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[8-K] Aptevo Therapeutics Inc Reports Material Event

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

Aptevo Therapeutics Inc. (NASDAQ: APVO) filed an 8-K to disclose a capital raise and several portfolio updates. On 18 June 2025 the Company signed a Securities Purchase Agreement with institutional investors for a registered direct offering (the “Offering”) that closed on 20 June 2025. The structure consisted of (i) 2,105,000 shares of common stock and (ii) pre-funded warrants for up to 360,000 shares, each sold together with five five-year common warrants (exercise price $3.25). The unit price was $3.25 for stock or $3.249 for a pre-funded warrant, reflecting the $0.0001 exercise price on the pre-funded component.

The common warrants cannot be exercised until stockholder approval is obtained under Nasdaq Capital Market rules; if approval is not obtained, the warrants become non-exercisable and have no value. The exercise price is subject to customary anti-dilution adjustments but will not reset below $0.65. Pre-funded warrants are immediately exercisable at $0.001 per share and remain outstanding until fully exercised.

The Company received net proceeds of approximately $7.45 million after deducting estimated offering expenses and a 7.0 % placement fee paid to Roth Capital Partners, LLC, which served as exclusive placement agent under a separate Placement Agency Agreement. Aptevo has agreed (1) not to issue additional equity until the earlier of stockholder approval or 60 days after closing, and (2) not to enter variable-price security agreements for three months, subject to usual exceptions.

Use of proceeds: working capital, funding of clinical programs and general corporate purposes, including continued development of its product candidates.

Pipeline communications: Concurrent press releases announced (i) data from the ongoing Phase 1b/2 RAINIER trial of CD123 × CD3 bispecific mipletamig in AML, and (ii) the addition of pre-clinical candidate APVO455, expanding the Company’s CD3-directed portfolio for hematologic and solid tumors. No efficacy or safety metrics were included in the filing.

Key takeaways for investors

  • Approximately $7.45 million of fresh capital extends runway and supports clinical milestones.
  • Unit structure with five leverage-creating common warrants introduces a substantial potential dilution overhang (up to 12.3 million shares) if stockholder approval is obtained and warrants are exercised.
  • Failure to secure approval would render warrants valueless, potentially disappointing investors who participated for warrant upside but limiting future dilution for existing shareholders.
  • Lock-up provisions are relatively short, limiting near-term additional issuance but not providing long-term protection.
  • Pipeline momentum continues with new candidate APVO455 and ongoing mipletamig study, signaling R&D progress, though concrete clinical data are not yet disclosed.

Aptevo Therapeutics Inc. (NASDAQ: APVO) ha presentato un modulo 8-K per comunicare un aumento di capitale e aggiornamenti sul portafoglio prodotti. Il 18 giugno 2025 la Società ha firmato un Accordo di Acquisto di Titoli con investitori istituzionali per un'offerta diretta registrata (l’“Offerta”) che si è conclusa il 20 giugno 2025. La struttura prevedeva (i) 2.105.000 azioni ordinarie e (ii) warrant pre-finanziati per un massimo di 360.000 azioni, ciascuno venduto insieme a cinque warrant ordinari quinquennali (prezzo di esercizio $3,25). Il prezzo unitario era di $3,25 per azione o $3,249 per warrant pre-finanziato, riflettendo il prezzo di esercizio di $0,0001 sulla componente pre-finanziata.

I warrant ordinari non possono essere esercitati fino a quando non viene ottenuta l’approvazione degli azionisti secondo le regole del Nasdaq Capital Market; in caso contrario, i warrant diventano inesercitabili e privi di valore. Il prezzo di esercizio è soggetto a consueti aggiustamenti anti-diluizione ma non potrà scendere sotto $0,65. I warrant pre-finanziati sono esercitabili immediatamente a $0,001 per azione e rimangono validi fino al completo esercizio.

La Società ha ricevuto proventi netti di circa 7,45 milioni di dollari dopo aver dedotto le spese stimate dell’offerta e una commissione di collocamento del 7,0 % pagata a Roth Capital Partners, LLC, che ha agito come agente di collocamento esclusivo secondo un accordo separato. Aptevo si è impegnata (1) a non emettere ulteriori azioni fino al primo tra l’approvazione degli azionisti o 60 giorni dopo la chiusura, e (2) a non stipulare accordi su titoli a prezzo variabile per tre mesi, salvo eccezioni consuete.

Utilizzo dei proventi: capitale circolante, finanziamento di programmi clinici e scopi aziendali generali, inclusa la prosecuzione dello sviluppo dei candidati farmaceutici.

Aggiornamenti sul portafoglio: comunicati stampa paralleli hanno annunciato (i) dati dallo studio in corso di Fase 1b/2 RAINIER sul bispecifico CD123 × CD3 mipletamig in leucemia mieloide acuta (AML), e (ii) l’aggiunta del candidato pre-clinico APVO455, ampliando il portafoglio CD3 diretto a tumori ematologici e solidi. Nel deposito non sono stati inclusi dati di efficacia o sicurezza.

Punti chiave per gli investitori

  • Circa 7,45 milioni di dollari di nuovo capitale estendono la liquidità e supportano traguardi clinici.
  • La struttura dell’unità con cinque warrant ordinari a leva introduce un potenziale significativo rischio di diluizione (fino a 12,3 milioni di azioni) se si ottiene l’approvazione degli azionisti e i warrant vengono esercitati.
  • La mancata approvazione renderebbe i warrant privi di valore, deludendo gli investitori interessati al potenziale dei warrant ma limitando la diluizione futura per gli azionisti esistenti.
  • Le clausole di lock-up sono relativamente brevi, limitando ulteriori emissioni a breve termine ma non garantendo una protezione a lungo termine.
  • Il portafoglio continua a crescere con il nuovo candidato APVO455 e lo studio in corso su mipletamig, segnalando progressi nella R&S, anche se dati clinici concreti non sono ancora stati resi noti.

Aptevo Therapeutics Inc. (NASDAQ: APVO) presentó un formulario 8-K para revelar una ampliación de capital y varias actualizaciones de su cartera. El 18 de junio de 2025, la Compañía firmó un Acuerdo de Compra de Valores con inversores institucionales para una oferta directa registrada (la “Oferta”) que se cerró el 20 de junio de 2025. La estructura consistió en (i) 2.105.000 acciones comunes y (ii) warrants prefinanciados para hasta 360.000 acciones, cada uno vendido junto con cinco warrants comunes a cinco años (precio de ejercicio $3,25). El precio unitario fue $3,25 por acción o $3,249 por warrant prefinanciado, reflejando el precio de ejercicio de $0,0001 en la parte prefinanciada.

Los warrants comunes no pueden ejercerse hasta obtener la aprobación de los accionistas según las reglas del Nasdaq Capital Market; si no se obtiene dicha aprobación, los warrants se vuelven no ejercitables y sin valor. El precio de ejercicio está sujeto a ajustes anti-dilución habituales, pero no podrá bajar de $0,65. Los warrants prefinanciados son ejercitables inmediatamente a $0,001 por acción y permanecen vigentes hasta ser totalmente ejercidos.

La Compañía recibió ingresos netos de aproximadamente $7,45 millones después de deducir los gastos estimados de la oferta y una comisión de colocación del 7,0 % pagada a Roth Capital Partners, LLC, que actuó como agente exclusivo de colocación bajo un Acuerdo de Agencia de Colocación separado. Aptevo se comprometió (1) a no emitir acciones adicionales hasta la aprobación de los accionistas o 60 días después del cierre, lo que ocurra primero, y (2) a no celebrar acuerdos de valores con precio variable durante tres meses, sujeto a excepciones habituales.

Uso de los ingresos: capital de trabajo, financiación de programas clínicos y propósitos corporativos generales, incluyendo el desarrollo continuo de sus candidatos a productos.

Comunicaciones sobre la cartera: Comunicados de prensa simultáneos anunciaron (i) datos del ensayo en curso de Fase 1b/2 RAINIER del bispecífico CD123 × CD3 mipletamig en leucemia mieloide aguda (LMA), y (ii) la incorporación del candidato preclínico APVO455, ampliando la cartera dirigida a CD3 para tumores hematológicos y sólidos. No se incluyeron métricas de eficacia o seguridad en la presentación.

Puntos clave para inversores

  • Aproximadamente $7,45 millones en capital fresco extienden la pista financiera y apoyan hitos clínicos.
  • La estructura de la unidad con cinco warrants comunes apalancados introduce un potencial importante riesgo de dilución (hasta 12,3 millones de acciones) si se obtiene la aprobación de los accionistas y se ejercen los warrants.
  • La falta de aprobación haría que los warrants no tengan valor, lo que podría decepcionar a los inversores que apostaron por el potencial de los warrants, pero limitaría la dilución futura para los accionistas existentes.
  • Las disposiciones de bloqueo son relativamente cortas, limitando emisiones adicionales a corto plazo pero sin ofrecer protección a largo plazo.
  • El impulso de la cartera continúa con el nuevo candidato APVO455 y el estudio en curso de mipletamig, señalando progreso en I+D, aunque aún no se han divulgado datos clínicos concretos.

Aptevo Therapeutics Inc. (NASDAQ: APVO)는 자본 조달 및 포트폴리오 업데이트를 공개하기 위해 8-K 보고서를 제출했습니다. 2025년 6월 18일 회사는 기관 투자자들과 등록 직접 공모(“공모”)를 위한 증권 매매 계약을 체결했으며, 해당 공모는 2025년 6월 20일에 마감되었습니다. 구조는 (i) 보통주 2,105,000주와 (ii) 최대 360,000주에 대한 선행 자금 납입 워런트로 구성되었으며, 각각 5년 만기 보통주 워런트 5개(행사가 $3.25)와 함께 판매되었습니다. 단가(stock)는 주식 $3.25 또는 선행 자금 납입 워런트 $3.249로, 선행 자금 부분의 행사가 $0.0001을 반영합니다.

보통주 워런트는 Nasdaq Capital Market 규정에 따라 주주 승인이 있을 때까지 행사할 수 없으며, 승인이 없으면 워런트는 행사 불가능하며 가치가 없습니다. 행사가격은 통상적인 희석 방지 조정 대상이나 $0.65 아래로는 조정되지 않습니다. 선행 자금 납입 워런트는 주당 $0.001에 즉시 행사 가능하며 전부 행사될 때까지 유효합니다.

회사는 추정 공모 비용과 7.0% 배치 수수료를 Roth Capital Partners, LLC에 지급한 후 약 745만 달러의 순수익을 받았습니다. Roth Capital Partners는 별도의 배치 대행 계약에 따라 독점 배치 대행사로 활동했습니다. Aptevo는 (1) 주주 승인 또는 마감 후 60일 중 빠른 시점까지 추가 주식 발행을 하지 않으며, (2) 일반적인 예외를 제외하고 3개월간 변동 가격 증권 계약을 체결하지 않기로 합의했습니다.

수익금 사용처: 운전자본, 임상 프로그램 자금 조달 및 일반 기업 목적, 제품 후보군 개발 지속 포함.

파이프라인 소식: 동시 보도자료를 통해 (i) AML(급성 골수성 백혈병) 대상 CD123 × CD3 이중특이적 mipletamig의 진행 중인 1b/2상 RAINIER 시험 데이터, (ii) 혈액암 및 고형암 대상 CD3 지향 포트폴리오 확장을 위한 전임상 후보 APVO455 추가를 발표했습니다. 제출 자료에는 효능 또는 안전성 지표는 포함되지 않았습니다.

투자자를 위한 주요 요점

  • 약 745만 달러의 신규 자본이 자금 여력을 연장하고 임상 마일스톤을 지원합니다.
  • 5개의 레버리지 보통주 워런트가 포함된 단위 구조는 주주 승인 후 워런트 행사 시 최대 1,230만 주까지 상당한 희석 가능성을 내포합니다.
  • 승인 실패 시 워런트는 무가치해져 워런트 상승 잠재력을 기대한 투자자에게는 실망을 줄 수 있으나 기존 주주에겐 미래 희석을 제한합니다.
  • 락업 조항은 비교적 짧아 단기 추가 발행을 제한하지만 장기 보호는 제공하지 않습니다.
  • 신규 후보 APVO455와 진행 중인 mipletamig 연구로 파이프라인 모멘텀이 지속되고 있어 연구개발 진전을 시사하나 구체적인 임상 데이터는 아직 공개되지 않았습니다.

Aptevo Therapeutics Inc. (NASDAQ : APVO) a déposé un formulaire 8-K pour annoncer une levée de fonds et plusieurs mises à jour de son portefeuille. Le 18 juin 2025, la Société a signé un accord d'achat de titres avec des investisseurs institutionnels pour une offre directe enregistrée (l’« Offre ») qui s’est clôturée le 20 juin 2025. La structure comprenait (i) 2 105 000 actions ordinaires et (ii) des bons de souscription préfinancés pour jusqu’à 360 000 actions, chacun vendu avec cinq bons de souscription ordinaires d’une durée de cinq ans (prix d’exercice de 3,25 $). Le prix unitaire était de 3,25 $ pour l’action ou 3,249 $ pour le bon préfinancé, reflétant le prix d’exercice de 0,0001 $ sur la composante préfinancée.

Les bons ordinaires ne peuvent être exercés qu’après approbation des actionnaires conformément aux règles du Nasdaq Capital Market ; sans cette approbation, les bons deviennent inexerçables et sans valeur. Le prix d’exercice est soumis à des ajustements anti-dilution habituels mais ne pourra pas être inférieur à 0,65 $. Les bons préfinancés sont immédiatement exerçables à 0,001 $ par action et restent en circulation jusqu’à leur exercice complet.

La Société a reçu environ 7,45 millions de dollars nets après déduction des frais estimés de l’offre et d’une commission de placement de 7,0 % versée à Roth Capital Partners, LLC, qui a agi en tant qu’agent de placement exclusif dans le cadre d’un accord distinct. Aptevo s’est engagée (1) à ne pas émettre d’actions supplémentaires avant l’approbation des actionnaires ou 60 jours après la clôture, selon la première éventualité, et (2) à ne pas conclure d’accords sur des titres à prix variable pendant trois mois, sous réserve des exceptions habituelles.

Utilisation des fonds : fonds de roulement, financement des programmes cliniques et objectifs généraux de l’entreprise, y compris le développement continu de ses candidats produits.

Communications sur le portefeuille : Des communiqués de presse simultanés ont annoncé (i) des données de l’essai de phase 1b/2 RAINIER en cours sur le bispécifique CD123 × CD3 mipletamig dans la leucémie myéloïde aiguë (LMA), et (ii) l’ajout du candidat préclinique APVO455, élargissant le portefeuille dirigé contre CD3 pour les tumeurs hématologiques et solides. Aucun indicateur d’efficacité ou de sécurité n’a été inclus dans le dépôt.

Points clés pour les investisseurs

  • Environ 7,45 millions de dollars de capital frais prolongent la trésorerie et soutiennent les jalons cliniques.
  • La structure de l’unité avec cinq bons ordinaires à effet de levier introduit un risque important de dilution potentielle (jusqu’à 12,3 millions d’actions) si l’approbation des actionnaires est obtenue et que les bons sont exercés.
  • L’absence d’approbation rendrait les bons sans valeur, ce qui pourrait décevoir les investisseurs ayant parié sur le potentiel des bons mais limiterait la dilution future pour les actionnaires existants.
  • Les clauses de lock-up sont relativement courtes, limitant les émissions supplémentaires à court terme mais sans offrir de protection à long terme.
  • Le portefeuille progresse avec le nouveau candidat APVO455 et l’étude en cours sur mipletamig, indiquant des avancées en R&D, bien que des données cliniques concrètes ne soient pas encore divulguées.

Aptevo Therapeutics Inc. (NASDAQ: APVO) reichte ein 8-K ein, um eine Kapitalerhöhung und mehrere Portfolio-Updates bekannt zu geben. Am 18. Juni 2025 unterzeichnete das Unternehmen eine Wertpapierkaufvereinbarung mit institutionellen Investoren für ein registriertes Direktangebot (das „Angebot“), das am 20. Juni 2025 abgeschlossen wurde. Die Struktur bestand aus (i) 2.105.000 Stammaktien und (ii) vorfinanzierten Optionsscheinen für bis zu 360.000 Aktien, die jeweils zusammen mit fünf fünfjährigen Stammoptionsscheinen (Ausübungspreis 3,25 $) verkauft wurden. Der Stückpreis betrug 3,25 $ für Aktien bzw. 3,249 $ für einen vorfinanzierten Optionsschein, was den Ausübungspreis von 0,0001 $ für die vorfinanzierte Komponente widerspiegelt.

Die Stammoptionsscheine können erst ausgeübt werden, wenn die Zustimmung der Aktionäre gemäß den Regeln des Nasdaq Capital Market vorliegt; wird diese nicht erteilt, werden die Optionsscheine unverwertbar und wertlos. Der Ausübungspreis unterliegt üblichen Verwässerungsschutzanpassungen, wird jedoch nicht unter 0,65 $ zurückgesetzt. Vorfinanzierte Optionsscheine sind sofort zum Preis von 0,001 $ pro Aktie ausübbar und bleiben bis zur vollständigen Ausübung gültig.

Das Unternehmen erhielt Nettoerlöse von ca. 7,45 Millionen US-Dollar nach Abzug der geschätzten Angebotskosten und einer 7,0 %igen Platzierungsgebühr, die an Roth Capital Partners, LLC gezahlt wurde, die als exklusiver Platzierungsagent im Rahmen einer separaten Platzierungsvereinbarung fungierte. Aptevo hat sich verpflichtet, (1) bis zur früheren von Aktionärszustimmung oder 60 Tagen nach Abschluss keine weiteren Aktien auszugeben, und (2) für drei Monate keine variabel bepreisten Wertpapiervereinbarungen abzuschließen, vorbehaltlich üblicher Ausnahmen.

Verwendung der Erlöse: Betriebskapital, Finanzierung klinischer Programme und allgemeine Unternehmenszwecke, einschließlich der weiteren Entwicklung der Produktkandidaten.

Portfolio-Kommunikation: Zeitgleich wurden Pressemitteilungen veröffentlicht, die (i) Daten aus der laufenden Phase 1b/2 RAINIER-Studie zum CD123 × CD3 bispezifischen mipletamig bei AML und (ii) die Aufnahme des präklinischen Kandidaten APVO455 bekanntgaben, wodurch das CD3-orientierte Portfolio für hämatologische und solide Tumoren erweitert wird. Im Bericht wurden keine Wirksamkeits- oder Sicherheitsdaten enthalten.

Wichtige Erkenntnisse für Investoren

  • Ca. 7,45 Millionen US-Dollar neues Kapital verlängern die finanzielle Reichweite und unterstützen klinische Meilensteine.
  • Die Einheitenstruktur mit fünf hebelerzeugenden Stammoptionsscheinen bringt ein erhebliches potenzielles Verwässerungsrisiko (bis zu 12,3 Millionen Aktien) mit sich, falls die Aktionärszustimmung erteilt wird und die Optionsscheine ausgeübt werden.
  • Eine fehlende Zustimmung würde die Optionsscheine wertlos machen, was Investoren enttäuschen könnte, die auf den Optionsschein-Mehrwert gesetzt haben, aber die zukünftige Verwässerung für bestehende Aktionäre begrenzt.
  • Die Lock-up-Bestimmungen sind relativ kurz, begrenzen kurzfristige zusätzliche Emissionen, bieten jedoch keinen langfristigen Schutz.
  • Die Pipeline gewinnt mit dem neuen Kandidaten APVO455 und der laufenden mipletamig-Studie weiter an Fahrt, was auf Fortschritte in Forschung und Entwicklung hinweist, obwohl noch keine konkreten klinischen Daten veröffentlicht wurden.
Positive
  • Raised approximately $7.45 million in net proceeds, enhancing liquidity for ongoing clinical programs.
  • Expansion of pipeline through addition of pre-clinical candidate APVO455, signaling continued R&D investment.
  • No immediate shareholder dilution from common warrants until stockholder approval is obtained, providing interim protection.
Negative
  • Potential issuance of up to 12.3 million shares upon warrant exercise represents significant future dilution.
  • Stockholder approval risk: if approval is not obtained, warrants become worthless, creating uncertainty for investors and possible reputational impact.
  • Short lock-up periods (60 days for new issuance, three-month variable-price ban) limit long-term supply controls.

Insights

TL;DR: $7.45 M raise shores up liquidity but five-for-one warrant structure adds major dilution risk, leaving overall impact balanced.

The transaction injects much-needed cash for Aptevo’s clinical programs, important for a small-cap biotech without revenue. However, attaching 12.3 million common warrants to just 2.5 million primary securities creates a sizeable future overhang—roughly five times current shares issued through the raise—if stockholder approval is obtained. While the exercise price of $3.25 is above the unit price, the reset floor at $0.65 leaves downside protection for investors and potential dilution for existing holders. Short lock-ups (60 days / 3 months) further limit supply constraints. On the positive side, proceeds extend the cash runway and enable development of mipletamig and newly announced APVO455, maintaining momentum in the CD3 bispecific franchise. Net, the filing is capital-supportive yet dilutionary, producing a neutral rating.

TL;DR: Capital raise modestly strengthens balance sheet; warrant conditions create optionality but hinge on shareholder vote.

The Offering achieved roughly $7.45 million net, meaningful relative to Aptevo’s micro-cap size. Immediate exercisability of pre-funded warrants removes impediments to ownership limits, while delayed activation of common warrants ties future dilution to shareholder consent, aligning governance with Nasdaq rules. Strategic use of proceeds toward R&D supports value creation, and adding APVO455 broadens therapeutic optionality. Nonetheless, investors must weigh the 12.3 million potential warrant shares versus current float and the short prohibition on additional issuances. Should shares trade below $3.25, warrants risk remaining out-of-the-money, lessening dilution but weakening cash inflow potential. Overall, the event is modestly positive because it funds near-term catalysts without immediate massive share issuance.

Aptevo Therapeutics Inc. (NASDAQ: APVO) ha presentato un modulo 8-K per comunicare un aumento di capitale e aggiornamenti sul portafoglio prodotti. Il 18 giugno 2025 la Società ha firmato un Accordo di Acquisto di Titoli con investitori istituzionali per un'offerta diretta registrata (l’“Offerta”) che si è conclusa il 20 giugno 2025. La struttura prevedeva (i) 2.105.000 azioni ordinarie e (ii) warrant pre-finanziati per un massimo di 360.000 azioni, ciascuno venduto insieme a cinque warrant ordinari quinquennali (prezzo di esercizio $3,25). Il prezzo unitario era di $3,25 per azione o $3,249 per warrant pre-finanziato, riflettendo il prezzo di esercizio di $0,0001 sulla componente pre-finanziata.

I warrant ordinari non possono essere esercitati fino a quando non viene ottenuta l’approvazione degli azionisti secondo le regole del Nasdaq Capital Market; in caso contrario, i warrant diventano inesercitabili e privi di valore. Il prezzo di esercizio è soggetto a consueti aggiustamenti anti-diluizione ma non potrà scendere sotto $0,65. I warrant pre-finanziati sono esercitabili immediatamente a $0,001 per azione e rimangono validi fino al completo esercizio.

La Società ha ricevuto proventi netti di circa 7,45 milioni di dollari dopo aver dedotto le spese stimate dell’offerta e una commissione di collocamento del 7,0 % pagata a Roth Capital Partners, LLC, che ha agito come agente di collocamento esclusivo secondo un accordo separato. Aptevo si è impegnata (1) a non emettere ulteriori azioni fino al primo tra l’approvazione degli azionisti o 60 giorni dopo la chiusura, e (2) a non stipulare accordi su titoli a prezzo variabile per tre mesi, salvo eccezioni consuete.

Utilizzo dei proventi: capitale circolante, finanziamento di programmi clinici e scopi aziendali generali, inclusa la prosecuzione dello sviluppo dei candidati farmaceutici.

Aggiornamenti sul portafoglio: comunicati stampa paralleli hanno annunciato (i) dati dallo studio in corso di Fase 1b/2 RAINIER sul bispecifico CD123 × CD3 mipletamig in leucemia mieloide acuta (AML), e (ii) l’aggiunta del candidato pre-clinico APVO455, ampliando il portafoglio CD3 diretto a tumori ematologici e solidi. Nel deposito non sono stati inclusi dati di efficacia o sicurezza.

Punti chiave per gli investitori

  • Circa 7,45 milioni di dollari di nuovo capitale estendono la liquidità e supportano traguardi clinici.
  • La struttura dell’unità con cinque warrant ordinari a leva introduce un potenziale significativo rischio di diluizione (fino a 12,3 milioni di azioni) se si ottiene l’approvazione degli azionisti e i warrant vengono esercitati.
  • La mancata approvazione renderebbe i warrant privi di valore, deludendo gli investitori interessati al potenziale dei warrant ma limitando la diluizione futura per gli azionisti esistenti.
  • Le clausole di lock-up sono relativamente brevi, limitando ulteriori emissioni a breve termine ma non garantendo una protezione a lungo termine.
  • Il portafoglio continua a crescere con il nuovo candidato APVO455 e lo studio in corso su mipletamig, segnalando progressi nella R&S, anche se dati clinici concreti non sono ancora stati resi noti.

Aptevo Therapeutics Inc. (NASDAQ: APVO) presentó un formulario 8-K para revelar una ampliación de capital y varias actualizaciones de su cartera. El 18 de junio de 2025, la Compañía firmó un Acuerdo de Compra de Valores con inversores institucionales para una oferta directa registrada (la “Oferta”) que se cerró el 20 de junio de 2025. La estructura consistió en (i) 2.105.000 acciones comunes y (ii) warrants prefinanciados para hasta 360.000 acciones, cada uno vendido junto con cinco warrants comunes a cinco años (precio de ejercicio $3,25). El precio unitario fue $3,25 por acción o $3,249 por warrant prefinanciado, reflejando el precio de ejercicio de $0,0001 en la parte prefinanciada.

Los warrants comunes no pueden ejercerse hasta obtener la aprobación de los accionistas según las reglas del Nasdaq Capital Market; si no se obtiene dicha aprobación, los warrants se vuelven no ejercitables y sin valor. El precio de ejercicio está sujeto a ajustes anti-dilución habituales, pero no podrá bajar de $0,65. Los warrants prefinanciados son ejercitables inmediatamente a $0,001 por acción y permanecen vigentes hasta ser totalmente ejercidos.

La Compañía recibió ingresos netos de aproximadamente $7,45 millones después de deducir los gastos estimados de la oferta y una comisión de colocación del 7,0 % pagada a Roth Capital Partners, LLC, que actuó como agente exclusivo de colocación bajo un Acuerdo de Agencia de Colocación separado. Aptevo se comprometió (1) a no emitir acciones adicionales hasta la aprobación de los accionistas o 60 días después del cierre, lo que ocurra primero, y (2) a no celebrar acuerdos de valores con precio variable durante tres meses, sujeto a excepciones habituales.

Uso de los ingresos: capital de trabajo, financiación de programas clínicos y propósitos corporativos generales, incluyendo el desarrollo continuo de sus candidatos a productos.

Comunicaciones sobre la cartera: Comunicados de prensa simultáneos anunciaron (i) datos del ensayo en curso de Fase 1b/2 RAINIER del bispecífico CD123 × CD3 mipletamig en leucemia mieloide aguda (LMA), y (ii) la incorporación del candidato preclínico APVO455, ampliando la cartera dirigida a CD3 para tumores hematológicos y sólidos. No se incluyeron métricas de eficacia o seguridad en la presentación.

Puntos clave para inversores

  • Aproximadamente $7,45 millones en capital fresco extienden la pista financiera y apoyan hitos clínicos.
  • La estructura de la unidad con cinco warrants comunes apalancados introduce un potencial importante riesgo de dilución (hasta 12,3 millones de acciones) si se obtiene la aprobación de los accionistas y se ejercen los warrants.
  • La falta de aprobación haría que los warrants no tengan valor, lo que podría decepcionar a los inversores que apostaron por el potencial de los warrants, pero limitaría la dilución futura para los accionistas existentes.
  • Las disposiciones de bloqueo son relativamente cortas, limitando emisiones adicionales a corto plazo pero sin ofrecer protección a largo plazo.
  • El impulso de la cartera continúa con el nuevo candidato APVO455 y el estudio en curso de mipletamig, señalando progreso en I+D, aunque aún no se han divulgado datos clínicos concretos.

Aptevo Therapeutics Inc. (NASDAQ: APVO)는 자본 조달 및 포트폴리오 업데이트를 공개하기 위해 8-K 보고서를 제출했습니다. 2025년 6월 18일 회사는 기관 투자자들과 등록 직접 공모(“공모”)를 위한 증권 매매 계약을 체결했으며, 해당 공모는 2025년 6월 20일에 마감되었습니다. 구조는 (i) 보통주 2,105,000주와 (ii) 최대 360,000주에 대한 선행 자금 납입 워런트로 구성되었으며, 각각 5년 만기 보통주 워런트 5개(행사가 $3.25)와 함께 판매되었습니다. 단가(stock)는 주식 $3.25 또는 선행 자금 납입 워런트 $3.249로, 선행 자금 부분의 행사가 $0.0001을 반영합니다.

보통주 워런트는 Nasdaq Capital Market 규정에 따라 주주 승인이 있을 때까지 행사할 수 없으며, 승인이 없으면 워런트는 행사 불가능하며 가치가 없습니다. 행사가격은 통상적인 희석 방지 조정 대상이나 $0.65 아래로는 조정되지 않습니다. 선행 자금 납입 워런트는 주당 $0.001에 즉시 행사 가능하며 전부 행사될 때까지 유효합니다.

회사는 추정 공모 비용과 7.0% 배치 수수료를 Roth Capital Partners, LLC에 지급한 후 약 745만 달러의 순수익을 받았습니다. Roth Capital Partners는 별도의 배치 대행 계약에 따라 독점 배치 대행사로 활동했습니다. Aptevo는 (1) 주주 승인 또는 마감 후 60일 중 빠른 시점까지 추가 주식 발행을 하지 않으며, (2) 일반적인 예외를 제외하고 3개월간 변동 가격 증권 계약을 체결하지 않기로 합의했습니다.

수익금 사용처: 운전자본, 임상 프로그램 자금 조달 및 일반 기업 목적, 제품 후보군 개발 지속 포함.

파이프라인 소식: 동시 보도자료를 통해 (i) AML(급성 골수성 백혈병) 대상 CD123 × CD3 이중특이적 mipletamig의 진행 중인 1b/2상 RAINIER 시험 데이터, (ii) 혈액암 및 고형암 대상 CD3 지향 포트폴리오 확장을 위한 전임상 후보 APVO455 추가를 발표했습니다. 제출 자료에는 효능 또는 안전성 지표는 포함되지 않았습니다.

투자자를 위한 주요 요점

  • 약 745만 달러의 신규 자본이 자금 여력을 연장하고 임상 마일스톤을 지원합니다.
  • 5개의 레버리지 보통주 워런트가 포함된 단위 구조는 주주 승인 후 워런트 행사 시 최대 1,230만 주까지 상당한 희석 가능성을 내포합니다.
  • 승인 실패 시 워런트는 무가치해져 워런트 상승 잠재력을 기대한 투자자에게는 실망을 줄 수 있으나 기존 주주에겐 미래 희석을 제한합니다.
  • 락업 조항은 비교적 짧아 단기 추가 발행을 제한하지만 장기 보호는 제공하지 않습니다.
  • 신규 후보 APVO455와 진행 중인 mipletamig 연구로 파이프라인 모멘텀이 지속되고 있어 연구개발 진전을 시사하나 구체적인 임상 데이터는 아직 공개되지 않았습니다.

Aptevo Therapeutics Inc. (NASDAQ : APVO) a déposé un formulaire 8-K pour annoncer une levée de fonds et plusieurs mises à jour de son portefeuille. Le 18 juin 2025, la Société a signé un accord d'achat de titres avec des investisseurs institutionnels pour une offre directe enregistrée (l’« Offre ») qui s’est clôturée le 20 juin 2025. La structure comprenait (i) 2 105 000 actions ordinaires et (ii) des bons de souscription préfinancés pour jusqu’à 360 000 actions, chacun vendu avec cinq bons de souscription ordinaires d’une durée de cinq ans (prix d’exercice de 3,25 $). Le prix unitaire était de 3,25 $ pour l’action ou 3,249 $ pour le bon préfinancé, reflétant le prix d’exercice de 0,0001 $ sur la composante préfinancée.

Les bons ordinaires ne peuvent être exercés qu’après approbation des actionnaires conformément aux règles du Nasdaq Capital Market ; sans cette approbation, les bons deviennent inexerçables et sans valeur. Le prix d’exercice est soumis à des ajustements anti-dilution habituels mais ne pourra pas être inférieur à 0,65 $. Les bons préfinancés sont immédiatement exerçables à 0,001 $ par action et restent en circulation jusqu’à leur exercice complet.

La Société a reçu environ 7,45 millions de dollars nets après déduction des frais estimés de l’offre et d’une commission de placement de 7,0 % versée à Roth Capital Partners, LLC, qui a agi en tant qu’agent de placement exclusif dans le cadre d’un accord distinct. Aptevo s’est engagée (1) à ne pas émettre d’actions supplémentaires avant l’approbation des actionnaires ou 60 jours après la clôture, selon la première éventualité, et (2) à ne pas conclure d’accords sur des titres à prix variable pendant trois mois, sous réserve des exceptions habituelles.

Utilisation des fonds : fonds de roulement, financement des programmes cliniques et objectifs généraux de l’entreprise, y compris le développement continu de ses candidats produits.

Communications sur le portefeuille : Des communiqués de presse simultanés ont annoncé (i) des données de l’essai de phase 1b/2 RAINIER en cours sur le bispécifique CD123 × CD3 mipletamig dans la leucémie myéloïde aiguë (LMA), et (ii) l’ajout du candidat préclinique APVO455, élargissant le portefeuille dirigé contre CD3 pour les tumeurs hématologiques et solides. Aucun indicateur d’efficacité ou de sécurité n’a été inclus dans le dépôt.

Points clés pour les investisseurs

  • Environ 7,45 millions de dollars de capital frais prolongent la trésorerie et soutiennent les jalons cliniques.
  • La structure de l’unité avec cinq bons ordinaires à effet de levier introduit un risque important de dilution potentielle (jusqu’à 12,3 millions d’actions) si l’approbation des actionnaires est obtenue et que les bons sont exercés.
  • L’absence d’approbation rendrait les bons sans valeur, ce qui pourrait décevoir les investisseurs ayant parié sur le potentiel des bons mais limiterait la dilution future pour les actionnaires existants.
  • Les clauses de lock-up sont relativement courtes, limitant les émissions supplémentaires à court terme mais sans offrir de protection à long terme.
  • Le portefeuille progresse avec le nouveau candidat APVO455 et l’étude en cours sur mipletamig, indiquant des avancées en R&D, bien que des données cliniques concrètes ne soient pas encore divulguées.

Aptevo Therapeutics Inc. (NASDAQ: APVO) reichte ein 8-K ein, um eine Kapitalerhöhung und mehrere Portfolio-Updates bekannt zu geben. Am 18. Juni 2025 unterzeichnete das Unternehmen eine Wertpapierkaufvereinbarung mit institutionellen Investoren für ein registriertes Direktangebot (das „Angebot“), das am 20. Juni 2025 abgeschlossen wurde. Die Struktur bestand aus (i) 2.105.000 Stammaktien und (ii) vorfinanzierten Optionsscheinen für bis zu 360.000 Aktien, die jeweils zusammen mit fünf fünfjährigen Stammoptionsscheinen (Ausübungspreis 3,25 $) verkauft wurden. Der Stückpreis betrug 3,25 $ für Aktien bzw. 3,249 $ für einen vorfinanzierten Optionsschein, was den Ausübungspreis von 0,0001 $ für die vorfinanzierte Komponente widerspiegelt.

Die Stammoptionsscheine können erst ausgeübt werden, wenn die Zustimmung der Aktionäre gemäß den Regeln des Nasdaq Capital Market vorliegt; wird diese nicht erteilt, werden die Optionsscheine unverwertbar und wertlos. Der Ausübungspreis unterliegt üblichen Verwässerungsschutzanpassungen, wird jedoch nicht unter 0,65 $ zurückgesetzt. Vorfinanzierte Optionsscheine sind sofort zum Preis von 0,001 $ pro Aktie ausübbar und bleiben bis zur vollständigen Ausübung gültig.

Das Unternehmen erhielt Nettoerlöse von ca. 7,45 Millionen US-Dollar nach Abzug der geschätzten Angebotskosten und einer 7,0 %igen Platzierungsgebühr, die an Roth Capital Partners, LLC gezahlt wurde, die als exklusiver Platzierungsagent im Rahmen einer separaten Platzierungsvereinbarung fungierte. Aptevo hat sich verpflichtet, (1) bis zur früheren von Aktionärszustimmung oder 60 Tagen nach Abschluss keine weiteren Aktien auszugeben, und (2) für drei Monate keine variabel bepreisten Wertpapiervereinbarungen abzuschließen, vorbehaltlich üblicher Ausnahmen.

Verwendung der Erlöse: Betriebskapital, Finanzierung klinischer Programme und allgemeine Unternehmenszwecke, einschließlich der weiteren Entwicklung der Produktkandidaten.

Portfolio-Kommunikation: Zeitgleich wurden Pressemitteilungen veröffentlicht, die (i) Daten aus der laufenden Phase 1b/2 RAINIER-Studie zum CD123 × CD3 bispezifischen mipletamig bei AML und (ii) die Aufnahme des präklinischen Kandidaten APVO455 bekanntgaben, wodurch das CD3-orientierte Portfolio für hämatologische und solide Tumoren erweitert wird. Im Bericht wurden keine Wirksamkeits- oder Sicherheitsdaten enthalten.

Wichtige Erkenntnisse für Investoren

  • Ca. 7,45 Millionen US-Dollar neues Kapital verlängern die finanzielle Reichweite und unterstützen klinische Meilensteine.
  • Die Einheitenstruktur mit fünf hebelerzeugenden Stammoptionsscheinen bringt ein erhebliches potenzielles Verwässerungsrisiko (bis zu 12,3 Millionen Aktien) mit sich, falls die Aktionärszustimmung erteilt wird und die Optionsscheine ausgeübt werden.
  • Eine fehlende Zustimmung würde die Optionsscheine wertlos machen, was Investoren enttäuschen könnte, die auf den Optionsschein-Mehrwert gesetzt haben, aber die zukünftige Verwässerung für bestehende Aktionäre begrenzt.
  • Die Lock-up-Bestimmungen sind relativ kurz, begrenzen kurzfristige zusätzliche Emissionen, bieten jedoch keinen langfristigen Schutz.
  • Die Pipeline gewinnt mit dem neuen Kandidaten APVO455 und der laufenden mipletamig-Studie weiter an Fahrt, was auf Fortschritte in Forschung und Entwicklung hinweist, obwohl noch keine konkreten klinischen Daten veröffentlicht wurden.
false000167158400016715842025-06-182025-06-18

 

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 18, 2025

 

 

APTEVO THERAPEUTICS INC.

(Exact name of Registrant as Specified in Its Charter)

 

 

Delaware

001-37746

81-1567056

(State or Other Jurisdiction
of Incorporation)

(Commission File Number)

(IRS Employer
Identification No.)

 

 

 

 

 

2401 4th Avenue

Suite 1050

 

Seattle, Washington

 

98121

(Address of Principal Executive Offices)

 

(Zip Code)

 

Registrant’s Telephone Number, Including Area Code: (206) 838-0500

 

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

 

APVO

 

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.

On June 18, 2025, Aptevo Therapeutics Inc. (the "Company") entered into a securities purchase agreement (the “Purchase Agreement”) with certain institutional investors for the sale of (i) 2,105,000 shares of the Company’s common stock, par value $0.001 per share ("Common Stock") and (ii) pre-funded warrants ("Pre-funded Warrants") to purchase up to 360,000 shares of Common Stock. In addition, the Company sold to Investors common warrants to purchase up to 12,325,000 shares of Common Stock (the “Common Warrants” and together with the sale of Common Stock and Pre-funded Warrants, the “Offering”). The combined purchase price of one share of Common Stock and accompanying Common Warrants was $3.25 and the combined purchase price of a Pre-funded Warrant and accompanying Common Warrants was $3.249 which is equal to the purchase price per share of Common Stock and accompanying Common Warrants less the $0.0001 per share exercise price of each such Pre-funded Warrant. The closing of the Offering occurred on June 20, 2025 (the “Closing Date”).

Each share of Common Stock or Pre-funded Warrant in lieu thereof was offered together with five Common Warrants, each to purchase one share of Common Stock. The Common Warrants have an exercise price of $3.25 per share of Common Stock and will be exercisable beginning on the effective date of such stockholder approval as may be required by the applicable rules and regulations of the Nasdaq Capital Market (or any successor entity) to permit the exercise of the Common Warrants (“Stockholder Approval") and will expire five years from the date of Stockholder Approval. The exercise price of the Common Warrants is subject to adjustment for stock splits, share dividends, share combinations and similar capital transactions and at the Company’s discretion as further described in the Common Warrants; provided that the exercise price of the Common Warrants will not be adjusted to any price lower than $0.65 per share. In the event that the Company is unable to obtain the required Stockholder Approval, the Common Warrants will not be exercisable and therefore have no value.

Subject to certain ownership limitations described in the Pre-funded Warrants, the Pre-funded Warrants are immediately exercisable and have an exercise price of $0.001 per share of Common Stock. The Pre-funded Warrants may be exercised at any time until all of the Pre-funded Warrants are exercised in full.

The Purchase Agreement contains customary representations and warranties and agreements of the Company and the purchasers and customary indemnification rights and obligations of the parties. The Company has agreed to not issue any shares of Common Stock or securities exercisable or convertible into shares of Common Stock until the earlier of (i) the date of Stockholder Approval or (ii) sixty (60) days following the closing date of this offering, or enter into an agreement to issue securities at a future determined price, for a period of three (3) months following the closing of this offering, subject to certain exceptions.

In connection with the Offering, the Company entered into a Placement Agency Agreement (the "Placement Agency Agreement") on June 18, 2025 with Roth Capital Partners, LLC (the "Placement Agent"), as the exclusive placement agent in connection with the Offering. As compensation to the Placement Agent, the Company paid the Placement Agent a cash fee of 7.0% of the aggregate gross proceeds raised in the Offering and reimbursement of certain expenses.

The shares of Common Stock, the Common Warrants and the Pre-funded Warrants described above and the underlying shares of Common Stock were offered pursuant to the Registration Statement on Form S-1 (File No. 333-288061), which was declared effective by the Securities and Exchange Commission on June 18, 2025 and Form S-1MEF (File No. 333-288134) which was declared effective immediately upon filing on June 18, 2025.

 

The Company received net proceeds of approximately $7.45 million from the Offering, excluding the proceeds, if any, from the cash exercise of the Common Warrants and after deducting the estimated offering expenses payable by the Company, including the Placement Agent fees. The Company intends to use the net proceeds from the Offering for working capital to fund its clinical programs and general corporate purposes, including the further development of its product candidates.

The foregoing summaries of the Common Warrant, the Pre-funded Warrant, the Placement Agency Agreement and the Purchase Agreement do not purport to be complete and are subject to, and qualified in their entirety by, copies of such documents attached as Exhibits 4.1, 4.2, 10.1 and 10.2 to this Current Report on Form 8-K, which are incorporated herein by reference.

Item 8.01 Other Events.

The Company issued press releases announcing the Offering and the closing of the Offering on June 18 and June 20, 2025, respectively. Copies of these press releases are attached hereto as Exhibits 99.1 and 99.2, respectively, and are incorporated by reference into this Item 8.01 of this Current Report on Form 8-K.

On June 18, 2025, the Company issued a press release announcing data from the ongoing Phase 1b/2 RAINIER trial evaluating mipletamig, its first-in-class CD123 x CD3 bispecific antibody, in combination with standard-of-care venetoclax and azacitidine (ven/aza) for newly diagnosed patients with acute myeloid leukemia (AML) who are unfit for intensive chemotherapy. A copy of the press release is attached hereto as Exhibit 99.3 and is incorporated by reference herein.

 


On June 20, 2025, the Company issued a press release announcing that addition of preclinical candidate APVO455 to its growing portfolio of CD3-directed candidates built on the CRIS-7 derived CD3 binding domain—an approach demonstrating compelling potential across both hematologic and solid tumors. A copy of the press release is attached hereto as Exhibit 99.4 and is incorporated by reference herein.

 

Item 9.01 Financial Statements and Exhibits.

(d) Exhibits

The following exhibits are being filed herewith:

Exhibit No.

 

Description

4.1

 

Common Warrant, dated June 20, 2025.

4.2

 

Pre-funded Warrant, dated June 20, 2025.

10.1

 

Placement Agency Agreement, dated June 18, 2025, between the Company and Roth Capital Partners.

10.2

 

Securities Purchase Agreement, dated June 18, 2025, between the Company and the purchasers party thereto.

99.1

 

Press Release dated June 18, 2025.

99.2

 

Press Release dated June 20, 2025

99.3

 

Press Release dated June 18, 2025.

99.4

 

Press Release dated June 20, 2025.

104

 

Cover Page Interactive Data File (embedded within the Inline XBRL document)

 


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.

 

 

 

aptevo therapeutics inc.

 

 

 

 

Date:

June 20, 2025

By:

/s/ Marvin L. White

 

 

 

Marvin L. White
President and Chief Executive Officer

 


FAQ

How much capital did Aptevo Therapeutics (APVO) raise in June 2025?

The Company received approximately $7.45 million in net proceeds from the Offering that closed on 20 June 2025.

What is the structure and exercise price of the new common warrants issued by APVO?

Each unit included five common warrants with a $3.25 exercise price, exercisable for five years after required stockholder approval.

When do the pre-funded warrants become exercisable and at what price?

Pre-funded warrants are immediately exercisable at an exercise price of $0.001 per share and remain open until fully exercised.

What will Aptevo use the Offering proceeds for?

Management plans to allocate proceeds to working capital, clinical program funding, and general corporate purposes, including development of product candidates.

Who acted as placement agent and what fee did they receive?

Roth Capital Partners, LLC served as exclusive placement agent and was paid a 7 % cash fee on gross proceeds plus expense reimbursement.

What happens if Aptevo shareholders do not approve warrant exercisability?

If stockholder approval is not secured, the common warrants cannot be exercised and will have no value.
Aptevo Therapeutics Inc

NASDAQ:APVO

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Biotechnology
Pharmaceutical Preparations
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United States
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