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ALK202

Development stage
Phase 2
Lead developer
Allink Biotherapeutics
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

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].

Other names
ALK 202ALK202ALK-202
02

Targets

MET (Mesenchymal-epithelial transition factor receptor)EGFR T790M (Epidermal growth factor receptor T790M mutant)

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