus in connection with Denali’s solicitation of proxies for its extraordinary general meeting of shareholders to be held to approve the Business Combination (and related matters) because the proxy statement/prospectus contains important information about the Business Combination and the parties to the Business Combination. The definitive proxy statement/final prospectus will be mailed to shareholders of Denali as of a record date to be established for voting on the Business Combination. Shareholders will also be able to obtain copies of the proxy statement/prospectus, without charge, once available, at the SEC’s website www.sec.gov or by directing a request to: 437 Madison Avenue, 27th Floor, New York, New York 10022.

Participants in the Solicitation

Denali, Semnur and their respective directors, executive officers, other members of management and employees, under SEC rules, may be deemed to be participants in the solicitation of proxies of Denali’s shareholders in connection with the Business Combination. Investors and security holders may obtain more detailed information regarding the names and interests in the Business Combination of Denali’s directors and officers in Denali’s filings with the SEC, including the Denali Registration Statement filed with the SEC by Denali, which includes the proxy statement of Denali for the Business Combination, and such information and names of Semnur’s directors and executive officers are also included in the Denali Registration Statement filed with the SEC by Denali, which includes the proxy statement of Denali for the Business Combination.

 

2


Forward-Looking Statements

This Current Report on Form 8-K includes forward-looking statements that involve risks and uncertainties. Forward-looking statements are statements that are not historical facts and may be accompanied by words that convey projected future events or outcomes, such as “believe,” “may,” “will,” “estimate,” “continue,” “anticipate,” “intend,” “expect,” “should,” “would,” “plan,” “predict,” “potential,” “seem,” “seek,” “future,” “outlook” or variations of such words or by expressions of similar meaning. These forward-looking statements include, but are not limited to, statements regarding future events, the Business Combination between Semnur and Denali, the estimated or anticipated future results and benefits of the combined company following the Business Combination, including the likelihood and ability of the parties to successfully consummate the Business Combination, future opportunities for the combined company, and other statements that are not historical facts. These statements are based on the current expectations of management of the Company, Semnur and Denali and are not predictions of actual performance. These forward-looking statements are provided for illustrative purposes only and are not intended to serve as, and must not be relied on, by any investor as a guarantee, an assurance, a prediction or a definitive statement of fact or probability. Actual events and circumstances are difficult or impossible to predict and will differ from assumptions. Many actual events and circumstances are beyond the control of the Company, Semnur and Denali. These statements are subject to a number of risks and uncertainties regarding the Company’s, Semnur’s and Denali’s businesses and the Business Combination, and actual results may differ materially. These risks and uncertainties include, but are not limited to, general economic, political and business conditions; the inability of the parties to consummate the Business Combination or the occurrence of any event, change or other circumstances that could give rise to the termination of the Merger Agreement; the outcome of any legal proceedings that may be instituted against the parties following the announcement of the Business Combination; the receipt of an unsolicited offer from another party for an alternative business transaction that could interfere with the Business Combination; the risk that the approval of the stockholders of Semnur or the shareholders of Denali for the potential transaction is not obtained; failure to realize the anticipated benefits of the Business Combination, including as a result of a delay in consummating the potential transaction or difficulty in integrating the businesses of Semnur or Denali; the risk that the Business Combination disrupts current plans and operations as a result of the announcement and consummation of the Business Combination; the ability of the combined company to grow and manage growth profitably and retain its key employees; the amount of redemption requests made by Denali’s shareholders; the inability to obtain financing; the inability to obtain or maintain the listing of the post-acquisition company’s securities on Nasdaq or OTC Markets following the Business Combination; and costs related to the Business Combination. There may be additional risks that Semnur and the Company presently do not know or that Semnur or the Company currently believe are immaterial that could also cause actual results to differ from those contained in the forward-looking statements. In addition, forward-looking statements provide Semnur’s, the Company’s and Denali’s expectations, plans or forecasts of future events and views as of the date of this communication. Semnur and the Company anticipate that subsequent events and developments will cause such assessments to change. However, while Semnur and the Company may elect to update these forward-looking statements at some point in the future, each of Semnur and the Company specifically disclaim any obligation to do so. These forward-looking statements should not be relied upon as representing Semnur’s or the Company’s assessments as of any date subsequent to the date of this communication. Accordingly, undue reliance should not be placed upon the forward-looking statements.

Disclaimer

This communication is for informational purposes only and is neither an offer to purchase, nor a solicitation of an offer to sell, subscribe for or buy any securities or the solicitation of any vote in any jurisdiction pursuant to the Business Combination or otherwise, nor shall there be any sale, issuance or transfer of securities in any jurisdiction in contravention of applicable law. No offer of securities shall be made except by means of a prospectus meeting the requirements of Section 10 of the Securities Act.

 

3


Item 9.01.

Financial Statements and Exhibits.

(d) Exhibits.

 

Exhibit
Number

  

Description

2.1    Amendment No. 2 to Agreement and Plan of Merger, dated as of July 22, 2025, by and among Denali Capital Acquisition Corp., Denali Merger Sub Inc. and Semnur Pharmaceuticals, Inc.
104    Cover Page Interactive Data File, formatted in Inline Extensible Business Reporting Language (iXBRL).

 

4


SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

SCILEX HOLDING COMPANY
By:   /s/ Jaisim Shah
Name:   Jaisim Shah
Title:   Chief Executive Officer & President

Date: July 23, 2025

 

5

FAQ

How much funding does Opus Genetics (IRD) receive under the RDH12 agreement?

Up to $1.6 million in milestone-based, non-dilutive financing.

What happens if Opus misses development milestones for RDH12?

The Funding Parties can invoke a non-exclusive, worldwide, royalty-free license to develop the program themselves.

Are there restrictions on Opus licensing RDH12 to other partners?

Yes. Opus cannot grant a third party an exclusive U.S. license during the agreement term without Funding Party consent.

When does the agreement with Eyes on the Future and RDH12 Fund for Sight terminate?

Upon dosing three patients in a Phase 1a/2b trial before a trigger event, first commercial sale post-approval, or standard breach/bankruptcy termination.

Is the information in the 8-K considered filed or furnished?

Item 1.01 is filed; Item 7.01 and Exhibit 99.1 are furnished and not deemed filed under Section 18 of the Exchange Act.
Scilex Holding Company

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Biological Products, (no Disgnostic Substances)
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