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AMX0318 selected as development candidate after meeting key criteria, demonstrating a robust chemical stability profile, strong in vitro potency, evidence of in vivo efficacy and tolerability, high solubility, and a favorable pharmacokinetic profile consistent with a long-acting peptide IND-enabling studies expected to initiate in 2026 with an IND targeted for 2027, pending successful completion of IND-enabling studies CAMBRIDGE, Mass

In addition, due to its selective effect on bad cells, SAG is emerging as a promising new substance for lymphoma patients since it increases cell apoptosis

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