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Omeros Announces Upcoming Presentation at EBMT 2026 Highlighting Advances in TA-TMA Treatment

Key Takeaway: Omeros Corporation announced its participation in the upcoming EBMT 2026 meeting, where it will host a session on advances in TA-TMA treatment. The session will be co-chaired by notable experts and feature discussions on novel targeted therapies. Omeros continues to develop innovative treatments, including its FDA-approved product YARTEMLEA for TA-TMA.

Market Sentiment Analysis

POSITIVE FACTORS

  • Omeros will present at a significant industry event, EBMT 2026.
  • The session will focus on novel therapies for TA-TMA treatment.
  • Omeros' lead product, YARTEMLEA, is FDA-approved and available in the U.S.
  • The company has a promising pipeline with ongoing clinical developments.

Full Press Release Details

SEATTLE--(BUSINESS WIRE)--Omeros Corporation (NASDAQ: OMER) today announced that it will host an industry session at the 52ndAnnual Meeting of the European Society for Blood and Marrow Transplantation (EBMT) on March 22, 2026, from 2:30pm - 4pm CET in Madrid, Spain. The session, titled“Advances in TA-TMA Treatment: Evaluating the Role of a Novel Targeted Therapy,”will be co-chaired by Rafael Duarte, MD, PhD, Hospital Universitario Puerta de Hierro Majadahonda, and Mohamad Mohty, MD, PhD, Hôpital Saint-Antoine, AP-HP, and will feature speakers Miguel-Angel Perales, MD, Memorial Sloan Kettering Cancer Center, and Michelle L. Schoettler, MD, MS, Children’s Healthcare of Atlanta.
The EBMT Annual Meeting is a key event for professionals in transplantation and cellular therapy, bringing together stakeholders from around the world.
About Omeros Corporation
Omeros is an innovative, commercial-stage biotechnology company that discovers and develops first-in-class protein and small-molecule therapeutics for large-market and orphan indications, with particular emphasis on complement-mediated diseases, cancers, and addictive or compulsive disorders. Omeros’ lead lectin pathway inhibitor YARTEMLEA®(narsoplimab-wuug), which inhibits the 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. A marketing authorization application for YARTEMLEA in TA-TMA is currently under review at the European Medicines Agency. OMS1029, Omeros’ long-acting MASP-2 inhibitor, has successfully completed Phase 1 clinical trials.
Under a recently announced asset purchase and licensing agreement, Novo Nordisk acquired global rights to zaltenibart (formerly OMS906), a MASP-3 inhibitor 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 that is fully funded by the National Institute on Drug Abuse, as well as a growing portfolio of novel molecular and cellular oncology programs. 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 is the focus of Omeros' presentation at EBMT 2026?

Omeros will focus on advances in TA-TMA treatment, evaluating a novel targeted therapy.

Who will co-chair the session at EBMT 2026?

The session will be co-chaired by Rafael Duarte and Mohamad Mohty.

What is YARTEMLEA used for?

YARTEMLEA is FDA-approved for treating TA-TMA in adult and pediatric patients.

Where is the EBMT 2026 meeting taking place?

The EBMT 2026 meeting will be held in Madrid, Spain.

Last updated: Mar 23, 2026