TuHURA Biosciences Inc. has filed an Investigational New Drug $(IND)$ application with the U.S. Food and Drug Administration (FDA) for its novel VISTA inhibiting antibody, TBS-2025, to be studied in combination with a menin inhibitor for the treatment of mutNPM1 relapsed/refractory acute myeloid leukemia (AML). The company plans to initiate a Phase 2 study pending FDA review and clearance.
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. Tuhura Biosciences Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: 202602170745PR_NEWS_USPR_____LA88957) on February 17, 2026, and is solely responsible for the information contained therein.