Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
LM-299 is an investigational bispecific antibody designed to target both programmed cell death protein-1 (PD-1) and vascular endothelial growth factor (VEGF). By simultaneously inhibiting the PD-1/PD-L1 immune checkpoint pathway and the VEGF/VEGFR angiogenesis pathway, LM-299 aims to enhance anti-tumor immunity while suppressing tumor blood vessel formation. The molecule features a differentiated design with an anti-VEGF antibody linked to two C-terminal single domain anti-PD-1 antibodies. Developed initially by LaNova Medicines Ltd., Merck has acquired exclusive global rights for its development, manufacturing, and commercialization. As of late 2024, LM-299 is in Phase 2 clinical trials for advanced solid tumors in China, with plans for further trials in the United States[1][2][3][5][6].
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on LM-299.