Preclinical pharmacokinetic modeling and clinical translation of SIG001, a novel anti-cancer therapeutic antibody targeting on cancer-derived sialylated IgG.

Introduction: Sialylated immunoglobulin G (SIA-IgG) has emerged as a novel therapeutic target selectively overexpressed in epithelial-derived malignancies. The humanized monoclonal antibody SIG001 binds specifically to tumor-associated SIA-IgG and is regarded as a promising first-in-class candidate for the broad-spectrum treatment of epithelial cancers. Methods: The pharmacokinetic (PK) behavior of SIG001 was evaluated in both cynomolgus monkeys and mice following intravenous administration. Utilizing modeling approaches, we projected the first-in-human (FIH) starting dose and the human pharmacologically active dose (PAD) from preclinical datasets. Results: In cynomolgus monkeys, single-dose PK was assessed at 5, 15, and 30 mg/kg, while in mice, doses of 5, 10, and 20 mg/kg were investigated. Data from both species were well characterized by a two-compartment model with linear elimination kinetics; human PK parameters were extrapolated from the monkey studies. Conclusion: The preclinical investigations delineate the PK profile and antitumor activity of SIG001. The quantitative translation of animal data into human PK and exposure-response expectations provides a rational foundation for clinical development and supports informed decision-making in the design of early-phase trials.