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Thursday, January 9, 2025

PureTech Receives FDA Fast Track Designation for LYT-200 in Acute Myeloid Leukemia

 Single agent and combination data from Phase 1b AML/MDS trial presented at ASH 2024 showed potential of LYT-200 to serve broad range of patients across various lines of treatment

LYT-200 is currently being evaluated in two Phase 1/2 trials for the potential treatment of AML/MDS and head and neck cancers

https://www.businesswire.com/news/home/20250109191836/en/

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