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Latticon is conducting a first-in-human, open-label, multicenter Phase 1/2 trial of its lead program LAT010 in patients with advanced solid tumors. The study aims to evaluate safety, tolerability, immunogenicity, pharmacokinetics/pharmacodynamics and preliminary efficacy. The IND for LAT010 was approved by the FDA in late 2023; as of early 2025 the trial is actively recruiting and no topline results have been reported yet.
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