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OMER (Common Stock)
ExchangeNASDAQ (US Dollar)
Change (%) Stock is Down 1.03 (5.29%)
Data as of 06/21/18 4:00 p.m. ET
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Recent Press ReleasesMore >>
05/24/18Omeros Announces Settlement of Infringement Suit Against ANDA Filer Lupin
--Lupin Confirms Validity of OMIDRIA Patents-- SEATTLE--(BUSINESS WIRE)--May 24, 2018-- Omeros Corporation (Nasdaq: OMER) today announced that it has entered into a settlement agreement with Lupin Ltd. and its subsidiary Lupin Pharmaceuticals, Inc. (Lupin), resolving Omeros’ patent litigation against Lupin. The litigation concerned Lupin’s filing of an Abbreviated New Drug Application (ANDA) seeking approval from the U.S. Food and Drug Adminis... 
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05/10/18Omeros Corporation Reports First Quarter 2018 Financial Results
– Conference Call Today at 4:30 p.m. ET – SEATTLE--(BUSINESS WIRE)--May 10, 2018-- Omeros Corporation (NASDAQ: OMER) today announced recent highlights and developments as well as financial results for the first quarter ended March 31, 2018, which include: 1Q 2018 total and OMIDRIA® revenues were $1.6 million, compared to $12.3 million in 1Q 2017; the decrease is the result of the scheduled expiration of OMIDRIA pass-throu... 
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05/07/18Omeros Corporation to Announce First Quarter 2018 Financial Results on May 10, 2018
SEATTLE--(BUSINESS WIRE)--May 7, 2018-- Omeros Corporation (NASDAQ: OMER) today announced that the company will issue its first quarter 2018 financial results for the period ended March 31, 2018, on Thursday, May 10, 2018, after the market closes. Omeros management will host a conference call and webcast that day at 4:30 p.m. Eastern Time (1:30 p.m. Pacific Time) to discuss the financial results. Conference Call Details To a... 
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04/26/18FDA Grants Breakthrough Therapy Designation to Omeros’ MASP-2 Inhibitor OMS721 for the Treatment of High-Risk Hematopoietic Stem Cell Transplant-Associated Thrombotic Microangiopathy
– Discussions Ongoing with FDA and European Regulators for Expedited Approval – SEATTLE--(BUSINESS WIRE)--Apr. 26, 2018-- Omeros Corporation (NASDAQ: OMER) today announced that the U.S. Food and Drug Administration (FDA) has granted breakthrough therapy designation to OMS721 for the treatment of patients with high-risk hematopoietic stem cell transplant-associated thrombotic microangiopathy (HSCT-TMA), specifically those patients who have pers... 
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