Cullinan Therapeutics Inc. has announced updated clinical data from its Phase 1 study of CLN-049, a novel FLT3xCD3 bispecific T cell engager, in patients with relapsed or refractory acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS). The results, which include a 31% CR/CRh rate at the highest target dose tested and a favorable safety profile across all doses, were presented as an oral presentation at the 67th American Society of Hematology $(ASH)$ Annual Meeting and Exposition on December 8, 2025. CLN-049 has recently been granted Fast Track designation by the U.S. FDA, and dose escalation in the ongoing Phase 1 study continues, with expansion cohorts planned for early 2026.
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. Cullinan Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9597902-en) on December 08, 2025, and is solely responsible for the information contained therein.
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