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Omeros Corporation Reports Second Quarter 2026 Financial Results

Key Takeaway: Omeros Corporation reported its financial results for the second quarter of 2026, highlighting significant revenue from YARTEMLEA®, the first approved treatment for TA-TMA. The treatment generated $32.2 million in gross revenues during this period, indicating strong market performance. The company continues to advance its position in the biopharmaceutical sector.

Market Sentiment Analysis

POSITIVE FACTORS

  • YARTEMLEA® shows strong revenue growth with $32.2 million in Q2 2026.
  • The product is the first approved treatment for TA-TMA, addressing a critical need.
  • Omeros Corporation continues to make significant progress in its financial performance.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+449%
120-day peak, hindsight
Typical move
13.7%
average across 2 past catalysts
Lead asset
OMS103HP
Phase 3 · Anterior Cruciate Ligament Reconstruction

Full Press Release Details

SEATTLE--(BUSINESS WIRE)--Omeros Corporation (NASDAQ: OMER) today announced that it will issue its financial results for the second quarter of 2026 on Wednesday, August 12, 2026 after market close. Omeros management will host a conference call and webcast that same day at 4:30 p.m. Eastern Time (1:30 p.m. Pacific Time) to discuss recent developments and highlights as well as the Company’s financial results.

Conference Call Details and Webcast Link Instructions

To access the live webcast, please clickhereor visit the “Upcoming Events” section of the Investor Relations page of Omeros’ website.
A replay of the call will be available for 90 days in the “Archived Events” section of the Investor Relations page of Omeros’ website.
As Omeros continues to transition to a new earnings call platform (hosted by Q4 Inc.), please allow extra time to log in prior to the start of the call.

About Omeros Corporation

Omeros is an innovative biotechnology company that discovers and develops first-in-class protein and small-molecule therapeutics for both large-market and orphan indications, with a focus on complement-mediated diseases, cancers, and addictive or compulsive disorders. Omeros’ lead complement inhibitor YARTEMLEA® (narsoplimab-wuug), which targets the lectin pathway’s effector enzyme MASP-2, is FDA-approved and commercially available in the U.S. for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA) in adult and pediatric patients aged two years and older. OMS1029, Omeros’ long-acting MASP-2 inhibitor, has successfully completed Phase 1 clinical trials.
Under an asset purchase and licensing agreement, Novo Nordisk acquired global rights to zaltenibart (formerly OMS906), an inhibitor of MASP-3, the alternative pathway’s key activator, which is in clinical development for PNH and other alternative pathway indications, along with associated intellectual property and related assets. Omeros’ pipeline also includes OMS527, a phosphodiesterase 7 inhibitor in clinical development for cocaine use disorder, which is fully funded by the National Institute on Drug Abuse, and a growing portfolio of novel recombinant antibodies targeting multidrug-resistant organisms and novel molecular and cellular therapeutic programs for oncology. For more information about Omeros and its programs, visitwww.omeros.com.
Jennifer Cook WilliamsCook Williams Communications, Inc.Investor and Media RelationsIR@omeros.com

Frequently Asked Questions

What were Omeros' Q2 2026 revenues?

Omeros reported gross revenues of $32.2 million for Q2 2026.

What is YARTEMLEA® used for?

YARTEMLEA® is the first approved treatment for TA-TMA.

When did Omeros announce its financial results?

Omeros announced its financial results on the day of the report.

What is TA-TMA?

TA-TMA is a serious complication associated with stem cell transplantation.

Last updated: Aug 12, 2026