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Forecast

The analysts' average price target is €24.69 (+55.77%). The median is €24.69 (+55.77%).

Buy	12
Hold	5
Sell	2

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Omeros benefits from Yartemlea launch after FDA approval and beats quarterly expectations

Omeros reported adjusted earnings of $0.02 per share and net revenue of $28.5 million for the second quarter, well above expectations. The main driver was the commercial launch of the FDA‑approved antibody Yartemlea for the treatment of TA‑TMA, giving the company a monopoly position. Omeros also generated positive operating cash flow of $4.1 million. » More on finanzen.net
Omeros reaches 52-week high of $18.16 after strong quarterly results

Omeros shares rose to a new 52-week high of $18.16, lifting market capitalization to around $1.31 billion. In the second quarter the company comfortably beat analysts’ expectations with adjusted earnings of $0.02 per share and revenue of $28.5 million, supported by the launch of YARTEMLEA. Data from InvestingPro point to an overbought RSI level and a possible overvaluation of the stock. » More on de.investing.com
Omeros beats Q2 forecasts thanks to YARTEMLEA, stock rises 20%

Omeros reported adjusted earnings of $0.02 per share and revenue of $28.5 million for Q2 2026, well above consensus estimates. Gross product revenue from YARTEMLEA was $32.2 million in the first full quarter of launch and contributed materially to positive operating cash flow of $4.1 million. Management expects higher selling and R&D expenses in Q3 but provided no revenue guidance; the stock rose about 20% in after-hours trading. » More on de.investing.com
Omeros receives negative CHMP opinion on narsoplimab, will seek reconsideration

After an oral explanation meeting the CHMP adopted a negative opinion on Omeros' narsoplimab marketing application. Omeros plans to request reconsideration and an assessment by an EMA Ad Hoc Expert Panel. H.C. Wainwright cut its price target from $40 to $33 but kept a Buy rating, citing the U.S. launch as the key value driver. » More on finance.yahoo.com
Omeros announces repurchase of convertible notes of up to $16 million

Omeros has entered privately negotiated agreements to repurchase its 9.50% convertible notes due 2029 with a principal amount of up to about $16 million; the total purchase price including interest is expected to be up to about $34 million and will be partly determined by the share price during an upcoming averaging period. The repurchases are expected to settle between July 6 and 16; if fully repurchased, about $54.8 million in principal would remain outstanding. At the same time, Omeros significantly missed expectations for revenue and EPS in Q1 2026, while H.C. Wainwright remains at a buy rating with a $40 price target and highlights key data releases due mid‑2026. » More on de.investing.com

Historical dividends Dividends

All dividend metrics All metrics

In 2022, Omeros Co. has already paid €0.94 in dividends. The last payout was in May 2022.

Financials

In the last quarter, Omeros Co. had revenue of €25M and net profit of €11.59M

(EUR)	June 2026	YoY
Revenue	25M	-
Gross profit	24.3M	378.24%
Net profit	11.59M	153.75%
EBITDA	12.66M	158.10%

Fundamentals

Metric	Value
Market capitalization	€1.12B
Number of shares	72.39M
52-week high/low	€19.07 - €5.60
Dividends	No
Beta	2.57
P/E ratio	9.01
PEG ratio	0.00
P/B ratio	-24.16
P/S ratio	32.41

Company profile

Omeros Corporation, a commercial-stage biopharmaceutical company, discovers, develops, and commercializes small-molecule and protein therapeutics, and orphan indications targeting inflammation, complement-mediated diseases, cancers related to dysfunction of the immune system, and addictive and compulsive disorders. The company's clinical programs include Narsoplimab (OMS721/MASP-2) that has completed pivotal studies for hematopoietic stem-cell transplant-associated thrombotic microangiopathy (HSCT-TMA); that is in Phase III clinical trial for immunoglobulin A nephropathy (IgAN) and atypical hemolytic uremic syndrome (aHUS); and Phase II clinical trial to treat COVID-19. Its clinical programs also consist of PPAR? (OMS405) that is in Phase II to treat opioid and nicotine addiction; PDE7 (OMS527), which is in Phase I trial for treating addiction and compulsive disorders, and movement disorders; and MASP-3 (OMS906) that is in Phase I trial for paroxysmal nocturnal hemoglobinuria (PNH) and other alternative pathway disorders. The company's preclinical programs comprise MASP-2-small-molecule inhibitors used for the treatment of aHUS, IgAN, HSCT-TMA, and age-related macular degeneration; longer-acting second generation antibody targeting MASP-2; and MASP-3-small-molecule inhibitors to treat PNH and other alternative pathway disorders. Its preclinical programs also include GPR174 Inhibitors and Chimeric Antigen Receptor (CAR) T-Cell and Adoptive T-Cell Therapies for various cancers; and G protein-coupled receptor targets for treating immunologic, immuno-oncologic, metabolic, CNS, cardiovascular, musculoskeletal, and other disorders. The company was incorporated in 1994 and is headquartered in Seattle, Washington.