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Latticon Biopharmaceuticals

Gaithersburg, Maryland, United States
Ownership
Private
Development stage
Phase 1
01

Overview

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.

Therapeutic areas
Oncology
Modalities
Antibody-based therapiesImmunocytokines (antibody-cytokine fusion proteins)
Industry
Biotech
02

Partnerships

Zencore Biologics – CMC/CDMO services provider supporting IND-enabling work for LAT010Laitekang (Suzhou) – Clinical development partner in ChinaNo major pharma partnerships publicly disclosed.

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