[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.
- 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.
(To Prospectus dated November 17, 2022)
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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 | | |
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Placement agent’s fees(1)
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| | | $ | 0.246 | | | | | $ | 1,320,000 | | |
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Proceeds to Omeros Corp. before expenses
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| | | $ | 3.854 | | | | | $ | 20,679,997 | | |
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About this Prospectus Supplement
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Forward-Looking Statements
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Prospectus Supplement Summary
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The Offering
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Risk Factors
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Use of Proceeds
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Dilution
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Plan of Distribution
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Legal Matters
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Experts
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Where You Can Find More Information
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Incorporation By Reference
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Page
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About this Prospectus
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Forward-Looking Statements
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About Omeros
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Where You Can Find More Information
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Incorporation by Reference
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Risk Factors
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Use of Proceeds
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Description of Common Stock
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Description of Preferred Stock
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Description of Debt Securities
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Description of Depository Shares
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Description of Warrants
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Description of Subscription Rights
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Description of Units
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Plan of Distribution
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Legal Matters
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Experts
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Product
Candidate/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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| | Narsoplimab (MASP-2 / Lectin Pathway) | | | TA-TMA | | |
BLA and MAA pending
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| | 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
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| | 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 | | |
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Net tangible book deficit per share as of March 31, 2025
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| | | $ | (3.68) | | | | | | | | |
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Increase in net tangible book value per share attributable in this offering
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| | | $ | 0.63 | | | | | | | | |
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As adjusted net tangible book deficit per share on March 31, 2025, after this offering
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| | | $ | (3.05) | | | | | | | | |
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Dilution per share to new investors purchasing our common stock in this offering
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| | | | | | | | | $ | 7.15 | | |
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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
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| | | $ | 0.246 | | | | | $ | 1,320,000 | | |
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Proceeds to Omeros Corp. before expenses
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| | | $ | 3.854 | | | | | $ | 20,679,997 | | |
Preferred Stock
Debt Securities
Depositary Shares
Warrants
Subscription Rights
Units
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Page
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| |||
|
About This Prospectus
|
| | | | ii | | |
|
Forward-Looking Statements
|
| | | | iii | | |
|
About Omeros
|
| | | | 1 | | |
|
Where You Can Find More Information
|
| | | | 2 | | |
|
Incorporation by Reference
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| | | | 2 | | |
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Risk Factors
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| | | | 3 | | |
|
Use of Proceeds
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| | | | 4 | | |
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Description of Common Stock
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| | | | 5 | | |
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Description of Preferred Stock
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| | | | 8 | | |
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Description of Debt Securities
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| | | | 10 | | |
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Description of Depositary Shares
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| | | | 20 | | |
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Description of Warrants
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| | | | 23 | | |
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Description of Subscription Rights
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| | | | 24 | | |
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Description of Units
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| | | | 25 | | |
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Plan of Distribution
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| | | | 26 | | |
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Legal Matters
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| | | | 29 | | |
|
Experts
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| | | | 29 | | |