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24.06.25 - 14:33
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Omeros Announces Webcast Details for Annual Meeting of Shareholders (Business Wire)
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SEATTLE--(BUSINESS WIRE)--Omeros Corporation (Nasdaq: OMER) today announced that the company will host a live webcast of its Annual Meeting of Shareholders, which will be held virtually on Friday, June 27, 2025, starting at 10:00 a.m. Pacific Time.
The live webcast can be accessed through the virtual shareholder meeting website at www.virtualshareholdermeeting.com/OMER2025. A general corporate overview and question-and-answer session will follow the business portion of the annual meeting.
As described in the Company's proxy statement, filed May 30, 2025, only shareholders of record as of the close of business on May 23, 2025 are entitled to vote at the Annual Meeting of Shareholders and any adjournment or postponement thereof. Shareholders of record will be able to attend the meeting, vote and submit questions via the virtual shareholder meeting website using the 16-digit control number provided in their proxy card or in the instructions accompanying their proxy materials.
Guests without a 16-digit contr...
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15.05.25 - 22:06
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Omeros Corporation Reports First Quarter 2025 Financial Results (Business Wire)
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– Conference Call Today at 4:30 p.m. ET
SEATTLE--(BUSINESS WIRE)--Omeros Corporation (Nasdaq: OMER) today announced recent highlights and developments as well as financial results for the first quarter ended March 31, 2025, which include:
Net loss for the first quarter of 2025 was $33.5 million, or $0.58 per share, compared to a net loss of $37.2 million, or $0.63 per share for the first quarter of 2024.
At March 31, 2025, we had $52.4 million of cash and short-term investments available for operations and debt servicing, a decrease of $37.7 million from December 31, 2024.
In March 2025, we resubmitted to the U.S. Food and Drug Administration (“FDA”) our Biologics License Application (“BLA”) seeking regulatory approval for narsoplimab in hematopoietic stem cell transplant-associated thrombotic microangiopathy (“TA-TMA”). FDA accepted the resubmission for review as a class 2 resubmission and, pursuant to the Prescription Drug User Fee Act (“PDUFA”), assigned a target date for FDA action o...
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