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[8-K] Aimfinity Investment Corp. I Unit Reports Material Event

Filing Impact
(Moderate)
Filing Sentiment
(Neutral)
Form Type
8-K
Rhea-AI Filing Summary

On June 30, 2025 INmune Bio, Inc. (NASDAQ: INMB) filed a Form 8-K under Item 8.01 to report a material corporate event. The company issued a press release disclosing topline results from its Phase 2 MINDFuL trial of XPro™ in patients with early Alzheimer’s disease. The 8-K itself does not include numerical efficacy or safety data but incorporates the press release (Exhibit 99.1) and an updated corporate presentation (Exhibit 99.2) by reference, directing investors to those documents for detailed findings and development strategy.

The disclosure marks a critical clinical milestone for INmune Bio because XPro is its lead asset in a large, high-value neuro-degenerative market. While the filing confirms trial completion and data availability, the absence of quantitative outcomes prevents immediate assessment of clinical success, regulatory pathway, or commercial outlook. Investors will need to review the accompanying exhibits—or await further commentary from management—to evaluate next-step implications such as Phase 3 design, partnership interest, or funding requirements.

No financial statements, earnings figures, or transactional details accompanied the filing. The company left all boxes related to Rule 425, proxy solicitation, and tender-offer communications unchecked, indicating that the 8-K is confined to the scientific update. Overall, the event is potentially material but its impact—positive or negative—remains indeterminate until the underlying data are scrutinised.

Il 30 giugno 2025, INmune Bio, Inc. (NASDAQ: INMB) ha presentato un modulo 8-K ai sensi dell'Elemento 8.01 per comunicare un evento aziendale rilevante. La società ha diffuso un comunicato stampa che annuncia i risultati preliminari della Fase 2 dello studio MINDFuL su XPro™ in pazienti con Alzheimer precoce. Il modulo 8-K non include dati numerici sull'efficacia o sicurezza, ma integra il comunicato stampa (Allegato 99.1) e una presentazione aziendale aggiornata (Allegato 99.2) tramite riferimento, indirizzando gli investitori a tali documenti per approfondimenti e strategie di sviluppo.

Questa divulgazione rappresenta una tappa clinica fondamentale per INmune Bio, poiché XPro è il suo principale prodotto in un mercato neurodegenerativo ampio e di grande valore. Sebbene la comunicazione confermi il completamento dello studio e la disponibilità dei dati, l'assenza di risultati quantitativi impedisce una valutazione immediata del successo clinico, del percorso regolatorio o delle prospettive commerciali. Gli investitori dovranno consultare gli allegati o attendere ulteriori commenti dalla direzione per comprendere le implicazioni future come la progettazione della Fase 3, l'interesse di partnership o le necessità di finanziamento.

Non sono stati allegati bilanci, dati sugli utili o dettagli transazionali. La società ha lasciato non selezionate tutte le caselle relative alla Regola 425, alla sollecitazione di deleghe e alle comunicazioni di offerte pubbliche di acquisto, indicando che il modulo 8-K si limita all’aggiornamento scientifico. Complessivamente, l’evento è potenzialmente rilevante, ma il suo impatto – positivo o negativo – resta incerto fino a quando i dati sottostanti non saranno esaminati.

El 30 de junio de 2025, INmune Bio, Inc. (NASDAQ: INMB) presentó un Formulario 8-K bajo el ítem 8.01 para informar un evento corporativo material. La compañía emitió un comunicado de prensa revelando los resultados preliminares de su ensayo de Fase 2 MINDFuL con XPro™ en pacientes con Alzheimer temprano. El 8-K en sí no incluye datos numéricos de eficacia o seguridad, pero incorpora el comunicado de prensa (Anexo 99.1) y una presentación corporativa actualizada (Anexo 99.2) por referencia, dirigiendo a los inversores a esos documentos para obtener detalles y la estrategia de desarrollo.

Esta divulgación marca un hito clínico clave para INmune Bio, ya que XPro es su principal activo en un mercado neurodegenerativo grande y de alto valor. Aunque la presentación confirma la finalización del ensayo y la disponibilidad de datos, la ausencia de resultados cuantitativos impide una evaluación inmediata del éxito clínico, la vía regulatoria o las perspectivas comerciales. Los inversores deberán revisar los anexos adjuntos o esperar comentarios adicionales de la dirección para evaluar las implicaciones futuras, como el diseño de la Fase 3, el interés de socios o las necesidades de financiamiento.

No se acompañaron estados financieros, cifras de ganancias ni detalles transaccionales. La compañía dejó sin marcar todas las casillas relacionadas con la Regla 425, la solicitud de poder y las comunicaciones de ofertas públicas de adquisición, indicando que el 8-K se limita a la actualización científica. En general, el evento es potencialmente material, pero su impacto —positivo o negativo— sigue siendo indeterminado hasta que se examinen los datos subyacentes.

2025년 6월 30일, INmune Bio, Inc. (NASDAQ: INMB)는 항목 8.01에 따라 중요한 기업 이벤트를 보고하기 위해 Form 8-K를 제출했습니다. 회사는 초기 알츠하이머 환자를 대상으로 한 XPro™의 2상 MINDFuL 시험의 주요 결과를 공개하는 보도자료를 발표했습니다. 8-K 자체에는 수치상의 효능 또는 안전성 데이터가 포함되어 있지 않으나, 보도자료(부록 99.1)와 업데이트된 기업 프레젠테이션(부록 99.2)을 참조로 포함하여 투자자들이 상세한 결과 및 개발 전략을 확인할 수 있도록 안내하고 있습니다.

이번 공시는 XPro가 크고 가치 있는 신경퇴행성 시장에서 INmune Bio의 주요 자산이기 때문에 중요한 임상 이정표를 의미합니다. 제출서류는 시험 완료 및 데이터 가용성을 확인하지만, 정량적 결과가 없어 즉각적인 임상 성공, 규제 경로 또는 상업적 전망 평가가 어렵습니다. 투자자들은 첨부 자료를 검토하거나 경영진의 추가 설명을 기다려 3상 설계, 파트너십 관심도, 자금 조달 요구사항 등 다음 단계에 대한 영향을 평가해야 합니다.

재무제표, 수익 수치 또는 거래 세부사항은 제출서류에 포함되지 않았습니다. 회사는 Rule 425, 위임장 청탁, 공개 매수 커뮤니케이션 관련 상자를 모두 체크하지 않아 8-K가 과학적 업데이트에 국한됨을 나타냅니다. 전반적으로 이번 이벤트는 잠재적으로 중요한 사항이지만, 근본 데이터가 검토되기 전까지 긍정적 또는 부정적 영향은 불확실합니다.

Le 30 juin 2025, INmune Bio, Inc. (NASDAQ : INMB) a déposé un formulaire 8-K sous l'item 8.01 pour signaler un événement d'entreprise important. La société a publié un communiqué de presse révélant les résultats préliminaires de son essai de phase 2 MINDFuL sur XPro™ chez des patients atteints d'Alzheimer précoce. Le 8-K lui-même ne contient pas de données numériques sur l'efficacité ou la sécurité, mais intègre par référence le communiqué de presse (Exhibit 99.1) et une présentation d'entreprise mise à jour (Exhibit 99.2), invitant les investisseurs à consulter ces documents pour les résultats détaillés et la stratégie de développement.

Cette divulgation marque une étape clinique cruciale pour INmune Bio car XPro est son principal actif sur un marché neurodégénératif vaste et à forte valeur. Bien que le dépôt confirme la fin de l'essai et la disponibilité des données, l'absence de résultats quantitatifs empêche une évaluation immédiate du succès clinique, de la voie réglementaire ou des perspectives commerciales. Les investisseurs devront examiner les annexes jointes ou attendre des commentaires supplémentaires de la direction pour évaluer les implications des prochaines étapes, telles que la conception de la phase 3, l'intérêt des partenaires ou les besoins de financement.

Aucun état financier, chiffre de résultats ou détail transactionnel n'accompagne le dépôt. La société a laissé toutes les cases relatives à la règle 425, à la sollicitation de procurations et aux communications d'offres publiques non cochées, indiquant que le 8-K se limite à la mise à jour scientifique. Dans l'ensemble, l'événement est potentiellement important, mais son impact – positif ou négatif – reste indéterminé jusqu'à ce que les données sous-jacentes soient examinées.

Am 30. Juni 2025 reichte INmune Bio, Inc. (NASDAQ: INMB) ein Formular 8-K unter Punkt 8.01 ein, um ein wesentliches Unternehmensereignis zu melden. Das Unternehmen veröffentlichte eine Pressemitteilung mit den vorläufigen Ergebnissen seiner Phase-2-MINDFuL-Studie zu XPro™ bei Patienten mit frühem Alzheimer. Das 8-K enthält keine numerischen Wirksamkeits- oder Sicherheitsdaten, verweist jedoch auf die Pressemitteilung (Anlage 99.1) und eine aktualisierte Unternehmenspräsentation (Anlage 99.2) und verweist Investoren auf diese Dokumente für detaillierte Ergebnisse und Entwicklungsstrategie.

Die Offenlegung stellt einen wichtigen klinischen Meilenstein für INmune Bio dar, da XPro sein führendes Produkt in einem großen, wertvollen neurodegenerativen Markt ist. Obwohl die Einreichung den Abschluss der Studie und die Verfügbarkeit der Daten bestätigt, verhindert das Fehlen quantitativer Ergebnisse eine sofortige Bewertung des klinischen Erfolgs, des regulatorischen Wegs oder der kommerziellen Aussichten. Investoren müssen die beigefügten Anlagen prüfen oder auf weitere Kommentare des Managements warten, um die nächsten Schritte wie die Planung der Phase 3, Partnerschaftsinteresse oder Finanzierungsbedarf zu bewerten.

Es wurden keine Finanzberichte, Gewinnzahlen oder Transaktionsdetails beigefügt. Das Unternehmen ließ alle Kästchen im Zusammenhang mit Regel 425, Stimmrechtsaufforderungen und Übernahmeangeboten ungeprüft, was darauf hinweist, dass das 8-K auf das wissenschaftliche Update beschränkt ist. Insgesamt ist das Ereignis potenziell wesentlich, aber seine Auswirkungen – positiv oder negativ – bleiben unbestimmt, bis die zugrunde liegenden Daten geprüft sind.

Positive
  • Release of Phase 2 topline results for lead Alzheimer’s candidate XPro indicates clinical progress and may catalyse strategic discussions.
Negative
  • None.

Insights

TL;DR: XPro Phase 2 read-out disclosed, but no numbers—material yet directionally unclear.

Clinical-stage biotech valuations hinge on data quality. Reaching a Phase 2 topline read-out for XPro is an important de-risking step, signalling trial execution competence and triggering possible engagement with regulators or partners. Alzheimer’s is a multibillion-dollar market with few disease-modifying options, so any credible signal could re-rate INMB. However, the 8-K withholds efficacy and safety metrics, leaving investors unable to judge effect size or statistical significance. Until investors examine Exhibits 99.1 and 99.2, sentiment is likely to stay cautious. I view the update as neutral pending data review.

TL;DR: Material disclosure with unknown outcome—risk profile unchanged for now.

Filing an 8-K signals management’s belief that the Phase 2 results are material. Yet withholding specifics keeps asymmetric-information risk elevated; insiders already know whether the data are strong or weak. Absent publicly posted numbers, volatility may spike once investors locate the exhibits or third-party commentary emerges. From a governance perspective, the company complied with prompt disclosure rules, reducing regulatory risk. Financial risk-return dynamics, however, remain unchanged until data clarity arrives.

Il 30 giugno 2025, INmune Bio, Inc. (NASDAQ: INMB) ha presentato un modulo 8-K ai sensi dell'Elemento 8.01 per comunicare un evento aziendale rilevante. La società ha diffuso un comunicato stampa che annuncia i risultati preliminari della Fase 2 dello studio MINDFuL su XPro™ in pazienti con Alzheimer precoce. Il modulo 8-K non include dati numerici sull'efficacia o sicurezza, ma integra il comunicato stampa (Allegato 99.1) e una presentazione aziendale aggiornata (Allegato 99.2) tramite riferimento, indirizzando gli investitori a tali documenti per approfondimenti e strategie di sviluppo.

Questa divulgazione rappresenta una tappa clinica fondamentale per INmune Bio, poiché XPro è il suo principale prodotto in un mercato neurodegenerativo ampio e di grande valore. Sebbene la comunicazione confermi il completamento dello studio e la disponibilità dei dati, l'assenza di risultati quantitativi impedisce una valutazione immediata del successo clinico, del percorso regolatorio o delle prospettive commerciali. Gli investitori dovranno consultare gli allegati o attendere ulteriori commenti dalla direzione per comprendere le implicazioni future come la progettazione della Fase 3, l'interesse di partnership o le necessità di finanziamento.

Non sono stati allegati bilanci, dati sugli utili o dettagli transazionali. La società ha lasciato non selezionate tutte le caselle relative alla Regola 425, alla sollecitazione di deleghe e alle comunicazioni di offerte pubbliche di acquisto, indicando che il modulo 8-K si limita all’aggiornamento scientifico. Complessivamente, l’evento è potenzialmente rilevante, ma il suo impatto – positivo o negativo – resta incerto fino a quando i dati sottostanti non saranno esaminati.

El 30 de junio de 2025, INmune Bio, Inc. (NASDAQ: INMB) presentó un Formulario 8-K bajo el ítem 8.01 para informar un evento corporativo material. La compañía emitió un comunicado de prensa revelando los resultados preliminares de su ensayo de Fase 2 MINDFuL con XPro™ en pacientes con Alzheimer temprano. El 8-K en sí no incluye datos numéricos de eficacia o seguridad, pero incorpora el comunicado de prensa (Anexo 99.1) y una presentación corporativa actualizada (Anexo 99.2) por referencia, dirigiendo a los inversores a esos documentos para obtener detalles y la estrategia de desarrollo.

Esta divulgación marca un hito clínico clave para INmune Bio, ya que XPro es su principal activo en un mercado neurodegenerativo grande y de alto valor. Aunque la presentación confirma la finalización del ensayo y la disponibilidad de datos, la ausencia de resultados cuantitativos impide una evaluación inmediata del éxito clínico, la vía regulatoria o las perspectivas comerciales. Los inversores deberán revisar los anexos adjuntos o esperar comentarios adicionales de la dirección para evaluar las implicaciones futuras, como el diseño de la Fase 3, el interés de socios o las necesidades de financiamiento.

No se acompañaron estados financieros, cifras de ganancias ni detalles transaccionales. La compañía dejó sin marcar todas las casillas relacionadas con la Regla 425, la solicitud de poder y las comunicaciones de ofertas públicas de adquisición, indicando que el 8-K se limita a la actualización científica. En general, el evento es potencialmente material, pero su impacto —positivo o negativo— sigue siendo indeterminado hasta que se examinen los datos subyacentes.

2025년 6월 30일, INmune Bio, Inc. (NASDAQ: INMB)는 항목 8.01에 따라 중요한 기업 이벤트를 보고하기 위해 Form 8-K를 제출했습니다. 회사는 초기 알츠하이머 환자를 대상으로 한 XPro™의 2상 MINDFuL 시험의 주요 결과를 공개하는 보도자료를 발표했습니다. 8-K 자체에는 수치상의 효능 또는 안전성 데이터가 포함되어 있지 않으나, 보도자료(부록 99.1)와 업데이트된 기업 프레젠테이션(부록 99.2)을 참조로 포함하여 투자자들이 상세한 결과 및 개발 전략을 확인할 수 있도록 안내하고 있습니다.

이번 공시는 XPro가 크고 가치 있는 신경퇴행성 시장에서 INmune Bio의 주요 자산이기 때문에 중요한 임상 이정표를 의미합니다. 제출서류는 시험 완료 및 데이터 가용성을 확인하지만, 정량적 결과가 없어 즉각적인 임상 성공, 규제 경로 또는 상업적 전망 평가가 어렵습니다. 투자자들은 첨부 자료를 검토하거나 경영진의 추가 설명을 기다려 3상 설계, 파트너십 관심도, 자금 조달 요구사항 등 다음 단계에 대한 영향을 평가해야 합니다.

재무제표, 수익 수치 또는 거래 세부사항은 제출서류에 포함되지 않았습니다. 회사는 Rule 425, 위임장 청탁, 공개 매수 커뮤니케이션 관련 상자를 모두 체크하지 않아 8-K가 과학적 업데이트에 국한됨을 나타냅니다. 전반적으로 이번 이벤트는 잠재적으로 중요한 사항이지만, 근본 데이터가 검토되기 전까지 긍정적 또는 부정적 영향은 불확실합니다.

Le 30 juin 2025, INmune Bio, Inc. (NASDAQ : INMB) a déposé un formulaire 8-K sous l'item 8.01 pour signaler un événement d'entreprise important. La société a publié un communiqué de presse révélant les résultats préliminaires de son essai de phase 2 MINDFuL sur XPro™ chez des patients atteints d'Alzheimer précoce. Le 8-K lui-même ne contient pas de données numériques sur l'efficacité ou la sécurité, mais intègre par référence le communiqué de presse (Exhibit 99.1) et une présentation d'entreprise mise à jour (Exhibit 99.2), invitant les investisseurs à consulter ces documents pour les résultats détaillés et la stratégie de développement.

Cette divulgation marque une étape clinique cruciale pour INmune Bio car XPro est son principal actif sur un marché neurodégénératif vaste et à forte valeur. Bien que le dépôt confirme la fin de l'essai et la disponibilité des données, l'absence de résultats quantitatifs empêche une évaluation immédiate du succès clinique, de la voie réglementaire ou des perspectives commerciales. Les investisseurs devront examiner les annexes jointes ou attendre des commentaires supplémentaires de la direction pour évaluer les implications des prochaines étapes, telles que la conception de la phase 3, l'intérêt des partenaires ou les besoins de financement.

Aucun état financier, chiffre de résultats ou détail transactionnel n'accompagne le dépôt. La société a laissé toutes les cases relatives à la règle 425, à la sollicitation de procurations et aux communications d'offres publiques non cochées, indiquant que le 8-K se limite à la mise à jour scientifique. Dans l'ensemble, l'événement est potentiellement important, mais son impact – positif ou négatif – reste indéterminé jusqu'à ce que les données sous-jacentes soient examinées.

Am 30. Juni 2025 reichte INmune Bio, Inc. (NASDAQ: INMB) ein Formular 8-K unter Punkt 8.01 ein, um ein wesentliches Unternehmensereignis zu melden. Das Unternehmen veröffentlichte eine Pressemitteilung mit den vorläufigen Ergebnissen seiner Phase-2-MINDFuL-Studie zu XPro™ bei Patienten mit frühem Alzheimer. Das 8-K enthält keine numerischen Wirksamkeits- oder Sicherheitsdaten, verweist jedoch auf die Pressemitteilung (Anlage 99.1) und eine aktualisierte Unternehmenspräsentation (Anlage 99.2) und verweist Investoren auf diese Dokumente für detaillierte Ergebnisse und Entwicklungsstrategie.

Die Offenlegung stellt einen wichtigen klinischen Meilenstein für INmune Bio dar, da XPro sein führendes Produkt in einem großen, wertvollen neurodegenerativen Markt ist. Obwohl die Einreichung den Abschluss der Studie und die Verfügbarkeit der Daten bestätigt, verhindert das Fehlen quantitativer Ergebnisse eine sofortige Bewertung des klinischen Erfolgs, des regulatorischen Wegs oder der kommerziellen Aussichten. Investoren müssen die beigefügten Anlagen prüfen oder auf weitere Kommentare des Managements warten, um die nächsten Schritte wie die Planung der Phase 3, Partnerschaftsinteresse oder Finanzierungsbedarf zu bewerten.

Es wurden keine Finanzberichte, Gewinnzahlen oder Transaktionsdetails beigefügt. Das Unternehmen ließ alle Kästchen im Zusammenhang mit Regel 425, Stimmrechtsaufforderungen und Übernahmeangeboten ungeprüft, was darauf hinweist, dass das 8-K auf das wissenschaftliche Update beschränkt ist. Insgesamt ist das Ereignis potenziell wesentlich, aber seine Auswirkungen – positiv oder negativ – bleiben unbestimmt, bis die zugrunde liegenden Daten geprüft sind.

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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): June 30, 2025 (June 28, 2025)

 

AIMFINITY INVESTMENT CORP. I

(Exact name of registrant as specified in its charter)

 

Cayman Islands   001-41361   N/A
(State or other jurisdiction   (Commission File Number)   (IRS Employer
of incorporation)       Identification Number)

 

221 W 9th St, PMB 235
Wilmington
, Delaware 19801

(Address of principal executive offices)

 

(425) 365-2933

(Registrant’s telephone number, including area code)

 

  

(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   Name of each exchange on
which registered
Units, consisting of one New Unit and one Class 1 redeemable warrant, each exercisable for one Class A ordinary share at an exercise price of $11.50   AIMUF   OTC Market Group, Inc.
New Units, consisting of one Class A ordinary share and one-half of one Class 2 redeemable warrant, each full exercisable for one Class A ordinary share at an exercise price of $11.50   AIMTF   OTC Market Group, Inc.
Class 1 redeemable warrants, each exercisable for one Class A ordinary share at an exercise price of $11.50   AIMWF   OTC Market Group, Inc.

 

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 2.03 Creation of a Direct Financial Obligation or an Obligation under an Off-Balance Sheet Arrangement of a Registrant

 

As previously disclosed by Aimfinity Investment Corp. I (“AIMA” or the “Company”) in its Current Report on Form 8-K filed on October 16, 2023, on October 13, 2023, the Company entered into that certain Agreement and Plan of Merger (as may be amended, supplemented or otherwise modified from time to time, the “Merger Agreement”), with Docter Inc., a Delaware corporation (“Docter”), Aimfinity Investment Merger Sub I, a Cayman Islands exempted company and wholly-owned subsidiary of AIMA (“Purchaser”), and Aimfinity Investment Merger Sub II, Inc., a Delaware corporation and wholly-owned subsidiary of Purchaser (“Merger Sub”), pursuant to which AIMA will complete a business combination (the “Business Combination”) with Docter that involves a reincorporation merger and an acquisition merger. The Purchaser shall survive the Business Combination and be referred to as “PubCo” after the Business Combination.

 

On January 9, 2025, the Company held an extraordinary general meeting, where the shareholders of the Company approved to amend the Company’s amended and restated memorandum and articles of associations (the “Charter”) to allow the Company until January 28, 2025 to consummate an initial business combination and may elect to extend the period to consummate an initial business combination up to nine times, each by an additional one-month period (each, a “Monthly Extension”), for a total of up to nine months to October 28, 2025, by depositing into the Company’s trust account (the “Trust Account”) an amount equal to $0.05 for each public share for each one-month extension.

 

On June 28, 2025, the Company issued an unsecured promissory note of $55,823.8 (the “Note”) to I-Fa Chang, a member and manager of Aimfinity Investment LLC, the sponsor of the Company (the “Sponsor”), as the Sponsor’s designee, to evidence the payments made for $55,823.8 (the “New Monthly Extension Payment”) to be deposited into the Trust Account for the public shareholders, which enables the Company to extend the period of time it has to consummate the Business Combination by one month from June 28, 2025 to July 28, 2025 (the “New Extension”). The New Extension is the sixth of nine possible Monthly Extensions permitted under the Charter.

 

Pursuant to the Note, and a certain exchange agreement, dated April 8, 2025, by and among the Company, Mr. Chang and certain other parties to the Merger Agreement, upon the closing of the Business Combination by and between the Company and Docter, the balance of the Note, unless repaid in part or in full, will automatically be exchanged for such number of PubCo ordinary shares at a conversion price of $10.00 per share. The Note was issued pursuant to the exemption from registration under Section 4(a)(2) of the Securities Act of 1933, as amended (the “Securities Act”).

 

A copy of the Note is filed as Exhibit 10.2 to this Current Report on Form 8-K and is incorporated herein by reference. The disclosures set forth in this Item 2.03 are intended to be summaries only and are qualified in their entirety by reference to the Note.

 

Item 3.02 Unregistered Sales of Equity Securities.

 

The information disclosed under Items 1.01 and 2.03 of this Current Report on Form 8-K is incorporated by reference into this Item 3.02 to the extent required herein.

 

Item 7.01 Regulation FD Disclosure.

 

On June 30, 2025, the Company issued a press release (the “Press Release”) announcing the New Extension. A copy of the Press Release is furnished as Exhibit 99.1 hereto. The information in this Item 7.01 and Exhibit 99.1 furnished hereto shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act or the Exchange Act, except as expressly set forth by specific reference in such filing.

 

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IMPORTANT NOTICES

 

As disclosed previously on the Current Report on Form 8-K filed with the Securities and Exchange Commission (the “SEC”) on October 16, 2023, on October 13, 2023, AIMA entered into that certain Merger Agreement, with Docter, Purchaser, and Merger Sub, pursuant to which AIMA will complete a business combination with Docter that involves a reincorporation merger and an acquisition merger.

 

This Current Report on Form 8-K contains certain “forward-looking statements” within the meaning of the Securities Act and the Exchange Act. Statements that are not historical facts, including statements about the proposed transactions described above, and the parties’ perspectives and expectations, are forward-looking statements. Such statements include, but are not limited to, statements regarding the proposed transactions, including the anticipated initial enterprise value and post-closing equity value, the benefits of the proposed transaction, integration plans, expected synergies and revenue opportunities, anticipated future financial and operating performance and results, including estimates for growth, the expected management and governance of the combined company, and the expected timing of the proposed transactions. The words “expect,” “believe,” “estimate,” “intend,” “plan” and similar expressions indicate forward-looking statements. These forward-looking statements are not guarantees of future performance and are subject to various risks and uncertainties, assumptions (including assumptions about general economic, market, industry and operational factors), known or unknown, which could cause the actual results to vary materially from those indicated or anticipated.

 

Such risks and uncertainties include, but are not limited to: (i) risks related to the expected timing and likelihood of completion of the proposed business combination, including the risk that the transaction may not close due to one or more closing conditions to the transaction not being satisfied or waived, such as regulatory approvals not being obtained, on a timely basis or otherwise, or that a governmental entity prohibited, delayed or refused to grant approval for the consummation of the transaction or required certain conditions, limitations or restrictions in connection with such approvals; (ii) risks related to the ability of AIMA and Docter to successfully integrate the businesses; (iii) the occurrence of any event, change or other circumstances that could give rise to the termination of the applicable transaction agreements; (iv) the risk that there may be a material adverse change with respect to the financial position, performance, operations or prospects of Docter or AIMA; (v) risks related to disruption of management time from ongoing business operations due to the proposed transaction; (vi) the risk that any announcements relating to the proposed transaction could have adverse effects on the market price of AIMA’s securities; (vii) the risk that the proposed transaction and its announcement could have an adverse effect on the ability of Docter to retain customers and retain and hire key personnel and maintain relationships with their suppliers and customers and on their operating results and businesses generally; (viii) risks relating to the health monitoring device industry, including but not limited to governmental regulatory and enforcement changes, market competitions, competitive product and pricing activity; and (ix) risks relating to the combined company’s ability to enhance its products and services, execute its business strategy, expand its customer base and maintain stable relationship with its business partners. A further list and description of risks and uncertainties can be found in the prospectus filed with the SEC on April 26, 2022 relating to AIMA’s initial public offering (File No. 333-263874), the annual report of AIMA on Form 10-K for the fiscal year ended on December 31, 2024, filed with the SEC on April 15, 2025 (the “Annual Report”), and in the final prospectus/proxy statement filed with the SEC on March 6, 2025 relating to the proposed transactions (File No. 333-284658) (the “Final Prospectus”), and other documents that the parties may file or furnish with the SEC, which you are encouraged to read. Should one or more of these risks or uncertainties materialize, or should underlying assumptions prove incorrect, actual results may vary materially from those indicated or anticipated by such forward-looking statements. Accordingly, you are cautioned not to place undue reliance on these forward-looking statements. Forward-looking statements relate only to the date they were made, and AIMA, Docter and their subsidiaries or affiliates undertake no obligation to update forward-looking statements to reflect events or circumstances after the date they were made except as required by law or applicable regulation.

 

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Additional Information and Where to Find It

 

In connection with the proposed transactions described herein, Purchaser filed the Final Prospectus with the SEC on March 6, 2025 and AIMA held an extraordinary general meeting on March 27, 2025 where the Business Combination was approved by holders of a requisite number of ordinary shares of AIMA.. Shareholders will also be able to obtain a copy of the Final Prospectus without charge from AIMA. The Final Prospectus may also be obtained without charge at the SEC’s website at www.sec.gov. INVESTORS AND SECURITY HOLDERS OF AIMA ARE URGED TO READ THESE MATERIALS (INCLUDING ANY AMENDMENTS OR SUPPLEMENTS THERETO) AND ANY OTHER RELEVANT DOCUMENTS IN CONNECTION WITH THE PROPOSED TRANSACTIONS THAT AIMA WILL FILE WITH THE SEC WHEN THEY BECOME AVAILABLE BECAUSE THEY WILL CONTAIN IMPORTANT INFORMATION ABOUT AIMA, THE COMPANY AND THE PROPOSED TRANSACTIONS.

 

Participants in Solicitation

 

AIMA, Docter, 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 AIMA’s shareholders in connection with the proposed transactions described herein. Information regarding the persons who may, under SEC rules, be deemed participants in the solicitation of AIMA’s shareholders in connection with the proposed business combination is set forth in the Final Prospectus.

 

No Offer or Solicitation

 

This Current Report on Form 8-K is not a proxy statement or solicitation of a proxy, consent or authorization with respect to any securities or in respect of the proposed transactions described herein and shall not constitute an offer to sell or a solicitation of an offer to buy the securities of AIMA or Docter, nor shall there be any sale of any such securities in any state or jurisdiction in which such offer, solicitation, or sale would be unlawful prior to registration or qualification under the securities laws of such state or jurisdiction. No offering of securities shall be made except by means of a prospectus meeting the requirements of Section 10 of the Securities Act or an exemption therefrom. 

 

Item 9.01 Financial Statements and Exhibits.

 

(d) Exhibits.

 

Exhibit No.   Description
10.1   Promissory Note, dated June 28, 2025, issued by the Company to I-Fa Chang.
99.1   Press Release
104   Cover Page Interactive Data File (embedded within the Inline XBRL document).

 

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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.

 

  Aimfinity Investment Corp. I
   
Date: June 30, 2025 By: /s/ I-Fa Chang
  Name:  I-Fa Chang
  Title: Chief Executive Officer

 

 

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FAQ

What did INMB announce in its June 30 2025 Form 8-K?

The company disclosed topline Phase 2 MINDFuL trial results for XPro™ in early Alzheimer’s disease and provided an updated corporate presentation.

Where can investors find detailed data on the XPro Phase 2 trial?

Detailed information is in Exhibit 99.1 (press release) and Exhibit 99.2 (corporate presentation) attached to the 8-K.

Does the 8-K include any financial statements or earnings figures?

No. Item 8.01 addresses other events only; no financial statements or earnings data are provided.

Which item of the 8-K covers the announcement?

The event is reported under Item 8.01 – Other Events.

What exhibits were filed with the Form 8-K?

Exhibit 99.1: Press Release dated June 30 2025; Exhibit 99.2: Corporate Presentation; Exhibit 104: Cover Page Interactive Data File.
Aimfinity Investment I Corp

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