Huaota has independently developed the HOTAC™ (Huaota Optimized Technology of Antibody Conjugate) ADC platform, a comprehensive technology system encompassing four core modules—antibody, linker, conjugation technology, and payload. The company holds complete independent intellectual property rights across the entire ADC development chain.
Antibody Module: The platform flexibly incorporates monoclonal antibodies and nanobodies to develop multi-epitope/multispecific antibodies. Through affinity optimization, antibodies are endowed with superior antigen specificity and synergistic effects, expanding the boundaries of ADC molecular design.
Linker Module: Our proprietary linkers are specifically cleaved by cathepsin B or β-glucuronidase, enabling conditional release within the tumor microenvironment. They combine high hydrophilicity with excellent plasma stability, remaining stable in circulation and releasing the cytotoxic payload only within tumor cells, thereby minimizing off-target toxicity to normal cells.
Conjugation Technology Module: The platform has established a diverse conjugation system covering cysteine-based random/site-specific conjugation and glycan-directed site-specific conjugation, achieving highly homogeneous products. By integrating multiple conjugation technologies, we have innovatively developed dual-payload ADC technology.
Payload Module: We have developed a diversified next-generation toxin payload portfolio, including novel topoisomerase I inhibitors and first-in-class payloads (N-myristoyltransferase inhibitors, DNA damage repair inhibitors, molecular glues, etc.). Our proprietary payloads exhibit enhanced bystander killing effects and cell membrane permeability, effectively overcoming tumor resistance.
Leveraging a differentiated next-generation payload portfolio, we mitigate the risk of resistance commonly associated with existing ADC drugs. The HOTAC™ platform works in deep synergy with the company's AI-assisted, structure-based innovative monoclonal/multispecific antibody discovery platform, continuously generating ADC candidates with clinical trial application potential.