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[8-K] Anebulo Pharmaceuticals, Inc. Reports Material Event

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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 portare avanti 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 legato al raggiungimento di specifici traguardi, da utilizzare secondo un piano di sviluppo concordato.

Opus deve raggiungere determinati obiettivi di sviluppo; in caso contrario, o in presenza di altri Eventi Scatenanti della Licenza, le Parti Finanziatrici otterranno una licenza non esclusiva, mondiale e senza royalty sul programma. Opus avrà accesso reciproco ai dati generati e potrà negoziare l'esclusività, ma non potrà concedere a terzi una licenza esclusiva negli Stati Uniti durante il periodo 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, e include clausole standard di risoluzione per inadempienza o fallimento. L'accordo è divulgato ai sensi del Punto 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 retiniana hereditaria. Las Partes Financiadoras proporcionarán hasta 1,6 millones de dólares en capital no dilutivo basado en hitos, que debe usarse según un plan de desarrollo mutuamente acordado.

Opus debe cumplir con hitos específicos de desarrollo; en caso contrario, u otros Eventos Desencadenantes de la Licencia, las Partes Financiadoras obtendrán una licencia no exclusiva, mundial y libre de regalías sobre el programa. Opus tendrá acceso recíproco a los datos generados y podrá negociar exclusividad, pero no podrá otorgar una licencia exclusiva en EE. UU. a terceros durante el plazo sin el consentimiento de las Partes Financiadoras.

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

2025년 7월 22일, Opus Genetics(Nasdaq: IRD)는 Eyes on the Future 및 RDH12 Fund for Sight와 유전성 망막 퇴행 치료를 위한 RDH12 유전자 치료 프로그램을 발전시키기 위한 자금 지원 및 라이선스 계약을 체결했습니다. 자금 제공자는 상호 합의된 개발 계획에 따라 사용되어야 하는 마일스톤 기반의 비희석 자본 최대 160만 달러를 제공합니다.

Opus는 특정 개발 마일스톤을 달성해야 하며, 이를 달성하지 못하거나 기타 라이선스 발동 이벤트가 발생하면 자금 제공자는 프로그램에 대해 비독점적, 전 세계적, 로열티 없는 라이선스를 갖게 됩니다. Opus는 생성된 데이터에 상호 접근 권한을 가지며 독점권 협상을 할 수 있지만, 자금 제공자의 동의 없이 계약 기간 동안 제3자에게 미국 내 독점 라이선스를 부여할 수 없습니다.

계약은 (i) 트리거 이벤트 이전에 1a/2b상 시험에서 세 명의 환자에게 투여하거나, (ii) 규제 승인 후 첫 상업적 판매 시 종료되며, 위반 또는 파산 시 표준 해지 조항을 포함합니다. 계약 내용은 항목 1.01에 따라 공개되었으며, 관련 보도자료는 부록 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 progresser 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, conditionné à l'atteinte de jalons, devant être utilisé selon un plan de développement convenu mutuellement.

Opus doit atteindre des jalons spécifiques de développement ; en cas d'échec ou d'autres événements déclencheurs de licence, les parties financées obtiendront 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 accorder à un tiers une licence exclusive aux États-Unis pendant la durée sans le consentement des parties financées.

L'accord prend fin dès (i) la dose administrée à trois patients dans un essai de phase 1a/2b avant un événement déclencheur, ou (ii) la première vente commerciale après approbation réglementaire, et comprend des clauses standards 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; bei Nichterfüllung oder anderen Lizenz-Auslöseereignissen erhalten die Finanzierungspartner eine nicht-exklusive, weltweite, lizenzgebührenfreie Lizenz für das Programm. Opus erhält im Gegenzug Zugang zu den 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 bei (i) Dosierung von drei Patienten in einer Phase 1a/2b-Studie vor einem Auslöseereignis oder (ii) dem ersten kommerziellen Verkauf nach behördlicher Zulassung und enthält Standardkündigungsrechte bei Vertragsverletzung oder Insolvenz. Die Vereinbarung wird unter 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 portare avanti 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 legato al raggiungimento di specifici traguardi, da utilizzare secondo un piano di sviluppo concordato.

Opus deve raggiungere determinati obiettivi di sviluppo; in caso contrario, o in presenza di altri Eventi Scatenanti della Licenza, le Parti Finanziatrici otterranno una licenza non esclusiva, mondiale e senza royalty sul programma. Opus avrà accesso reciproco ai dati generati e potrà negoziare l'esclusività, ma non potrà concedere a terzi una licenza esclusiva negli Stati Uniti durante il periodo 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, e include clausole standard di risoluzione per inadempienza o fallimento. L'accordo è divulgato ai sensi del Punto 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 retiniana hereditaria. Las Partes Financiadoras proporcionarán hasta 1,6 millones de dólares en capital no dilutivo basado en hitos, que debe usarse según un plan de desarrollo mutuamente acordado.

Opus debe cumplir con hitos específicos de desarrollo; en caso contrario, u otros Eventos Desencadenantes de la Licencia, las Partes Financiadoras obtendrán una licencia no exclusiva, mundial y libre de regalías sobre el programa. Opus tendrá acceso recíproco a los datos generados y podrá negociar exclusividad, pero no podrá otorgar una licencia exclusiva en EE. UU. a terceros durante el plazo sin el consentimiento de las Partes Financiadoras.

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

2025년 7월 22일, Opus Genetics(Nasdaq: IRD)는 Eyes on the Future 및 RDH12 Fund for Sight와 유전성 망막 퇴행 치료를 위한 RDH12 유전자 치료 프로그램을 발전시키기 위한 자금 지원 및 라이선스 계약을 체결했습니다. 자금 제공자는 상호 합의된 개발 계획에 따라 사용되어야 하는 마일스톤 기반의 비희석 자본 최대 160만 달러를 제공합니다.

Opus는 특정 개발 마일스톤을 달성해야 하며, 이를 달성하지 못하거나 기타 라이선스 발동 이벤트가 발생하면 자금 제공자는 프로그램에 대해 비독점적, 전 세계적, 로열티 없는 라이선스를 갖게 됩니다. Opus는 생성된 데이터에 상호 접근 권한을 가지며 독점권 협상을 할 수 있지만, 자금 제공자의 동의 없이 계약 기간 동안 제3자에게 미국 내 독점 라이선스를 부여할 수 없습니다.

계약은 (i) 트리거 이벤트 이전에 1a/2b상 시험에서 세 명의 환자에게 투여하거나, (ii) 규제 승인 후 첫 상업적 판매 시 종료되며, 위반 또는 파산 시 표준 해지 조항을 포함합니다. 계약 내용은 항목 1.01에 따라 공개되었으며, 관련 보도자료는 부록 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 progresser 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, conditionné à l'atteinte de jalons, devant être utilisé selon un plan de développement convenu mutuellement.

Opus doit atteindre des jalons spécifiques de développement ; en cas d'échec ou d'autres événements déclencheurs de licence, les parties financées obtiendront 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 accorder à un tiers une licence exclusive aux États-Unis pendant la durée sans le consentement des parties financées.

L'accord prend fin dès (i) la dose administrée à trois patients dans un essai de phase 1a/2b avant un événement déclencheur, ou (ii) la première vente commerciale après approbation réglementaire, et comprend des clauses standards 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; bei Nichterfüllung oder anderen Lizenz-Auslöseereignissen erhalten die Finanzierungspartner eine nicht-exklusive, weltweite, lizenzgebührenfreie Lizenz für das Programm. Opus erhält im Gegenzug Zugang zu den 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 bei (i) Dosierung von drei Patienten in einer Phase 1a/2b-Studie vor einem Auslöseereignis oder (ii) dem ersten kommerziellen Verkauf nach behördlicher Zulassung und enthält Standardkündigungsrechte bei Vertragsverletzung oder Insolvenz. Die Vereinbarung wird unter Punkt 1.01 offengelegt; eine zugehörige Pressemitteilung ist als Anlage 99.1 beigefügt.

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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 23, 2025

 

 

 

ANEBULO PHARMACEUTICALS, INC

(Exact name of Registrant as Specified in Its Charter)

 

 

 

Delaware   001-40388   85-1170950

(State or Other Jurisdiction

of Incorporation)

 

(Commission

File Number)

 

(IRS Employer

Identification No.)

 

Anebulo Pharmaceuticals, Inc.

1017 Ranch Road 620 South, Suite 107

Lakeway, TX

  78734
(Address of Principal Executive Offices)   (Zip Code)

 

Registrant’s Telephone Number, Including Area Code: (512) 598-0931

 

Not Applicable

(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, $.0.001 par value per share   ANEB   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 8.01 Other Events.

 

On July 23, 2025, Anebulo Pharmaceuticals, Inc., a Delaware corporation (the “Company” or “Anebulo”) announced that a Special Committee of independent directors has recommended, and its Board of Directors (the “Board”) has approved, as part of a going private transaction, an amendment (the “Amendment”) to the Company’s Second Amended and Restated Certificate of Incorporation (the “Certificate of Incorporation”), to effect a reverse stock split (the “Reverse Stock Split”) of the Company’s issued and outstanding shares of common stock, par value $0.001 per share (the “Common Stock”), subject to obtaining the requisite approval of the Company’s stockholders at a Special Meeting of Stockholders to be held for that purpose, which is currently expected to occur on August 22, 2025.

 

Specifically, the Board approved an Amendment to the Certificate of Incorporation to effect a Reverse Stock Split of the Company’s issued and outstanding Common Stock, including stock held by the Company as treasury shares, at a ratio (the “Stock Split Ratio”) of not less than 1-for-2,500 and not greater than 1-for-7,500 (the “Range”), with the exact Stock Split Ratio to be set within the Range without further approval or authorization of the Company’s stockholders at the discretion of the Board and included in a public announcement, subject to the authority of the Board to abandon the Amendment. The Reverse Stock Split is being undertaken as part of the Company’s plan to go private and terminate the registration of the Common Stock under Section 12(b) of the Securities Exchange Act of 1934, as amended, and suspend the Company’s duty to file periodic reports and other information with the Securities and Exchange Commission (the “SEC”) under Section 13(a) thereunder, and to delist the Common Stock from The Nasdaq Stock Market. In order to do so the Company must reduce the number of record holders of its Common Stock to below 300, which is the level at or above which the Company is required to file public reports with the SEC.

 

The Board may abandon the Reverse Stock Split at any time prior to the filing and effectiveness of the Amendment to the Company’s Certificate Of Incorporation, even after stockholder approval, if the Board determines that the Reverse Stock Split is no longer in the best interests of the Company or its stockholders.

 

If the Reverse Stock Split Proposal is approved and the Reverse Stock Split effected (i) a stockholder of record owning fewer than a minimum number of shares of Common Stock at the effective time of the Reverse Stock Split, which, depending on the Stock Split Ratio chosen by the Board, would be between 2,500 and 7,500 (the “Minimum Number”), will be entitled to receive only the cash payment of $3.50 multiplied by the number of shares owned by such stockholder immediately before the Reverse Stock Split, without interest (the “Cash Payment”), will no longer be a stockholder, will no longer have any ownership interest in the Company, and will cease to participate in the potential appreciation in the value of the Common Stock or the Company’s future distributions to stockholders, if any; and (ii) a stockholder of record owning more than the Minimum Number of shares immediately prior to the effective time of the Reverse Stock Split will continue to hold one share of Common Stock for every integer multiple of the Minimum Number of shares of Common Stock such stockholder owns immediately prior to the effective time of the Reverse Stock Split, will remain a stockholder of the Company and will receive a Cash Payment for such stockholder’s fractional share interests resulting from the Reverse Stock Split, if any. The Reverse Stock Split, together with the Cash Payments to stockholders in lieu of fractional shares, is referred to as the “Transaction.”

 

-2-
 

 

The terms and contemplated timeline of the Transaction, including the factors considered by the Special Committee in recommending, and the Board in approving, the Transaction are set forth in a preliminary proxy statement filed by the Company on July 23, 2025 and a transaction statement on Schedule 13E-3 filed by the Company on July 23, 2025.

 

On July 23, 2025, the Company issued a press release regarding the Transaction. A copy of the press release is filed as Exhibit 99.1 to this Current Report on Form 8-K.

 

Additional Information and Where to Find It

 

THIS CURRENT REPORT ON FORM 8-K IS ONLY A BRIEF DESCRIPTION OF THE TRANSACTION. IT IS NOT A REQUEST FOR OR SOLICITATION OF A PROXY OR AN OFFER TO ACQUIRE OR SELL ANY SHARES OF COMMON STOCK. THE COMPANY HAS FILED A PRELIMINARY PROXY STATEMENT AND OTHER REQUIRED MATERIALS, INCLUDING A PRELIMINARY SCHEDULE 13E-3, WITH THE SEC CONCERNING THE PROPOSED STOCK SPLIT. THE COMPANY INTENDS TO FILE A DEFINITIVE PROXY STATEMENT, AND OTHER REQUIRED MATERIALS, INCLUDING A SCHEDULE 13E-3, WITH THE SEC. A COPY OF ALL FINAL PROXY MATERIALS WILL BE SENT TO STOCKHOLDERS PRIOR TO A SPECIAL MEETING OF STOCKHOLDERS AT WHICH THE COMPANY’S STOCKHOLDERS WILL BE ASKED TO VOTE ON THE PROPOSALS DESCRIBED IN THE MATERIALS PROVIDED BY THE COMPANY. THE COMPANY URGES ALL STOCKHOLDERS TO READ THE DEFINITIVE PROXY STATEMENT WHEN IT BECOMES AVAILABLE, AS WELL AS ALL OTHER RELEVANT DOCUMENTS FILED WITH THE SEC, BECAUSE THOSE DOCUMENTS WILL INCLUDE IMPORTANT INFORMATION. A FREE COPY OF ALL MATERIALS THE COMPANY FILES WITH THE SEC, INCLUDING THE COMPANY’S SCHEDULE 13E-3 AND PROXY STATEMENT, WILL BE AVAILABLE AT NO COST ON THE SEC’S WEBSITE AT WWW.SEC.GOV. WHEN THOSE DOCUMENTS BECOME AVAILABLE, THE PROXY STATEMENT AND OTHER DOCUMENTS FILED BY THE COMPANY MAY ALSO BE OBTAINED WITHOUT CHARGE BY DIRECTING A REQUEST TO ANEBULO PHARMACEUTICALS, INC., 1017 RANCH ROAD 620 SOUTH, SUITE 107, LAKEWAY, TEXAS 78734, ATTENTION: SECRETARY.

 

Anebulo and its directors and executive officers may be deemed to be participants in the solicitation of proxies in connection with the proposed transaction. Information concerning such participants is set forth in the preliminary proxy statement for Anebulo’s special meeting of stockholders, which was filed with the SEC on Schedule 14A on July 23, 2025. To the extent that holdings of Anebulo’s securities change, such changes will be reflected on Statements of Change in Ownership on Form 4 filed with the SEC. Additional information regarding the interests of such participants in the solicitation of proxies in connection with the proposed transaction, if any, will be included in the definitive proxy statement to be filed by Anebulo with the SEC in connection with the proposed transaction

 

Item 9.01 Financial Statements and Exhibits.

 

(d) Exhibits

 

The following exhibit is filed with this Current Report on Form 8-K:

 

Exhibit

Number

  Description
99.1   Press Release dated July 23, 2025
104   Cover Page of Interactive Data File (embedded within the Inline XBRL document).

 

-3-
 

 

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.

 

  ANEBULO PHARMACEUTICALS, INC.
     
Date: July 23, 2025 By: /s/ Richard Anthony Cunningham
    Richard Anthony Cunningham
    Chief Executive Officer (Principal Executive Officer)

 

-4-

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.
Anebulo Pharmaceuticals Inc

NASDAQ:ANEB

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