[424B5] Omeros Corporation Prospectus Supplement (Debt Securities)
Omeros (OMER) has entered into a registered direct offering of 5,365,853 common shares at $4.10, a 14% premium to the 24-Jul-25 close ($3.59). Gross proceeds total $22.0 million; after the 6% placement fee to D. Boral Capital ($1.32 million) and other expenses, net cash is expected at roughly $20.3 million.
The raise increases shares outstanding from 61.8 million to 67.1 million (≈8.7% dilution) and lifts available cash from ≈$26 million (18-Jul-25) to >$45 million, funding general corporate uses, clinical and pre-clinical pipeline work and working capital. Management retains broad spending discretion.
Key pipeline points: FDA’s BLA for lead MASP-2 antibody narsoplimab in TA-TMA now carries a 26-Dec-25 PDUFA date; EMA review is ongoing with an opinion expected mid-2026. The company is also advancing MASP-3 inhibitor zaltenibart (PNH, C3G) and PDE7 program OMS527 (cocaine use disorder). Omeros is negotiating a potential multi-billion-dollar asset deal that could retire its $67.1 million term loan and part of its 2026 notes.
Despite the premium pricing, the offer adds to a $(193 million) adjusted tangible book deficit and follows an auditor going-concern warning. Investors face immediate dilution of $7.15 per share (net tangible book value basis) and future overhang from 19.6 million outstanding options and convertible notes.
Omeros (OMER) ha avviato un'offerta diretta registrata di 5.365.853 azioni ordinarie a $4,10, con un premio del 14% rispetto alla chiusura del 24 luglio 2025 ($3,59). Il ricavato lordo ammonta a $22,0 milioni; dopo la commissione di collocamento del 6% a D. Boral Capital ($1,32 milioni) e altre spese, il netto in contanti previsto è di circa $20,3 milioni.
L’aumento porta il numero di azioni in circolazione da 61,8 milioni a 67,1 milioni (≈8,7% di diluizione) e incrementa la liquidità disponibile da circa $26 milioni (18 lug 2025) a oltre $45 milioni, finanziando usi aziendali generali, attività cliniche e precliniche del portafoglio e capitale circolante. Il management mantiene ampia discrezionalità nella spesa.
Punti chiave del portafoglio: la BLA della FDA per l’anticorpo MASP-2 di punta narsoplimab nel TA-TMA ha ora una data PDUFA al 26 dicembre 2025; la revisione EMA è in corso con un parere atteso a metà 2026. L’azienda sta inoltre sviluppando l’inibitore MASP-3 zaltenibart (PNH, C3G) e il programma PDE7 OMS527 (disturbo da uso di cocaina). Omeros sta negoziando un possibile accordo multi-miliardario che potrebbe estinguere il suo term loan da $67,1 milioni e parte delle note 2026.
Nonostante il prezzo con premio, l’offerta contribuisce a un deficit di patrimonio tangibile rettificato di $(193) milioni e segue un avviso dell’auditor sulla continuità aziendale. Gli investitori affrontano una diluizione immediata di $7,15 per azione (valore patrimoniale netto tangibile) e un potenziale sovraccarico futuro derivante da 19,6 milioni di opzioni e note convertibili in circolazione.
Omeros (OMER) ha iniciado una oferta directa registrada de 5.365.853 acciones ordinarias a $4,10, un 14% por encima del cierre del 24 de julio de 2025 ($3,59). Los ingresos brutos totalizan $22,0 millones; tras la comisión de colocación del 6% a D. Boral Capital ($1,32 millones) y otros gastos, se espera un efectivo neto de aproximadamente $20,3 millones.
La ampliación aumenta las acciones en circulación de 61,8 millones a 67,1 millones (≈8,7% de dilución) y eleva el efectivo disponible de ≈$26 millones (18-jul-25) a más de $45 millones, financiando usos corporativos generales, trabajos clínicos y preclínicos del pipeline y capital de trabajo. La dirección mantiene amplia discreción en el gasto.
Puntos clave del pipeline: la BLA de la FDA para el anticuerpo líder MASP-2 narsoplimab en TA-TMA tiene ahora una fecha PDUFA para el 26-dic-25; la revisión de la EMA está en curso con un dictamen esperado a mediados de 2026. La compañía también está avanzando con el inhibidor MASP-3 zaltenibart (PNH, C3G) y el programa PDE7 OMS527 (trastorno por consumo de cocaína). Omeros está negociando un posible acuerdo de activos multimillonario que podría cancelar su préstamo a plazo de $67,1 millones y parte de sus notas 2026.
A pesar del precio con prima, la oferta añade a un déficit ajustado de valor en libros tangible de $(193) millones y sigue a una advertencia del auditor sobre la continuidad operativa. Los inversores enfrentan una dilución inmediata de $7,15 por acción (base valor en libros tangible neto) y una futura sobrecarga por 19,6 millones de opciones y notas convertibles en circulación.
Omeros(OMER)는 5,365,853주 보통주를 주당 $4.10에 등록 직접 공모로 발행했으며, 이는 2025년 7월 24일 종가($3.59) 대비 14% 프리미엄입니다. 총 조달 금액은 $2200만이며, D. Boral Capital에 지급하는 6% 배치 수수료($132만) 및 기타 비용을 제외한 순현금은 약 $2030만으로 예상됩니다.
이번 자금 조달로 발행 주식 수가 6180만 주에서 6710만 주로 증가(약 8.7% 희석)하고, 사용 가능한 현금은 2025년 7월 18일 기준 약 2600만 달러에서 4500만 달러 이상으로 늘어나 일반 기업 운영, 임상 및 전임상 파이프라인 연구, 운전자본에 자금을 지원합니다. 경영진은 광범위한 지출 재량을 유지합니다.
주요 파이프라인 사항: FDA의 BLA(생물학적 허가 신청)에서 선도 MASP-2 항체 narsoplimab의 TA-TMA 적응증에 대해 2025년 12월 26일 PDUFA(허가 결정) 날짜가 지정되었으며, EMA 심사는 진행 중이며 2026년 중반 의견이 예상됩니다. 회사는 MASP-3 억제제 zaltenibart(PNH, C3G)와 PDE7 프로그램 OMS527(코카인 사용 장애)도 개발 중입니다. Omeros는 다수십억 달러 규모의 자산 거래를 협상 중이며, 이를 통해 $6710만의 장기 대출과 2026년 채권 일부를 상환할 수 있습니다.
프리미엄 가격임에도 불구하고 이번 공모는 조정된 유형 자산 장부가치 적자 $(1억 9300만)를 증가시키며, 감사인의 계속기업 경고 이후 이루어졌습니다. 투자자들은 주당 $7.15의 즉각적인 희석(순유형자산 장부가치 기준)과 1,960만 주의 미행사 옵션 및 전환 사채에서 오는 미래 부담을 감수해야 합니다.
Omeros (OMER) a lancé une offre directe enregistrée portant sur 5 365 853 actions ordinaires à 4,10 $, soit une prime de 14 % par rapport à la clôture du 24 juillet 2025 (3,59 $). Le produit brut s’élève à 22,0 millions de dollars ; après la commission de placement de 6 % versée à D. Boral Capital (1,32 million de dollars) et autres frais, le produit net attendu est d’environ 20,3 millions de dollars.
Cette levée porte le nombre d’actions en circulation de 61,8 millions à 67,1 millions (≈8,7 % de dilution) et augmente la trésorerie disponible d’environ 26 millions de dollars (au 18 juillet 2025) à plus de 45 millions, finançant les usages généraux de l’entreprise, les travaux cliniques et précliniques du pipeline ainsi que le fonds de roulement. La direction conserve une large discrétion dans les dépenses.
Points clés du pipeline : la BLA de la FDA pour l’anticorps principal MASP-2 narsoplimab dans le TA-TMA a désormais une date PDUFA fixée au 26 décembre 2025 ; l’examen par l’EMA est en cours avec un avis attendu à la mi-2026. La société fait également progresser l’inhibiteur MASP-3 zaltenibart (PNH, C3G) et le programme PDE7 OMS527 (trouble lié à la consommation de cocaïne). Omeros négocie un potentiel accord d’actifs de plusieurs milliards de dollars qui pourrait rembourser son prêt à terme de 67,1 millions de dollars ainsi qu’une partie de ses obligations 2026.
Malgré le prix avec prime, l’offre accroît un déficit ajusté du fonds propres tangible de (193) millions de dollars et fait suite à un avertissement de continuité d’exploitation de l’auditeur. Les investisseurs font face à une dilution immédiate de 7,15 $ par action (sur la base de la valeur comptable tangible nette) ainsi qu’à une pression future due à 19,6 millions d’options et obligations convertibles en circulation.
Omeros (OMER) hat eine registrierte Direktplatzierung von 5.365.853 Stammaktien zu je $4,10 durchgeführt, was einem Aufschlag von 14 % gegenüber dem Schlusskurs am 24. Juli 2025 ($3,59) entspricht. Der Bruttoerlös beträgt $22,0 Millionen; nach Abzug der 6 % Platzierungsgebühr an D. Boral Capital ($1,32 Millionen) und sonstiger Kosten wird ein Nettobarmittelzufluss von rund $20,3 Millionen erwartet.
Die Kapitalerhöhung erhöht die ausstehenden Aktien von 61,8 Millionen auf 67,1 Millionen (≈8,7 % Verwässerung) und steigert die verfügbaren liquiden Mittel von etwa $26 Millionen (18. Juli 2025) auf über $45 Millionen, zur Finanzierung von allgemeinen Unternehmenszwecken, klinischer und präklinischer Pipeline-Arbeit sowie Betriebskapital. Das Management behält eine breite Ausgabendisposition bei.
Wesentliche Pipeline-Punkte: Der FDA-BLA für den führenden MASP-2-Antikörper narsoplimab bei TA-TMA hat nun ein PDUFA-Datum am 26. Dezember 2025; die EMA-Prüfung läuft und eine Stellungnahme wird Mitte 2026 erwartet. Das Unternehmen entwickelt zudem den MASP-3-Inhibitor zaltenibart (PNH, C3G) und das PDE7-Programm OMS527 (Kokaingebrauchsstörung) weiter. Omeros verhandelt über einen potenziellen milliardenschweren Asset-Deal, der seinen $67,1 Millionen Terminkredit und einen Teil seiner 2026er Anleihen tilgen könnte.
Trotz des Premium-Preises erhöht das Angebot ein bereinigtes negatives materielles Buchwertdefizit von $(193) Millionen und folgt einer Going-Concern-Warnung des Wirtschaftsprüfers. Anleger sehen sich einer sofortigen Verwässerung von $7,15 je Aktie (basierend auf dem bereinigten materiellen Buchwert) sowie einem zukünftigen Überhang von 19,6 Millionen ausstehenden Optionen und Wandelanleihen gegenüber.
- Premium pricing: Shares sold at $4.10, 14% above prior close, limiting price pressure.
- Liquidity boost: ≈$20.3 million net proceeds nearly doubles available cash, funding operations toward key FDA/EMA milestones.
- Supports pipeline: Capital earmarked for narsoplimab, zaltenibart and other programs, sustaining value-creating activities.
- Potential large partnership: Ongoing talks could generate enough cash to repay debt and extend runway materially.
- Dilution: Share count rises 8.7%, with further dilution possible from 19.6 million options and convertible notes.
- Persisting deficit: Adjusted tangible book value remains negative (-$193 million) even after the raise.
- Going-concern risk: Auditor highlighted substantial doubt about continuing operations.
- Regulatory timing risk: Narsoplimab PDUFA date pushed to 26-Dec-25, creating additional uncertainty.
Insights
TL;DR – Capital raise priced at a premium boosts liquidity but adds 9% dilution.
The $20 million net raise meaningfully extends a strained cash runway ($26 million at 18-Jul-25) while management pursues a larger asset-monetisation deal. Pricing above market signals strong institutional demand and mitigates near-term price pressure. However, tangible book value remains deeply negative, and the new shares lift fully diluted count beyond 90 million when options and convertibles are considered. The financing buys time to reach the December PDUFA decision on narsoplimab; if approval slips, further dilution is likely. Overall impact: modestly positive for liquidity, neutral for valuation.
TL;DR – Small cash infusion bridges to key catalysts but risk profile unchanged.
Proceeds cover roughly two quarters of burn, allowing Omeros to keep its pipeline alive without shuttering programs ahead of the narsoplimab verdict. The premium pricing and single-investor structure avoid a broad market discount, yet the company’s going-concern disclosure and debt load persist. Success hinges on FDA approval and/or sealing the hinted multi-billion partnership. Failure on either front would quickly erode the benefit of this raise. Thus, the event is tactically helpful but not materially de-risking.
Omeros (OMER) ha avviato un'offerta diretta registrata di 5.365.853 azioni ordinarie a $4,10, con un premio del 14% rispetto alla chiusura del 24 luglio 2025 ($3,59). Il ricavato lordo ammonta a $22,0 milioni; dopo la commissione di collocamento del 6% a D. Boral Capital ($1,32 milioni) e altre spese, il netto in contanti previsto è di circa $20,3 milioni.
L’aumento porta il numero di azioni in circolazione da 61,8 milioni a 67,1 milioni (≈8,7% di diluizione) e incrementa la liquidità disponibile da circa $26 milioni (18 lug 2025) a oltre $45 milioni, finanziando usi aziendali generali, attività cliniche e precliniche del portafoglio e capitale circolante. Il management mantiene ampia discrezionalità nella spesa.
Punti chiave del portafoglio: la BLA della FDA per l’anticorpo MASP-2 di punta narsoplimab nel TA-TMA ha ora una data PDUFA al 26 dicembre 2025; la revisione EMA è in corso con un parere atteso a metà 2026. L’azienda sta inoltre sviluppando l’inibitore MASP-3 zaltenibart (PNH, C3G) e il programma PDE7 OMS527 (disturbo da uso di cocaina). Omeros sta negoziando un possibile accordo multi-miliardario che potrebbe estinguere il suo term loan da $67,1 milioni e parte delle note 2026.
Nonostante il prezzo con premio, l’offerta contribuisce a un deficit di patrimonio tangibile rettificato di $(193) milioni e segue un avviso dell’auditor sulla continuità aziendale. Gli investitori affrontano una diluizione immediata di $7,15 per azione (valore patrimoniale netto tangibile) e un potenziale sovraccarico futuro derivante da 19,6 milioni di opzioni e note convertibili in circolazione.
Omeros (OMER) ha iniciado una oferta directa registrada de 5.365.853 acciones ordinarias a $4,10, un 14% por encima del cierre del 24 de julio de 2025 ($3,59). Los ingresos brutos totalizan $22,0 millones; tras la comisión de colocación del 6% a D. Boral Capital ($1,32 millones) y otros gastos, se espera un efectivo neto de aproximadamente $20,3 millones.
La ampliación aumenta las acciones en circulación de 61,8 millones a 67,1 millones (≈8,7% de dilución) y eleva el efectivo disponible de ≈$26 millones (18-jul-25) a más de $45 millones, financiando usos corporativos generales, trabajos clínicos y preclínicos del pipeline y capital de trabajo. La dirección mantiene amplia discreción en el gasto.
Puntos clave del pipeline: la BLA de la FDA para el anticuerpo líder MASP-2 narsoplimab en TA-TMA tiene ahora una fecha PDUFA para el 26-dic-25; la revisión de la EMA está en curso con un dictamen esperado a mediados de 2026. La compañía también está avanzando con el inhibidor MASP-3 zaltenibart (PNH, C3G) y el programa PDE7 OMS527 (trastorno por consumo de cocaína). Omeros está negociando un posible acuerdo de activos multimillonario que podría cancelar su préstamo a plazo de $67,1 millones y parte de sus notas 2026.
A pesar del precio con prima, la oferta añade a un déficit ajustado de valor en libros tangible de $(193) millones y sigue a una advertencia del auditor sobre la continuidad operativa. Los inversores enfrentan una dilución inmediata de $7,15 por acción (base valor en libros tangible neto) y una futura sobrecarga por 19,6 millones de opciones y notas convertibles en circulación.
Omeros(OMER)는 5,365,853주 보통주를 주당 $4.10에 등록 직접 공모로 발행했으며, 이는 2025년 7월 24일 종가($3.59) 대비 14% 프리미엄입니다. 총 조달 금액은 $2200만이며, D. Boral Capital에 지급하는 6% 배치 수수료($132만) 및 기타 비용을 제외한 순현금은 약 $2030만으로 예상됩니다.
이번 자금 조달로 발행 주식 수가 6180만 주에서 6710만 주로 증가(약 8.7% 희석)하고, 사용 가능한 현금은 2025년 7월 18일 기준 약 2600만 달러에서 4500만 달러 이상으로 늘어나 일반 기업 운영, 임상 및 전임상 파이프라인 연구, 운전자본에 자금을 지원합니다. 경영진은 광범위한 지출 재량을 유지합니다.
주요 파이프라인 사항: FDA의 BLA(생물학적 허가 신청)에서 선도 MASP-2 항체 narsoplimab의 TA-TMA 적응증에 대해 2025년 12월 26일 PDUFA(허가 결정) 날짜가 지정되었으며, EMA 심사는 진행 중이며 2026년 중반 의견이 예상됩니다. 회사는 MASP-3 억제제 zaltenibart(PNH, C3G)와 PDE7 프로그램 OMS527(코카인 사용 장애)도 개발 중입니다. Omeros는 다수십억 달러 규모의 자산 거래를 협상 중이며, 이를 통해 $6710만의 장기 대출과 2026년 채권 일부를 상환할 수 있습니다.
프리미엄 가격임에도 불구하고 이번 공모는 조정된 유형 자산 장부가치 적자 $(1억 9300만)를 증가시키며, 감사인의 계속기업 경고 이후 이루어졌습니다. 투자자들은 주당 $7.15의 즉각적인 희석(순유형자산 장부가치 기준)과 1,960만 주의 미행사 옵션 및 전환 사채에서 오는 미래 부담을 감수해야 합니다.
Omeros (OMER) a lancé une offre directe enregistrée portant sur 5 365 853 actions ordinaires à 4,10 $, soit une prime de 14 % par rapport à la clôture du 24 juillet 2025 (3,59 $). Le produit brut s’élève à 22,0 millions de dollars ; après la commission de placement de 6 % versée à D. Boral Capital (1,32 million de dollars) et autres frais, le produit net attendu est d’environ 20,3 millions de dollars.
Cette levée porte le nombre d’actions en circulation de 61,8 millions à 67,1 millions (≈8,7 % de dilution) et augmente la trésorerie disponible d’environ 26 millions de dollars (au 18 juillet 2025) à plus de 45 millions, finançant les usages généraux de l’entreprise, les travaux cliniques et précliniques du pipeline ainsi que le fonds de roulement. La direction conserve une large discrétion dans les dépenses.
Points clés du pipeline : la BLA de la FDA pour l’anticorps principal MASP-2 narsoplimab dans le TA-TMA a désormais une date PDUFA fixée au 26 décembre 2025 ; l’examen par l’EMA est en cours avec un avis attendu à la mi-2026. La société fait également progresser l’inhibiteur MASP-3 zaltenibart (PNH, C3G) et le programme PDE7 OMS527 (trouble lié à la consommation de cocaïne). Omeros négocie un potentiel accord d’actifs de plusieurs milliards de dollars qui pourrait rembourser son prêt à terme de 67,1 millions de dollars ainsi qu’une partie de ses obligations 2026.
Malgré le prix avec prime, l’offre accroît un déficit ajusté du fonds propres tangible de (193) millions de dollars et fait suite à un avertissement de continuité d’exploitation de l’auditeur. Les investisseurs font face à une dilution immédiate de 7,15 $ par action (sur la base de la valeur comptable tangible nette) ainsi qu’à une pression future due à 19,6 millions d’options et obligations convertibles en circulation.
Omeros (OMER) hat eine registrierte Direktplatzierung von 5.365.853 Stammaktien zu je $4,10 durchgeführt, was einem Aufschlag von 14 % gegenüber dem Schlusskurs am 24. Juli 2025 ($3,59) entspricht. Der Bruttoerlös beträgt $22,0 Millionen; nach Abzug der 6 % Platzierungsgebühr an D. Boral Capital ($1,32 Millionen) und sonstiger Kosten wird ein Nettobarmittelzufluss von rund $20,3 Millionen erwartet.
Die Kapitalerhöhung erhöht die ausstehenden Aktien von 61,8 Millionen auf 67,1 Millionen (≈8,7 % Verwässerung) und steigert die verfügbaren liquiden Mittel von etwa $26 Millionen (18. Juli 2025) auf über $45 Millionen, zur Finanzierung von allgemeinen Unternehmenszwecken, klinischer und präklinischer Pipeline-Arbeit sowie Betriebskapital. Das Management behält eine breite Ausgabendisposition bei.
Wesentliche Pipeline-Punkte: Der FDA-BLA für den führenden MASP-2-Antikörper narsoplimab bei TA-TMA hat nun ein PDUFA-Datum am 26. Dezember 2025; die EMA-Prüfung läuft und eine Stellungnahme wird Mitte 2026 erwartet. Das Unternehmen entwickelt zudem den MASP-3-Inhibitor zaltenibart (PNH, C3G) und das PDE7-Programm OMS527 (Kokaingebrauchsstörung) weiter. Omeros verhandelt über einen potenziellen milliardenschweren Asset-Deal, der seinen $67,1 Millionen Terminkredit und einen Teil seiner 2026er Anleihen tilgen könnte.
Trotz des Premium-Preises erhöht das Angebot ein bereinigtes negatives materielles Buchwertdefizit von $(193) Millionen und folgt einer Going-Concern-Warnung des Wirtschaftsprüfers. Anleger sehen sich einer sofortigen Verwässerung von $7,15 je Aktie (basierend auf dem bereinigten materiellen Buchwert) sowie einem zukünftigen Überhang von 19,6 Millionen ausstehenden Optionen und Wandelanleihen gegenüber.
(To Prospectus dated November 17, 2022)
![[MISSING IMAGE: lg_omeroswithoutreg-4c.jpg]](https://www.sec.gov/Archives/edgar/data/0001285819/000110465925070553/lg_omeroswithoutreg-4c.jpg)
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Per Share
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Total
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Purchase price
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| | | $ | 4.10 | | | | | $ | 21,999,997 | | |
Placement agent’s fees(1)
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| | | $ | 0.246 | | | | | $ | 1,320,000 | | |
Proceeds to Omeros Corp. before expenses
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| | | $ | 3.854 | | | | | $ | 20,679,997 | | |
![[MISSING IMAGE: lg_dboralcapital-4c.jpg]](https://www.sec.gov/Archives/edgar/data/0001285819/000110465925070553/lg_dboralcapital-4c.jpg)
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About this Prospectus Supplement
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| | | | S-ii | | |
Forward-Looking Statements
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| | | | S-iii | | |
Prospectus Supplement Summary
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| | | | S-1 | | |
The Offering
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| | | | S-5 | | |
Risk Factors
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| | | | S-6 | | |
Use of Proceeds
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| | | | S-9 | | |
Dilution
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| | | | S-10 | | |
Plan of Distribution
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| | | | S-11 | | |
Legal Matters
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| | | | S-12 | | |
Experts
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| | | | S-12 | | |
Where You Can Find More Information
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| | | | S-12 | | |
Incorporation By Reference
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| | | | S-13 | | |
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Page
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About this Prospectus
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| | | | ii | | |
Forward-Looking Statements
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| | | | iii | | |
About Omeros
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| | | | 1 | | |
Where You Can Find More Information
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Incorporation by Reference
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Risk Factors
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| | | | 3 | | |
Use of Proceeds
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| | | | 4 | | |
Description of Common Stock
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| | | | 5 | | |
Description of Preferred Stock
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| | | | 8 | | |
Description of Debt Securities
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| | | | 10 | | |
Description of Depository Shares
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| | | | 20 | | |
Description of Warrants
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| | | | 23 | | |
Description of Subscription Rights
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| | | | 24 | | |
Description of Units
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| | | | 25 | | |
Plan of Distribution
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| | | | 26 | | |
Legal Matters
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| | | | 29 | | |
Experts
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| | | | 29 | | |
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Product
Candidate/Program |
| |
Targeted Disease(s)
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| |
Development Status
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Next Expected
Milestone |
|
| Narsoplimab (MASP-2 / Lectin Pathway) | | | TA-TMA | | |
BLA and MAA pending
|
| | Regulatory agency review of BLA and MAA | |
| Narsoplimab (MASP-2 / Lectin Pathway) | | | Severe COVID-19, post-acute sequelae of SARS-CoV-2 infection (PASC, i.e., long COVID) and other causes of acute respiratory distress syndrome (ARDS) | | | Phase 2 trial in severe COVID-19 completed | | | Continue development of narsoplimab and diagnostic for lectin pathway hyperactivation for ARDS and related indications | |
| OMS1029 (MASP-2 / Lectin Pathway) | | | Long-acting second-generation antibody targeting lectin pathway disorders | | | Phase 1 studies completed | | | Select indication for Phase 2 development | |
| Zaltenibart (MASP-3 / Alternative Pathway) | | | Paroxysmal nocturnal hemoglobinuria (PNH) | | | Phase 3 programs initiated | | | Restart Phase 3 clinical trials | |
| Zaltenibart (MASP-3 / Alternative Pathway) | | | C3G and other alternative pathway disorders | | | Phase 2 program ongoing | | |
Complete Phase 2 study
|
|
| OMS527 (PDE7) | | | Cocaine use disorder (CUD); other addictive and compulsive disorders; movement disorders | | | Phase 1b study in adult cocaine users awaiting initiation with already committed funding from National Institute on Drug Abuse (NIDA) | | | Complete NIDA-funded Phase 1b clinical trial in cocaine users | |
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Preclinical Program
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Targeted Disease(s)
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Development
Status |
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Next Expected
Milestone |
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| MASP-2: small-molecule inhibitors | | | Lectin pathway disorders | | | Preclinical | | | Assess preclinical data on current drug development candidate | |
| MASP-3: small-molecule inhibitors | | | Alternative pathway disorders | | | Preclinical | | | Identify drug development candidate for clinical trials | |
| Adoptive T-Cell and Immunostimulator Combination Therapies | | | Wide range of cancers | | | Preclinical | | | Complete preclinical proof of concept studies and evaluate data | |
| Oncotoxins and Immunomodulators | | | Wide range of cancers | | | Preclinical | | | Complete preclinical proof of concept studies and evaluate data | |
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Offering price per share
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| | | | | | | | | $ | 4.10 | | |
|
Net tangible book deficit per share as of March 31, 2025
|
| | | $ | (3.68) | | | | | | | | |
|
Increase in net tangible book value per share attributable in this offering
|
| | | $ | 0.63 | | | | | | | | |
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As adjusted net tangible book deficit per share on March 31, 2025, after this offering
|
| | | $ | (3.05) | | | | | | | | |
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Dilution per share to new investors purchasing our common stock in this offering
|
| | | | | | | | | $ | 7.15 | | |
| | |
Per Share
|
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Total
|
| ||||||
Purchase price
|
| | | $ | 4.10 | | | | | $ | 21,999,997 | | |
Placement agent’s fees
|
| | | $ | 0.246 | | | | | $ | 1,320,000 | | |
Proceeds to Omeros Corp. before expenses
|
| | | $ | 3.854 | | | | | $ | 20,679,997 | | |
![[MISSING IMAGE: lg_omeros-4c.jpg]](https://www.sec.gov/Archives/edgar/data/0001285819/000110465925070553/lg_omeros-4c.jpg)
Preferred Stock
Debt Securities
Depositary Shares
Warrants
Subscription Rights
Units
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Page
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About This Prospectus
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| | | | ii | | |
Forward-Looking Statements
|
| | | | iii | | |
About Omeros
|
| | | | 1 | | |
Where You Can Find More Information
|
| | | | 2 | | |
Incorporation by Reference
|
| | | | 2 | | |
Risk Factors
|
| | | | 3 | | |
Use of Proceeds
|
| | | | 4 | | |
Description of Common Stock
|
| | | | 5 | | |
Description of Preferred Stock
|
| | | | 8 | | |
Description of Debt Securities
|
| | | | 10 | | |
Description of Depositary Shares
|
| | | | 20 | | |
Description of Warrants
|
| | | | 23 | | |
Description of Subscription Rights
|
| | | | 24 | | |
Description of Units
|
| | | | 25 | | |
Plan of Distribution
|
| | | | 26 | | |
Legal Matters
|
| | | | 29 | | |
Experts
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| | | | 29 | | |
![[MISSING IMAGE: lg_omeroswithoutreg-4c.jpg]](https://www.sec.gov/Archives/edgar/data/0001285819/000110465925070553/lg_omeroswithoutreg-4c.jpg)
![[MISSING IMAGE: lg_dboralcapital-4c.jpg]](https://www.sec.gov/Archives/edgar/data/0001285819/000110465925070553/lg_dboralcapital-4c.jpg)