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ALK202 is a proprietary bispecific antibody-drug conjugate (ADC) developed by Shanghai Allink Biotherapeutics for the treatment of advanced solid tumors. It targets both the epidermal growth factor receptor (EGFR) and hepatocyte growth factor receptor (c-MET), two proteins frequently implicated in tumor progression, metastasis, and resistance to single-target therapies. By simultaneously inhibiting EGFR and c-MET, ALK202 aims to overcome resistance mechanisms associated with monotherapies and enhance antitumor efficacy. The ADC incorporates a topoisomerase inhibitor payload and utilizes common light chain technology to prevent mispairing during antibody assembly, optimizing binding affinities while reducing target-related toxicities. As of early 2025, ALK202 is being evaluated in global Phase I clinical trials for patients with advanced solid tumors who have progressed on standard therapies[1][2][3][4][5].
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