Omeros Corporation announced the successful completion of an initial nonhuman primate study evaluating its OncotoX-AML therapeutic platform for acute myeloid leukemia (AML). The study demonstrated a marked, selective, and reversible reduction in myeloid progenitor cells, with OncotoX-AML being well tolerated and showing no significant safety signals. In preclinical murine-human xenograft models, OncotoX-AML also showed superior efficacy compared to standard-of-care treatments. The results from these studies have already been presented, and Omeros plans to initiate IND-enabling studies to advance OncotoX-AML toward clinical trials, targeting a first-in-human trial in late 2027.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Omeros Corporation published the original content used to generate this news brief via Business Wire (Ref. ID: 202602170845BIZWIRE_USPR_____20260217_BW464206) on February 17, 2026, and is solely responsible for the information contained therein.
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