Our Piplines
Two promising therapeutic programs designed to meaningfully improve outcomes for patients
We Develop Targeted Antibody
Therapeutics That Traffic to
Specific Subcellular Organelles in Disease Tissues
LSB-T06
LSB-T06 emerged from LifeSpring Biotech’s macrophage-focused discovery platform designed to pinpoint key regulators of macrophage activation in immunosuppressive tumor microenvironments. LSB-T06 is an intracellular protein largely restricted to myeloid cell populations.
Inhibiting LSB-T06 triggers robust activation of the TLR–MyD88 signaling pathway, driving increased production of pro-inflammatory cytokines such as TNFα, IL-12, and IL-6. This immune activation occurs predominantly within the tumor microenvironment, significantly reducing systemic exposure and offering advantages over conventional systemic TLR–MyD88 agonists.
The LSB-T06 program is currently in the Hit-to-Lead stage, with several high-potency, highly selective compound families advancing in parallel.
LSB-T02
LSB-T02 is a newly characterized plasma-membrane glycoprotein primarily expressed on mucosal epithelial cells. Initially identified as an “LSB signal” during a CRISPRa-based tumor screen, the protein is believed to influence both cell adhesion and suppression of myeloid cell activity.
LSB-T02 is notably overexpressed across several major cancer types—including colorectal, gastric, liver, pancreatic, cervical, and testicular tumors—and has been linked to malignant progression in multiple solid cancers. Importantly, its expression patterns correlate with disease trajectory, underscoring its potential biological and therapeutic relevance.
LSB301
LSB301 is LifeSpring Biotech’s leading clinical development candidate—an advanced antibody-drug conjugate (ADC) built from an afucosylated monoclonal antibody directed against the novel target LSB-T02, paired with a clinically proven linker-payload system.
LSB301 is currently undergoing comprehensive preclinical pharmacology and toxicology evaluation. In parallel, LifeSpring Biotech has initiated CMC process development and manufacturing to support an anticipated Investigational New Drug (IND) submission in mid-2026.
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Our scaffolds override subcellular trafficking patterns for a target and improve ADC delivery to the lysosome. Reach out to learn more.
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