SEC Form 424B5 filed by Omeros Corporation
(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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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
|
| | | $ | 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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