$3.83
Omeros


Performance
Dividends
1W
1M
YTD
1Y
3Y
8/36
Growth
Score
12/36
Dividend
Score
Valuation
PE Ratio
-1.45
PS Ratio
544
RSI
-
PEG Ratio
0.18
PRG Ratio
0
0
PDG Ratio
0
Growth
2023
2024
2025*
2026*
3
Revenue
Revenue
*Analyst estimated growth
Fundamentals
Rule
of 40
-95.91%
Gross Margin
-50.49%
1
Current Ratio
1.16
Return on Assets
-65.1%
3
Return on Equity
90.73%
0
Return on inv. Capital
-104.56%
Institutional Holder
Shares
Holders
Financials
Yealy
Quarterly
Revenue 2024 0
2018
2019
2020
2021
2022
2023
2024
6
Net Income 2024 -156.81M
2018
2019
2020
2021
2022
2023
2024
6
Gross Profit 2024 0
2018
2019
2020
2021
2022
2023
2024
6
Events

OMER
Omeros
in 287 days
after market close
Earnings per Share is expected with - and revenue with - .

OMER
Omeros
in 243 days
after market close
Earnings per Share is expected with - and revenue with - .

OMER
Omeros
in 104 days
after market close
Earnings per Share is expected with - and revenue with - .
About
Sector/Industry
Healthcare
Biotechnology
IPO Date
08.10.2009
MaketCap
224.41M
Country
US
CEO
Gregory A. Demopulos
Description
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.
Updated 28.07.2025