Drug intelligence / Profile preview

LK101 + tislelizumab

Development stage
Phase 2
Lead developer
Likang Life Sciences Holdings
Modality
Dendritic Cell Vaccines → Immune Effector Cells → Other Cell Types → Cell Therapies, Vaccines & Immunotherapeutics, mRNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intradermal, Intravenous
01

Overview

LK101 + tislelizumab is an investigational combination immunotherapy consisting of LK101, a personalized neoantigen-targeted mRNA-loaded dendritic cell (DC) vaccine, and tislelizumab (Tevimbra), a humanized IgG4 monoclonal antibody targeting programmed cell death protein 1 (PD-1). Developed by Likang Life Sciences in collaboration with BeiGene, the combination is designed to synergistically enhance anti-tumor immune responses. LK101 is custom-manufactured for each patient by transfecting autologous dendritic cells with mRNA encoding up to 30 patient-specific tumor neoantigens, which primes neoantigen-specific T-cell responses. Tislelizumab blocks the interaction of PD-1 with its ligands PD-L1 and PD-L2, thereby relieving T-cell inhibition. The combination is primarily being evaluated as a first-line maintenance therapy for patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) and extensive-stage small cell lung cancer (ES-SCLC).

Other names
LK101 + BGB-A317LK101 + TevimbraLK101 + tislelizumab-jsgrLK101 injection + tislelizumabLK101 plus tislelizumabLK-101 plus tislelizumabLK 101 plus tislelizumab
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)CD274 (Programmed cell death protein 1 ligand 1)PDCD1LG2 (Programmed cell death 1 ligand 2)γδ TCR (T-cell receptor)pMHC-I (Peptide–MHC class I complex)

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