Amended: Omeros Eyes Dec.26 FDA Decision On Narsoplimab For TA-TMA

Amended: The article, posted on September 17, 2025, about Omeros Corp. (OMER) incorrectly mentioned the PDUFA date as September 25, 2025.

Omeros Corp. (OMER) is approaching a pivotal regulatory milestone as the FDA prepares to issue its decision on the Biologics License Application (BLA) for narsoplimab, the company's lead investigational therapy. The FDA has assigned a PDUFA target action date of December 26, 2025, for its review of narsoplimab in the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy/TA-TMA.

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by RTTNews Staff Writer

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