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Omeros (OMER) investor relations material
Omeros Q4 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Closed a major asset purchase and license deal with Novo Nordisk for zaltenibart, securing $240 million upfront and up to $2.1 billion in total potential payments, plus royalties.
Achieved net income of $86.5 million ($1.22/share) in Q4 2025, reversing a net loss of $31.4 million in Q4 2024; full-year 2025 net loss narrowed to $3.4 million from $156.8 million in 2024.
Received FDA approval for YARTEMLEA (narsoplimab) as the first and only treatment for TA-TMA, with a broad label for adults and children over two; commercial launch began January 2026.
Launched YARTEMLEA in the U.S., achieving rapid formulary adoption and strong payer support.
Strengthened balance sheet by repaying all term loans and 2026 notes, leaving only 2029 convertible notes outstanding.
Financial highlights
Q4 2025 net income was $86.5 million ($1.22 per share), compared to a Q3 net loss of $30.9 million ($0.47 per share); non-GAAP adjusted Q4 net income was $222.5 million ($3.14 per share), excluding a $136 million non-cash charge.
Full-year 2025 non-GAAP adjusted net income was $133.4 million ($2.10/share).
Cash and investments at year-end 2025 totaled $171.8 million, up $135.7 million sequentially.
Aggregate principal debt reduced to $87.9 million at year-end 2025, down 47% from $164.9 million at year-end 2024.
OMIDRIA royalties in Q4 2025 were $9.2 million on $30.7 million U.S. net sales, down from $10.1 million on $33.6 million in Q4 2024.
Outlook and guidance
YARTEMLEA program expected to be financially self-sustaining in 2026; company targets positive cash flow in 2027, supported by Novo Nordisk partnership and YARTEMLEA commercialization.
No revenue guidance for YARTEMLEA provided due to early launch stage; focus remains on physician education and payer engagement.
Operating expenses in Q1 2026 expected to be similar to Q4 2025, with lower R&D and higher sales/marketing costs.
EMA decision for YARTEMLEA expected mid-2026 for EU market entry.
- Q3 net loss narrowed to $32.2M, but going concern risk persists as cash burn and debt remain high.OMER
Q3 202413 Feb 2026 - Q2 net loss rose on one-time costs; debt cut, OMIDRIA royalties up, clinical pipeline advanced.OMER
Q2 20242 Feb 2026 - FDA approved YARTEMLEA for TA-TMA, launching January 2026 with strong efficacy and safety.OMER
FDA Announcement8 Jan 2026 - Q4 net loss narrowed, cash at $90.1M, and major clinical milestones expected in 2025.OMER
Q4 202419 Dec 2025 - Proxy covers director elections, executive pay, auditor ratification, and 2024 business highlights.OMER
Proxy Filing2 Dec 2025 - Net loss narrowed, debt restructured, but liquidity risks remain as focus shifts to narsoplimab.OMER
Q1 202526 Nov 2025 - Q2 net loss improved, debt reduced, and narsoplimab regulatory reviews advanced.OMER
Q2 202523 Nov 2025 - Novo Nordisk deal and FDA decision on narsoplimab drive financial and strategic outlook.OMER
Q3 202517 Nov 2025
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